The Korean Association for the Study of the Liver (KASL): KASL Clinical Practice Guidelines: Management of chronic hepatitis B
The guideline on the management of chronic hepatitis B (CHB) was first developed in 2004 and revised in 2007 by the Korean Association for the Study of the Liver (KASL). Since then there have been many developments, including the introduction of new antiviral agents and the publications of many novel research results from both Korea and other countries. In particular, a large amount of knowledge on antiviral resistance-which is a serious issue in Korea-has accumulated, which has led to new strategies being suggested. This prompted the new guideline discussed herein to be developed based on recent evidence and expert opinion.
The main targets of this guideline comprise patients who are newly diagnosed with CHB and those who are followed or treated for known CHB. This guideline is also intended to provide guidance for the management of patients under the following special circumstances: malignancy, transplantation, dialysis, coinfection with other viruses, pregnancy, and children.
This revised CHB guideline is designed as resource for all Korean clinicians caring for patients with CHB. It also provides physicians in training courses with practical information on the management of CHB.
Developer and funding source
The CHB Clinical Practice Guideline Revision Committee (CPGRC) comprising 15 hepatologists and 1 pediatrician was formed with support from KASL (Appendix 2
). All of the required funding was provided by KASL. Each member of CHB-CPGRC collected and evaluated evidence, and contributed to writing the manuscript. Conflicts of interests of the CHB-CPGRC members are summarized in Appendix 1
Relevant evidence obtained in a comprehensive literature search using MEDLINE (up to 2011) was systematically reviewed and selected. The literature languages were limited to English and Korean. In addition to published articles, abstracts of important meetings published before 2011 were also evaluated. The following search terms were used: "hepatitis B", "hepatitis B virus", "HBV", "chronic hepatitis", and other key words related to clinical questions (see below). These clinical questions covered a variety of pertinent topics ranging from epidemiology, natural course, and prevention to diagnosis, treatment, antiviral resistance, and special situations.
Levels of evidence and grades of recommendation
The evidences and recommendations were graded according to the GRADE system (Grading of Recommendations, Assessment, Development and Evaluation) with minor modifications.1
) The levels of evidences were determined by the possibility of change in the estimate of clinical effect by further research, and were described as high (A), moderate (B) or low (C). The grades of recommendation were either strong (1) or weak (2), as determinted by the quality of evidence as well as patient-important outcomes and socioeconomic aspects.
List of the clinical questions
The committee considered the following questions as key components to be covered in this guideline.
How does this guideline differ from previous guidelines?
What is the updated knowledge on the epidemiology and natural course?
How should the infection be prevented?
How are the patients evaluated prior to treatment?
When should treatment be considered?
What are the goals and endpoints of treatment?
What are the optimal first-line treatments for different disease status?
How should the treatment be monitored?
When can we consider stopping treatment?
What are the predictors of the treatment response?
What are the definitions of treatment failure, antiviral resistance, and recurrence after treatment completion, and how should these aspects be managed?
How should the following special groups be managed: acute hepatitis B, liver transplantation, chemotherapy/immunosuppression, renal failure, coinfection [with hepatitis C virus (HCV), hepatitis D virus (HDV), and/or human immunodeficiency virus (HIV)], pregnancy, and children?
Review of the manuscript
Drafts of the revised guideline were thoroughly reviewed at six separate meetings of the committee. In addition to the contents, methodological validity was also assessed according to the AGREE II (Appraisal of Guidelines for Research and Evaluation II) instrument.5
A revised manuscript was reviewed at a meeting of an external review board, and at a symposium open to all KASL members, and was modified further prior to publication. The external review board comprised of 12 specialists on CHB who are members of KASL. The final manuscript was endorsed by the board of executives of KASL (see Appendix 2
Plan for updates
Updates or full revision will be planned when new major evidences are accumulated in diagnosis and/or treatment of CHB. Detailed plans for updates will be posted on the KASL webside later.
Hepatitis B infection is a major etiology of acute and chronic hepatitis, cirrhosis, and hepatocellular carcinoma (HCC). It has been recognized as an important public health problem in Korea since the 1970s,7
and was designated as a third-class infectious disease by law in 1982. Hepatitis B infection is currently classified as one of the second group of infectious disease designated by law and is addressed by national vaccination programs.8
The prevalence of HBV infection in the Korean population as estimated by positivity rates for hepatitis B surface antigen (HBsAg) was 8-9% for males and 5-6% for females during the early 1980s.9
Thereafter the prevalence of HBV infection tended to decline gradually due to the initiation of a vaccination program for newborn infants in 1991 and a national vaccination program in 1995. For example, the prevalence of HBV among children aged 4 to 6 years had decreased to 0.2% in 2006.10
Nevertheless, according to the 2005 Korean National Health and Nutrition Examination Survey, the positivity rate for HBsAg among people aged 10 years or older was 4.8% for males and 3.0% for females, with 3.7% of the total population being infected with HBV.11
Positivity rates for HBsAg among pregnant women-who represent a major infection route for hepatitis B-declined during the 1980s but remained stagnant during the 1990s. Perinatal infection rates of HBV have not decreased, being 3.4% in 1995 and 3.2% in 2006; moreover, the incidence of sporadic acute hepatitis B infection has been increasing since 2001.11
Given that HBsAg is detected in approximately 70% of patients with chronic hepatitis or cirrhosis,12
and in 65-75% of HCC patients,13
it can be concluded that CHB infection still greatly affects public health in Korea.
Most Korean CHB patients are infected with HBV subgenotype C215
; these patients are known to have lower hepatitis B e antigen (HBeAg) seroconversion rates, more rapidly progress to HCC and cirrhosis, lower interferon treatment effects, and are subject to have higher rates of relapse after antiviral treatments, compared to those infected with other HBV genotypes.16
Natural History of CHB
The progression of CHB may be divided into five clinical phases: immune-tolerant phase, immune-reactive phase, inactive HBV-carrier phase, HBeAg-negative CHB phase, and HBsAg-clearance phase. Individual patients do not necessarily experience different clinical stages in a continuous manner.18
The five phases have the following characteristics:
1) The "immune tolerant" phase
In cases of perinatal infection, the immune-tolerant phase is characterized by HBeAg positivity, high levels of serum HBV DNA (generally ≥107
IU/mL), normal levels of aspartate aminotransferase/alanine aminotransferase (AST/ALT), and mild or no liver necroinflammation.20
This phase may continue for longer than 3 decades in those infected with HBV genotype C, which is common among Korean patients, and the rate of spontaneous HBeAg loss is very low.23
Therefore, many women infected with this genotype are in the HBeAg-positive immune-tolerant phase when they are of childbearing age. No or only mild histologic liver damage, despite high levels of HBV DNA, is attributed to immune tolerance to HBV.24
2) The "immune reactive" phase
Most patients in the immune-tolerant phase will experience immune responses against HBV as they grow older, and finally reach the immune-reactive phase that is characterized by HBeAg positivity, lower serum HBV DNA levels, and increased or fluctuating levels of ALT.25
Histologic findings in this phase include moderate-to-severe liver inflammation and, in some patients, rapid progression of fibrosis.27
Such changes are due to enhancement of HBV core antigen (HBcAg) or HBeAg-specific cytotoxic T-lymphocyte activity and the resulting destruction of infected hepatocytes.28
Sustained HBV DNA suppression occasionally accompanies HBeAg seroconversion. Once HBeAg seroconversion occurs, the natural course of the disease may have one of three clinical features: repeated HBeAg reversion and seroconversion, inactive HBV-carrier state, or HBeAg-negative CHB.29
Typically 10-40% of patients who experience seroconversion revert to HBeAg positivity and then experience the recurrence of seroconversion at least once with progression of hepatitis activity.27
In particular, reversion frequently occurs in patients with HBV genotype C, with its rates declining with age.23
3) The "inactive HBV-carrier" phase
Most patients who seroconvert during the immune-reactive phase progress to the inactive HBV-carrier phase, which is characterized by HBeAg negativity, persistent normal ALT levels, and HBV DNA levels of less than 2,000 IU/mL.33
Typical histologic findings of this phase are mild liver inflammation and fibrosis;33
however, patients who have suffered from previous severe inflammation and fibrosis may continue to experience moderate-to-severe inflammation and fibrosis. This may result in even biochemical and histologic tests not being useful for differentiating these patients from those with cirrhosis who require antiviral treatment.34
This phase persists for a long time in most patients, but with a relatively good prognosis; however, an estimated 20% of them will reactivate to the HBeAg-negative or HBeAg-positive immune-reactive phase, and they might experience recurring periods of reactivation and inactivation throughout their lives, which can lead to cirrhosis or HCC.36
This is why the ALT levels of patients in the inactive HBV phase must be followed every 6 months for life because currently there are no predictors for whom will remain in the inactive phase or revert to HBeAg-negative active hepatitis.19
4) The "HBeAg negative CHB" phase
Approximately 20% of patients who experience HBeAg seroconversion during their immune-reactive phase maintain HBeAg negativity and hepatitis B e antibody (anti-HBe) positivity but progress to HBeAg-negative CHB, with findings of HBV DNA levels of 2,000 IU/mL or higher, increased levels of ALT, and active liver necroinflammation.29
These patients show HBeAg negativity since they harbor HBV variants in the precore (PC) or basal core promoter (BCP) regions of HBV DNA, resulting in a failure to generate HBeAg.38
HBeAg-negative CHB is associated with low rates of prolonged spontaneous disease remission, and most patients in this phase will experience persistent hepatocellular inflammation and progress to hepatic fibrosis and cirrhosis.40
Severe fluctuations of HBV DNA and ALT levels sometimes make it difficult to differentiate these patients from those in the inactive HBV-carrier phase.42
Accordingly, for the first year after a patient is diagnosed as being in the inactive HBV-carrier phase, HBV DNA and ALT levels should be measured every 3 months in order to differentiate HBeAg-negative CHB patients who need antiviral treatment.19
5) The "HBsAg-clearance" phase
Patients in the inactive HBV-carrier phase subsequently experience the HBsAg clearance phase at a rate of 1-2% annually. HBsAg loss occurs42
regardless of the patient's gender and virus genotype, with age being the only known influencing factor.46
It has been reported that Korean patients experience a relatively low rate of HBsAg loss (0.4% annually).48
HBV DNA is not detectable in the serum during this phase, while hepatitis B core antibody (anti-HBc) with or without hepatitis B surface antibody (anti-HBs) are detectable. HBsAg loss is known to be associated with a reduced risk of cirrhosis but a sustained significant risk of HCC development.36
Risk Factors that Influence the Natural History of CHB
The accumulated incidence of cirrhosis developing from CHB is generally reported to be 8-20%.55
In Korea the reported annual and 5-year accumulated incidences of cirrhosis are 5.1% and 23%, respectively, while those for HCC are 0.8% and 3%.56
The risk factors for chronic hepatitis B progressing to cirrhosis or HCC can be divided into demographic, environmental, social, and viral factors (Table 2
Regarding demographic factors, the risk of developing HCC is three- to fourfold higher for men than for women, and the risk of HCC and cirrhosis is low among those younger than 40 years then increases exponentially with increasing age after the fourth decade of life.27
Those with a family history of HCC also have a higher risk of HCC development.60
Environmental and social risk factors for the progression to cirrhosis or HCC are alcohol consumption, exposure to aflatoxin,62
It remains controversial whether obesity, metabolic syndrome, and fatty changes in histologic tests increase the risk of CHB patients progressing to hepatic fibrosis or HCC.64
Many epidemiological research studies have found that coffee exerts protective effects against the development of hepatic fibrosis and HCC.68
Although there are no research reports on the role of coffee in hepatitis B patients, coffee may be protective in HBV since multiple studies have shown coffee intake to be protective in various liver diseases.
Viral factors that may influence the progression of CHB patients to cirrhosis or HCC include high levels of serum HBV DNA (≥20,000 IU/mL), genotype C, BCP variants, and coinfection with other viruses.73
According to the Taiwanese REVEAL-HBV (Risk Evaluation of Viral Load Elevation and Association Liver Disease/Cancer-Hepatitis B Virus) study, the risk of developing HCC during the study period among subjects aged at least 40 years was significantly higher in those with an HBV DNA level of ≥104
copies/mL (cpm) at the start of observation and 105
cpm 11 years later than among those with an entry HBV DNA level of <104
Likewise, the incidence of cirrhosis was found to be significantly associated with HBV DNA levels higher than 104
cpm at study entry. When the HBV DNA level decreased during the follow-up period, the risk of developing HCC or cirrhosis reduced. Subsequent research highlighted the clinical importance of very careful evaluation of patients with an HBV DNA level of higher than 2,000 IU/mL who are older than 40 years (especially those who still have HBeAg positivity) for the development of fibrosis76
and intervention with antiviral therapy when appropriate, as recommended by established practice guidelines.57
Unlike HCV infection, the HBV genotype exerts a profound effect on the clinical outcome but-with the exception of interferon-little effect on the treatment outcome.78
Eight HBV genotypes have been identified, and that with the worst prognosis is known to be genotype C, which is the most common in Korean CHB patients.79
According to a cohort study in Alaska, hepatitis B patients with genotype A-, B-, and D-infections typically experience seroconversion from HBeAg to anti-HBe before they reach the age of 20 years, whereas in those infected with the genotype C this occurs at a mean age of 47 years.23
This implies that those infected with the genotype C would on average experience a much longer period of infection with high viral loads of HBV. This may partially explain why the risks of HCC and cirrhosis are so high in patients infected with genotype C. Two important genetic mutations of HBV that affect the natural history of CHB infection are BCP and PC mutations.43
BCP mutations are A1762T and G1764A mutations in the HBV BCP regions, and multiple cross-sectional or prospective studies have indicated that they increase the risks of cirrhosis and HCC development.43
According to the results of the REVEAL-HBV study, 359 and 1,149 individuals out of a population of 100,000 developed HCC without and with BCP mutations, respectively.82
PC mutation typically appears near the time of HBeAg seroconversion. The mutation results in an amino-acid change that creates a stop codon at site 1896 on the HBV genome, which results in the virus being able to transcribe hepatitis B core protein but not HBeAg.46
Patients infected with PC mutants are characterized by HBeAg negativity and HBeAg positivity, but high levels of HBV DNA.83
However, the observed effects of PC mutants on the natural history of CHB have been inconsistent; a recent analysis of the role of PC in the prospective population-based REVEAL-HBV study revealed the opposite to what was found in cross-sectional clinic-based studies-that the presence or absence of the PC mutation respectively decreased or increased the annual subsequent incidence of HCC (269 and 996 per 100,000, respectively).82
Although tests for both PC and BCP mutations are commercially available, it is premature for clinicians to place patients on antiviral therapy based on a mutational profile.57
PREVENTION OF HBV INFECTION
Because HBV infection is endemic in Korea, any person who has a high risk of liver disease or has suspected liver disease is recommended to have their HBsAg and anti-HBs statuses checked.18
There is a risk of HBV carriers infecting others, and hence they should be counseled regarding how to modify their lifestyle so as to prevent HBV transmission to others (Table 3
). Epidemiologic studies found that the daily consumption of 40-80 g of alcohol is associated with liver damage and the progression of liver disease,85
and a long-term prospective cohort study of HBV carriers showed that alcohol consumption increases the risks of liver cirrhosis and the development of HCC.74
No data are available on the threshold level of alcohol consumption required to significantly increase the risks of liver cirrhosis and HCC in HBV carriers. In the general population, a daily alcohol intake of 24 g in men and 12 g in women significantly increases the risk of liver cirrhosis. Therefore, abstinence or a very limited consumption of alcohol is recommended in HBV carriers.91
Smoking also increases the risks of liver cirrhosis and HCC. Therefore non-smoking is recommended in HBV carriers.74
Vertical infection is the most important route of HBV transmission. Hepatitis B immunoglobulin (HBIG) and vaccine administered after birth, followed by completion of a three-dose vaccine has been demonstrated to be 90-95% effective in preventing HBV infection in infants born to HBsAg-positive women.93
Therefore, such infants should receive 0.5 mL HBIG and HBV vaccination within 12 hours of birth. However, the introduction of HBV vaccination did not result in the rate of HBV infection among newborns differing between breast- and formula-feeding HBsAg-positive mothers (0% vs. 3%, respectively).96
Since HBV is endemic in Korea, Koreans who are negative for HBsAg and anti-HBs should be vaccinated, especially the household members and sexual partners of HBV carriers since they have an increased risk of HBV infection.93
Sexual partners who have not been tested for HBV serologic markers, have not completed the full immunization series, or who are negative for anti-HBs should use barrier protection such as condoms.
The three doses constituting the hepatitis B vaccine series administered intramuscularly at 0, 1, and 6 months induces a protective antibody response (anti-HBs >10 mIU/mL) in >90% of recipients. Most nonresponders (44-100%) subsequently respond to an additional three-dose revaccination.93
Although serologic testing for the anti-HBs response is not necessary after routine vaccination in immunocompetent adults, postvaccination testing is recommended in some subjects. The anti-HBs status of newborns of HBV-infected mothers, healthcare workers, sexual partners of HBV carriers, HIV-infected people, dialysis patients, and other immunocompromised subjects should be tested after they have completed the HBV immunization series.93
While anti-HBs levels can decline or disappear over several decades, vaccinated subjects remain protected against HBV infection and there is no need for booster vaccination in immunocompetent subjects. However, an anti-HBs level of <10 mIU/mL in dialysis patients indicates an increased risk of HBV infection. Therefore, a booster vaccination is needed if annual testing reveals an anti-HBs level of <10 mIU/mL;93
this also applies to immunocompromised patients.93
A person without protective anti-HBs exposed to HBV-contaminated blood or body fluids should receive HBIG (0.06 mL/kg) and hepatitis B vaccine as soon as possible; preferably within 24 hours, otherwise postexposure prophylaxis should be initiated within 7 days for percutaneous exposure or within 14 days for sexual exposure. Detailed recommendations for postexposure prophylaxis in both nonoccupational and occupational exposures have been developed.93
Coinfection with hepatitis A in HBV carriers increases the risk of mortality by 5.6-to 29-fold.100
Therefore, hepatitis A vaccination is recommended if they are negative for the protective hepatitis A virus antibody (anti-HAV) (Table 3
HBV vaccination is recommended in people who are negative for HBsAg and anti-HBs (A1).
Abstinence or a very limited consumption of alcohol is recommended in HBV carriers (A1).
Non-smoking is recommended in HBV carriers (A1).
Newborns of HBV-infected mothers should receive HBIG and hepatitis B vaccine at delivery and the three-dose hepatitis B vaccine (A1).
Hepatitis A vaccine is recommended for HBV carriers who are negative for anti-HAV (A1).
HBV carriers should be counseled regarding how to modify their lifestyle so as to prevent HBV transmission to others (B1).
DIAGNOSIS AND INITIAL EVALUATION
CHB refers to chronic inflammation and necrosis of the liver caused by HBV infection. CHB is defined as when HBsAg is present for longer than 6 months with a serum HBV DNA level of ≥2,000 IU/mL in HBeAg-negative CHB and ≥20,000 IU/mL in HBeAg-positive CHB and persistent or intermittent elevation of AST/ALT. The condition is divided into HBeAg-positive and -negative CHB (Table 4
The initial evaluation of CHB patients should include a thorough history-taking and physical examination, with emphasis on risk factors such as alcohol consumption or drug use, coinfection, and the family history of HBV infection and HCC. The causal relationship between HBV infection and liver disease still has to be established because not all patients with CHB have persistently elevated AST/ALT. Appropriate longitudinal long-term follow-up is crucial for patients with CHB. Serologic tests, virologic tests, biochemical tests and/or liver biopsy are used to assess HBV replication and degree of liver injury in patients with CHB (Table 5
Serologic tests including of HBsAg, anti-HBs, and anti-HBc can help when screening populations for HBV infection and for differentiating among acute, chronic, and past infections. Acute HBV infection is diagnosed by positive test results for HBsAg and immunoglobulin M (IgM) anti-HBc.102
Some people may test positive for anti-HBc but negative for HBsAg or anti-HBs. The positive finding of isolated IgM anti-HBc can occur during the window phase of acute hepatitis B,103
while the positive finding of isolated immunoglobulin G (IgG) anti-HBc can occur for the following reasons: (1) anti-HBs has decreased to an undetectable level after recovering from a previous infection, and (2) HBsAg has decreased to an undetectable level after HBV infection (occult hepatitis B).104
Measurement of the serum HBV DNA level might be helpful in these settings. Patients with these serologic patterns should be followed with repeated testing of HBsAg, anti-HBs, and anti-HBc in 3-6 months in order to detect these possibilities. By definition, patients who remain positive for HBsAg for longer than 6 months have progressed to chronic infection. Patients who recover from HBV infection will test negative for HBsAg and positive for anti-HBs and anti-HBc. Patients who respond adequately to hepatitis B vaccines will test negative for anti-HBc and positive for anti-HBs, since anti-HBc emerges only after HBV infection and persists for life.
Laboratory tests for patients with CHB should include HBeAg and anti-HBe. HBeAg positivity generally demonstrates high viral replication, while anti-HBe positivity demonstrates low viral replication.108
HBeAg-positive CHB patients are positive for HBeAg, negative for anti-HBe, and high levels of HBV DNA. They have increased levels of AST/ALT in the immune-reactive phase. The serum HBV DNA and AST/ALT levels are important in HBeAg-negative patients. HBeAg-negative, anti-HBe-positive patients with a normal ALT level and an HBV DNA level of <2,000 IU/mL (<10,000 cpm) may be in the inactive carrier state. These patients usually have mild or no liver necroinflammation and no or slow progression of fibrosis, but some patients with severe liver damage during the immune-reactive phase may present with a cirrhotic liver. HBeAg-negative CHB patients have an elevated ALT and an HBV DNA level of >2,000 IU/mL. HBe-negative CHB is associated with viral mutants in PC and/or BCP regions that are unable to produce or produce only low levels of HBeAg.41
They have severe liver necroinflammation with a low rate of prolonged spontaneous disease remission and a high risk of subsequent complications such as decompensated cirrhosis and HCC.109
The anti-HAV seroprevalence rate in Korea was 45% for the population younger than 10 years and 90-100% in the population older than 20 years during the late 1970s and early 1980s.110
However, it has declined markedly since the late 1990s due to improvements in the socioeconomic status and hygiene practices. A recent survey of Koreans who underwent medical checkups found that the anti-HAV seroprevalence rates were >90%, 50%, 10-20%, and <10% among people older than 40 years and in their 30s, 20s, and 10s, respectively.111
Similar trends have also been observed in patients with chronic liver disease.113
These trends result in increased icteric manifestation, longer recovery time, and increased risk of fulminant hepatic failure of acute hepatitis A. Many studies have found that underlying chronic liver disease is an important risk factor for fulminant hepatic failure and death in patients with acute HAV infection.114
Therefore, CHB patients younger than 50 years should undergo testing for IgG anti-HAV, and all patients with a negative immune status for hepatitis A should receive two doses of HAV vaccine 6 to 18 months apart. Laboratory tests should include tests for coinfection with HCV and/or HIV in those at risk.
Serum HBV DNA testing provides a direct measure of the level of viral replication. This quantification is essential for characterizing the status of infection, diagnosing the disease, making the decision to treat, and subsequent monitoring of patients. It is also important for predicting the risks of cirrhosis and HCC. Therefore, it should be applied to all patients diagnosed with CHB. The introduction of international unit (IU) (1IU is equivalent to five or six HBV DNA copies) as a recommended reporting unit for HBV DNA has facilitated the standardized reporting and comparison of serum HBV DNA levels.117
The methods used to quantify HBV DNA levels have evolved rapidly. Hybridization assays demonstrate reliable quantification of HBV DNA but are limited by their narrow range of detection (103
IU/mL). PCR-based assays have increased the sensitivity of HBV DNA detection to levels as low as 102
IU/mL. However, the quantification of many of the earlier PCR-based assays is not reliable at viral levels of >106
IU/mL. Real-time PCR-based assays have been introduced that demonstrate both high sensitivity and a broad linear range (10-108
IU/mL) of quantification.118
The same test should be specified each time when monitoring HBV DNA levels for a given patient in clinical practice in order to ensure consistency.
HBV genotype testing
HBV genotypes appear to influence the progression of disease, risk of HCC, and response to therapy.119
Some studies in Asia have suggested that genotype C is more frequently associated with HBV reactivation, severe liver disease, and HCC than is genotype B.119
The specific genotype has also been shown to affect the response to interferon therapy, with the rate of an antiviral response to pegylated interferon (peginterferon) therapy being higher for genotypes A and B than for genotypes C and D.125
In light of these data, foreign guidelines recommend performing genotyping selectively to help identify patients who might be at greater risk of disease progression, and routinely when wanting to determine the most appropriate candidates for peginterferon therapy.126
However, genotyping is recommended as being unnecessary in Korea because Korean patients are almost exclusively infected with genotype C.
Assessments of the severity of liver disease should include biochemical markers such as AST, ALT, gamma-glutamyl transpeptidase (GGT), alkaline phosphatase (ALP), prothrombin time (PT), and serum albumin. The ALT level is usually higher than AST levels, but the ratio may be reversed when the disease progresses to cirrhosis. A progressive decline in the serum albumin level and prolongation of the PT-often accompanied by a decrease in the platelet count-are characteristically observed after cirrhosis develops. The serum ALT level has been commonly used in assessments of liver disease and as an important criterion for defining which patients are candidates for the therapy.127
HBV-infected patients with normal or elevated ALT levels have been thought to have mild-to-no or significant necroinflammation on liver biopsy, respectively. However, there is no correlation between the degrees of liver cell necrosis and ALT level.128
ALT activity might also be affected by other factors such as body mass index, gender, abnormal lipid and carbohydrate metabolism, fatty liver, and uremia.128
Therefore, relying solely on the finding of elevated ALT as a prerequisite for treatment candidacy has limitations. Data from clinical studies have shown that the true normal level of ALT is significantly lower than the previously established limits: 40 IU/mL for men and 30 IU/mL for women. Moreover, data from cohort studies indicates that the upper limit of normal (ULN) ALT and AST levels should be decreased to 30 IU/mL for men and 19 IU/mL for women.128
Clinical studies have shown that patients with ALT levels of 20-45 IU/mL have a high risk of significant liver disease and mortality from complications.130
According to the treatment algorithm for CHB suggested by Keeffe et al., serum ALT levels of 30 and 19 IU/mL for men and women, respectively, should be used as the ULN levels when deciding to commence treatment.126
Further prospective studies are needed to clarify this issue.
A liver biopsy is recommended for determining the degree of necroinflammation and fibrosis in patients with elevated ALT, an HBV DNA level of >2,000 IU/mL, or both, because liver histology is very useful when deciding whether or not to commence treatment. However, its use is limited (and not mandatory) due to its invasiveness, it only sampling a small portion of the liver, and is low inter- and intraobserver reliabilities. Patients with high HBV DNA and normal ALT levels generally have less fibrosis in a liver biopsy and a poor response to antiviral therapy. Accordingly, this patient population is generally not considered for treatment. However, recent several clinical studies found that 12-43% of patients with persistent normal ALT levels had histologic evidence of significant fibrosis or inflammation in a biopsy, particularly among patients older than 35 years of age.125
A retrospective study of the relationship between ALT level and fibrosis in CHB patients produced similar results: of the 59 patients with persistent normal ALT levels, 18% had stage 2 fibrosis and 34% had grade 2 or 3 inflammation, with 37% of all patients with persistent normal ALT levels having significant fibrosis and inflammation.132
Subgroup analysis also demonstrated that most of the patients with fibrosis had high normal ALT levels. These results indicate that the ALT level in CHB patients with high normal ALT levels should be interpreted in conjunction with the level of serum HBV DNA, age, and liver histology results when deciding to commence treatment. Therefore, in HBsAg-positive patients with HBV DNA levels of ≥20,000 IU/mL and normal ALT levels, a liver biopsy should be considered in those older than 35 years since they are less likely to be in the immune-tolerance phase of infection. Treatment should be considered if a liver biopsy reveals fibrosis at stage 2 or greater and/or necroinflammation. When deciding whether to commence treatment in this patient population, it must be recognized that long-term therapy is likely to be needed due to the low probability of HBeAg seroconversion occurring within 1 year. A liver biopsy is also useful for evaluating other possible causes of liver disease such as nonalcoholic steatosis, steatohepatitis, or alcoholic liver disease. A liver biopsy is usually not required in patients with clinical evidence of cirrhosis or when treatment is indicated irrespective of the grade of activity or the stage of fibrosis. Although the efficacy of noninvasive methods such as using the Fibroscan device or measuring potential serum markers in assessing fibrosis in CHB has been studied in the past few years,126
such methods are not yet recommended as a diagnostic or decision-making tool for treatment.
Screening for hepatocellular carcinoma
The initial evaluation of patients with CHB should include tests to screen for HCC. Periodic surveillance is also needed in these patients to ensure the early detection of HCC during follow-up. The issue of HCC is treated in detail in the "Practical Guideline for Management of Hepatocellular Carcinoma 2009".133
Standard tools for HCC screening include measuring the α-fetoprotein level and ultrasound. Magnetic resonance imaging and computed tomography might be preferred for some patients with severe cirrhosis or obesity, since ultrasound has poor sensitivity in those conditions. Patients at a high risk of HCC include men older than 40 years, women older than 50 years, patients with cirrhosis, patients with a family history of HCC, and any carriers older than 40 years exhibiting persistent or intermittent ALT elevation, a high HBV DNA level (>2,000 IU/mL), or both.18
Keeffe et al. recently recommend earlier screening (at 30-35 years of age or even younger) in Asian patients with presumed infection at the time of birth or in early childhood due to the higher risk of HCC in these population.126
The initial evaluation of patients with CHB should include a thorough history-taking and physical examination, with emphasis on risk factors such as coinfection, alcohol consumption, and the family history of HBV infection and liver cancer (A1).
Laboratory tests to assess liver disease should include the complete blood count (CBC), AST/ALT, ALP, GGT, bilirubin, albumin, creatinine, and PT (A1).
Tests for HBV replication include HBeAg/anti-HBe and quantitative serum HBV DNA levels (A1). A real-time PCR quantification assay is strongly recommended for quantifying the HBV DNA level.
An anti-HCV test is necessary to rule out coinfection with HCV (B1).
An IgG anti-HAV test is necessary in CHB patients younger than 50 years (A1).
Standard tools for HCC screening include ultrasound and serum α-fetoprotein measurement (A1).
The goals of hepatitis B treatment are to decrease the mortality rate and increase the survival rate by alleviating hepatic inflammation and preventing the development of fibrosis, which ultimately decreases the progression of hepatitis to liver cirrhosis or HCC.134
The result of optimal treatment would be the loss or seroconversion of HBsAg, but since intranuclear cccDNA persists despite treatment, complete clearance of HBV is nearly impossible to achieve. This is why indices such as normalization of ALT level, undetectable HBV DNA, loss or seroconversion of HBeAg, and histologic improvement are used (rather than the loss or seroconversion of HBsAg) to predict the treatment response in the clinical context.
Elevation of the ALT level beyond the normal range indicates liver injury and the persistence of such elevation increaseses the risks of mortality and developing liver cirrhosis or HCC.130
The ALT level is a good predictor of the treatment response, and its normalization is used as a substitute index for predicting the treatment efficacy. However, the ALT level lacks specificity since it increases in liver diseases other than hepatitis B, and it might not increase even when viral replication is active in cases of immunologic tolerance or advanced liver disease. Therefore, the decision to treat cannot be made solely based on the ALT level.74
Biopsies can be useful for predicting treatment efficacy by confirming changes in the degree of hepatic inflammation and fibrosis between before and after treatment, but they are invasive and the assessment result can vary due to the sample size, sampling location, and interobserver variation.141
The HBV DNA level and HBeAg in CHB are indices of viral replication and active hepatitis, and patients with HBeAg-positive hepatitis B with high levels of HBV DNA have an increased risk of developing liver cirrhosis or HCC.74
The loss or seroconversion of HBeAg during the natural course of hepatitis B or after IFN-α treatment indicates a favorable long-term outcome with a decreased probability of liver cirrhosis or HCC development.29
Therefore, the clearance or seroconversion of HBeAg is an important goal of antiviral treatment in patients with HBeAg-positive active hepatitis. A decrease in the HBV DNA level has recently been suggested to be even more important.74
The decrease in the HBV DNA level after antiviral treatment in active hepatitis with elevated HBV DNA results in histologic improvement, seroconversion of HBeAg, and normalization of ALT levels, and thus a slowing of the progression of hepatitis.145
However, even in cases with HBV DNA levels of less than 104
cpm, which is considered to be inactive hepatitis, the hepatitis can still progress to liver cirrhosis and HCC.147
Therefore, a decrease in HBV DNA to an undetectable level is recommended for patients on antiviral treatment.
Many studies into the use of HBsAg as a substitute index for the treatment response are currently underway. In the natural course of hepatitis B, a loss of HBsAg occurs in 1-2% of patients annually, and the consequent decrease in the HBV DNA level results in decreases in the rates of disease progression to liver cirrhosis and HCC.29
The rate of HBsAg clearance was found to be high in cases of suppressed viral replication after IFN-α treatment149
and led to a decrease in liver disease-related mortality rates, such as loss of hepatic function and occurrence of HCC. Nonetheless, the rate of HBsAg clearance remains very low.149
The rate of HBsAg clearance was higher in the group treated with IFN than in the group treated with an oral antiviral agent.126
However, the prolonged use of oral antiviral agents is expected to increase the HBsAg clearance rate up to IFN levels.152
A positive correlation between the HBsAg titer and the HBV DNA level was also observed after entecavir and pegIFN treatment.153
Therefore, the clearance of HBsAg and its serum titer are together expected to be a good predictor of the hepatitis B treatment response in the future.
There are no clear guidelines regarding the optimal treatment period for oral antiviral agents after viral replication has been suppressed. HBeAg-negative hepatitis mostly recurs after ending treatment, despite the cessation criteria.155
In cases of HBeAg-positive hepatitis, the rate of persistent suppression of viral replication was higher when treatment was continued after seroconversion had been achieved.157
Many studies about the safety and efficacy of long-term oral antiviral treatment are currently underway.146
The treatment goals in hepatitis B are to decrease the mortality rate and increase the survival rate by alleviating hepatic inflammation and preventing the development of fibrosis, which would ultimately lower the progression of hepatitis to liver cirrhosis or HCC (A1).
To achieve HBsAg clearance, which is the ideal treatment goal, long-term maintenance of HBV DNA at an undetectable level is recommended (B1).
The ultimate treatment goals in patients with HBeAg-positive hepatitis are normalization of the ALT level, undetectable HBV DNA, and the clearance or seroconversion of HBsAg and HBeAg. In patients with HBeAg-negative hepatitis the treatment goals are normalization of the ALT level, undetectable HBV DNA, and the clearance or seroconversion of HBsAg (B1).
INDICATIONS FOR TREATMENT
Indications for initiating antiviral treatment
The ultimate goal of CHB therapy is to reduce mortality by preventing progression to hepatic decompensation and HCC. However, the study durations of currently available antiviral trials are not long enough to assess the effects of treatment on long-term survival.161
Long-term treatment with oral nucleoside or nucleotide analogues (NUCs) ameliorates histologic abnormalities such as necroinflammation and/or fibrosis, both in HBeAg-positive162
and HBeAg-negative 155
CHB. Therefore, long-term antiviral therapy may prevent disease progression and reduce the risk of liver cirrhosis.138
A recent meta-analysis indicated that long-term use of an oral antiviral agent decreased the risks of hepatic decompensation and HCC.167
Previous antiviral trials targeting HBV excluded patients in the immune-tolerant phase of the disease due to the minimal histologic changes they exhibit and the benign natural course of the disease.168
Criteria for initiating antiviral therapy for CHB
Elevated serum ALT is an indication for antiviral therapy37
because it reflects hepatic necroinflammatory activity and the risk of disease progression.171
The previously proposed cut-off value for transaminase (> 2× ULN) has recently been challenged: a prospective cohort study performed in Korea detected an association between increased liver-related mortality and transaminase levels of ≥ 20 IU/L.130
Moreover, ALT levels tend to decrease with age, especially in men.129
In healthy individuals without hepatitis virus infection or fatty liver, the 95th
percentile of the upper threshold of ALT is reported to be 30 IU/L for men and 19 IU/L for women.128
About two-thirds of CHB patients with mildly elevated ALT (1-2× ULN) show significant hepatic fibrosis (F2 or higher),173
and CHB patients with persistently normal ALT levels and HBV DNA levels of > 20,000 IU/mL may actually have significant fibrosis or inflammation,132
which are indications for antiviral therapy. A cohort study in Hong Kong demonstrated that the risk of liver-related complications in CHB patients was higher for ALT levels of 0.5-1× ULN and 1-2× ULN than for ALT levels of < 0.5× ULN.169
Thus, previous ALT criteria might exclude some patients with existing or potentially significant disease.175
Since advanced age is associated with significant hepatic fibrosis and poor outcomes in CHB,171
and defining the "inactive carrier state" according to ALT and HBV DNA levels may miss cases of histologically significant disease,174
histologic confirmation should be considered, especially in patients with advanced age when the serum AST/ALT levels are in the upper normal range or higher.
A serum HBV DNA level of ≥ 20,000 IU/mL has been suggested as a cut-off value for HBeAg-positive CHB.178
However, the distinction between HBeAg-negative CHB and inactive carriers is not clear due to the fluctuating course of HBeAg-negative CHB.178
A population-based cohort study revealed increased risks of liver cirrhosis and HCC when the serum HBV DNA level exceeds 2,000 IU/mL,74
and therefore this level is widely accepted as the cut-off for indicating antiviral therapy.
Antiviral therapy in liver cirrhosis
Patients with compensated cirrhosis and elevated serum HBV DNA can benefit from treatment with long-term oral NUCs, because such treatment may prevent disease progression134
and the development of HCC.137
There is increasing evidence of the beneficial role of oral nucleoside analogs in decompensated liver disease. Oral NUCs may improve hepatic function135
and decrease the need for liver transplantation in Child-Turcotte-Pugh class C cirrhosis.182
Patients in the immune-tolerant phase (HBeAg positive and persistently normal ALT level) are not indicated for antiviral therapy (B1).
HBeAg-positive CHB patients with an HBV DNA level of ≥ 20,000 IU/mL and an ALT level of ≥ 2× ULN are indicated for antiviral therapy (A1). When the ALT level is 1-2× ULN, a liver biopsy may be required to assess the need for antiviral treatment (B2). Antiviral therapy is indicated if a moderate-to-severe degree of inflammation or periportal fibrosis is present (A1).
HBeAg-negative CHB patients with an HBV DNA level of ≥ 2,000 IU/mL and an ALT level of ≥ 2× ULN are indicated for antiviral therapy (A1). When the ALT level is < 2× ULN, a liver biopsy may be required to assess the need for antiviral treatment (B2). Antiviral therapy is indicated if a moderate-to-severe degree of inflammation or periportal fibrosis is present (A1).
Patients with compensated cirrhosis are indicated for antiviral therapy if the HBV DNA level is ≥ 2,000 IU/mL, regardless of the ALT level (B1).
Patients with decompensated cirrhosis are indicated for antiviral therapy if HBV DNA is detectable, and liver transplantation should be considered (B1).
HBeAg positive and negative hepatitis
Indications for treatment
Long-term viral suppression by drugs with potent antiviral activity and high genetic barrier to resistance is a current paradigm of antiviral treatment for CHB aimed at the prevention of disease progression and improved survival. Since eradication of HBV infection is rarely achieved with currently available drugs, long-term treatment is necessary in most cases. Treatment protocol could be and should be individualized according to various factors: host factors such as mode of infection, disease status, and immunity; viral factors such as genotypes, prior antiviral treatment, mutation, and susceptibility level; and drug factors such local availability, cost, and reimbursement policy.37
CHB patients with active viral replication and significant inflammation and/or fibrosis are appropriate targets for antiviral treatment. Early guidelines generally agreed that antiviral treatment could be recommended for CHB patients (especially those without LC) with serum HBV DNA level > 20,000 IU/mL and serum ALT level> 2 × ULN.183
However, recent guidelines suggest that the indication of antiviral treatment should be expanded to those with lower serum HBV DNA levels and/or lower serum ALT levels.37
Serum HBV DNA level is a marker of viral replication and an indicator of efficacy of antiviral treatment in individuals with CHB. Progression to cirrhosis in HBV-infected patients is reported to be strongly correlated with the level of circulating virus.74
However, HBV DNA level of 105
cpm or 20,000 IU/mL was arbitrarily chosen by early guidelines as the cut-off level for indication of antiviral treatment. Some patients with lower serum HBV DNA levels (300-105
cpm), especially those with HBeAg negative hepatitis and/or cirrhosis, frequently show progression of liver disease and hence may need treatment.37
Serum ALT has been used as a convenient surrogate marker for liver injury, and elevated serum ALT was indicated as a risk factor for disease progression in CHB.76
Serum ALT level > 2 × ULN was suggested as a suitable indication of antiviral treatment for CHB by the early guidelines, especially in CHB patients without cirrhosis.183
However, an increased risk for developing LC and HCC has been documented in patients with mildly elevated serum ALT and even in those with serum ALT levels of upper normal range.128
Liver biopsy has three major roles: diagnosis, assessment of prognosis (disease staging), and assistance in making therapeutic decisions.186
In CHB, liver biopsy is especially useful for patients who do not meet definite criteria for treatment but still have a possible risk for significant disease.37
Age of the patient, serum HBV DNA level, serum ALT level, and family history of HCC should be considered before deciding whether or not to perform a biopsy.
Recommended antiviral agent as an initial therapy
Peginterferon-α and NUCs including lamivudine, adefovir, clevudine, telbivudine, entecavir, and tenofovir have been used for antiviral treatment of CHB. Drug of choice can differ according to various factors, including the effectiveness, safety, risk of resistance, and cost of drugs, preference of patients and doctors, and any plans for pregnancy.37
Peginterferon-α is preferred over conventional interferon due to its convenience of usage and high response rate. Lamivudine and telbivudine are not preferred due to their weak antiviral potency and high frequency of drug resistance, unless good response is predicted or anticipated duration of treatment is short. Adefovir is not an ideal option due to its weak antiviral activity and high frequency of drug resistance after 48 weeks. There are insufficient long-term follow-up data on efficacy and safety of clevudine. Entecavir and tenofovir are considerably safe agents showing potent viral suppression and low frequency of drug resistance. To date, there has been no report confirming the superiority of combination therapies over monotherapy in treatment-naïve patients.
Currently, monotherapy with entecavir, tenofovir, or peginterferon-α is the preferred initial therapy for CHB. Other NUCs might be used in patients with good predictors of response, and can be continued or modified according to on-treatment response. Elevated pretreatment ALT levels and/or active histologic disease were reported to be the most important predictors of lamivudine-induced HBeAg loss.127
During telbivudine treatment, a combination of pretreatment characteristics (HBV DNA< 109
cpm and ALT level ≥ 2 × ULN in HBeAg-positive patients; HBV DNA< 109
cpm in HBeAg-negative patients) plus non-detectable serum HBV DNA at treatment week 24 is suggested as the strongest predictor for optimal outcomes at 2 years.187
Of CHB patients receiving lamivudine or telbivudine treatment, those with virologic response at week 24 (< 300 cpm) were indicated to achieve high rate of HBeAg seroconversion at week 52.132
Less resistance was reported in patients showing lower serum HBV DNA level (< 1,000 cpm) at week 48 during long-term therapy with adefovir.165
Antiviral therapy is not indicated for patients in immune tolerance phase. Spontaneous HBeAg seroconversion might be anticipated in some patients with HBeAg positive hepatitis. Serum level of AST or ALT could stabilize after transient elevation without specific treatment. Long-term treatment is necessary in a large proportion of patients receiving NUC therapy, which is associated with problems of high cost and emergence of drug resistance. Hence, careful consideration is necessary for deciding whom, when, and how to treat.
HBeAg positive chronic hepatitis B
HBeAg positive CHB patients with HBV DNA>20,000 IU/mL, and serum AST or ALT> 2 × ULN or significant inflammation or fibrosis (≥ moderate necroinflammation; ≥ periportal fibrosis) on biopsy should be considered for treatment (A1). Treatment can be delayed for 3-6 months if spontaneous HBeAg seroconversion is anticipated (B2). However, patients with apparent or concerned liver failure (i.e., those with jaundice, prolonged PT, hepatic encephalopathy, and ascites) should be promptly treated (B1).
For those with HBV DNA>20,000 IU/mL and serum AST or ALT = 1-2 × ULN, observation or liver biopsy can be considered. Antiviral treatment is recommended for those showing subsequent elevation of serum ALT or AST, or significant inflammation or fibrosis on biopsy (A1).
Monotherapy with entecavir, tenofovir, or peginterferon-α is preferred (A1). Other NUCs might be used in patients with good predictors of response, and can be sustained or modified according to on-treatment response (B2).
HBeAg negative chronic hepatitis B
HBeAg negative CHB patients with HBV DNA>2,000 IU/mL and serum AST or ALT> 2 × ULN or significant inflammation or fibrosis on biopsy should be considered for treatment (A1).
For those with HBV DNA> 2,000 IU/mL and serum AST or ALT< 2 × ULN, observation or liver biopsy can be considered. Antiviral treatment is recommended for those showing subsequent elevation of serum ALT or AST, or significant inflammation or fibrosis on biopsy (A1).
Monotherapy with entecavir, tenofovir, or peginterferon-α is preferred (A1). Other NUCs might be used in patients with good predictors of response, and can be sustained or modified according to on-treatment response (B2).
Compensated liver cirrhosis
The suppression of viral replication by long-term antiviral therapy may improve hepatic inflammation and fibrosis, which would stop the disease progressing to decompensated liver cirrhosis and HCC134
Antiviral therapy is recommended in patients with CHB in whom significant hepatic fibrosis exists regardless of the AST/ALT levels.37
The levels of AST/ALT should not be used as criteria for starting antiviral therapy in patients with liver cirrhosis, because they already have significant hepatic fibrosis and frequently have nearly normal AST/ALT levels.
In a cohort of HBeAg-positive liver cirrhosis patients, long-term follow-up data after interferon-α therapy showed that the HBeAg seroconversion rate was similar (67% vs. 60%, respectively) but that the ALT normalization rate (62% vs. 47%) and HBsAg loss rate (23% vs. 3%) were better in the interferon-α-treated group than in the control group.190
Interferon-α treatment in cirrhotic patients requires careful monitoring because it may cause acute exacerbation of hepatitis that leads to hepatic failure.191
After treating CHB patients with peginterferon-α-2b alone or in combination with lamivudine for 52 weeks, the virologic response rate (as indicated by HBeAg seroconversion and an HBV DNA level of <10,000 cpm) was superior in those with cirrhosis than in those without cirrhosis (35% vs. 14%, respectively).192
However, acute exacerbation of hepatitis (33% vs. 12%, respectively) and requirement of dose reduction (63% vs. 30%) were more common in cirrhotic patients than in noncirrhotic patients.192
Therefore interferon-α may be used with caution in cirrhotic patients with preserved liver function. Therefore interferon-α may be used with caution in cirrhotic patients with preserved liver function.134
Entecavir treatment of patients with advanced hepatic fibrosis or cirrhosis for 48 weeks produced improvements in the liver histology in 57%, 59%, and 43% of patients with HBeAg-positive, HBeAg-negative, and lamivudine-resistant CHB, respectively.193
A study including a small number (n=40) of patients showed that telbivudine effectively decreased HBV DNA levels in patients with compensated liver cirrhosis, and the undetectablity of HBV DNA after 48 weeks of telbivudine treatment was 92.5%.194
A study comparing the effects of clevudine treatment for 48 weeks found that the virologic response rate (HBV DNA <1,000) (87.1% vs. 71.4%, respectively) and biochemical response rate (83.9% vs. 80.9%) did not differ significantly between patients with CHB (n=21) and those with liver cirrhosis (n=31).195
Phase-3 clinical trials of adefovir and tenofovir have included some patients with liver cirrhosis, but there has been no report on the effects of these drugs in patients with compensated liver cirrhosis.
Long-term antiviral therapy is generally required in patients with liver cirrhosis, which has led to AASLD and EASL guidelines recommending the use of entecavir or tenofovir due to their potent antiviral efficacy and high genetic barrier to drug resistance. AASLD and EASL guidelines recommend combinational use of adefovir or tenofovir to prevent the development of drug-resistant viruses in circumstances when low-genetic-barrier drugs such as lamivudine or telbivudine are selected as an initial therapy. However, there appears to be only weak evidence for supporting this approach.37
Meanwhile, the APASL guideline published in 2008 recommends the use of interferon/peginterferon, entecavir, adefovir, telbivudine, or lamivudine in patients with CHB, and it seems likely that these recommendations are influenced by considerations of socioeconomic status in Asian countries.170
In general, long-term antiviral therapy is required in patients with liver cirrhosis, therefore close monitoring about the possible development of drug resistance and acute flare of hepatitis, and it is necessary to differentiate the emergence of drug resistance and poor drug compliance when decompensation develops during treatment.
Antiviral therapy is recommended in patients with compensated liver cirrhosis if the HBV DNA level is ≥2,000 IU/mL regardless of the AST/ALT levels (B1).
Oral antiviral therapy using nucleoside/nucleotide analogues is recommended in patients with compensated liver cirrhosis. Long-term treatment is generally required, and hence the choice of drug is based on the general principles of hepatitis B treatment with consideration of antiviral efficacy, side effects, and genetic barriers to drug-resistant viruses (B1).
Peginterferon-α may be used with careful monitoring for the imparement of liver function and drug side effects in patients with compensated liver cirrhosis having preserved liver function (B2).
Decompensated liver cirrhosis
It is preferable for patients with decompensated liver cirrhosis to be treated at an institution that can provide appropriate management for cirrhosis complications. Liver transplantation should be considered in patients with decompensated liver cirrhosis. The use of interferon-a in patients with decompensated liver cirrhosis is contraindicated due to the possibility of serious complications such as infection or hepatic failure.196
Lamivudine treatment for longer than 6 months was shown to improve or stabilize liver function and prolong the time to liver transplantation in patients with decompensated liver cirrhosis.197
A study comparing the effects of telbivudine with lamivudine in patients with decompensated liver cirrhosis found that the higher HBV DNA undetectability (47% vs. 36%, respectively) and the lower viral breakthrough rate (29% vs. 39%, respectivelyy) in the telbivudine group than in the lamivudine group.200
A study investigating the effect of adefovir in lamivudine-resistant cirrhotic patients (n=101) found that the virologic response rate was lower in decompensated cirrhotic patients (n=53) than in compensated cirrhotic patients (n=48) (50.9% vs. 83.3%, respectively), whereas ALT normalization and HBeAg loss did not differ between the two groups.201
A randomized study comparing the effects of entecavir (1 mg/day) and adefovir (10 mg/day) in patients with decompensated liver cirrhosis found that the rates of HBV DNA undetectability at weeks 24 and 48 were higher in the entecavir group than in the adefovir group (week 24, 49% vs. 16%, respectively; week 48, 57% vs. 20%), while HBeAg seroconversion at week 48 did not differ significantly between the two groups (6% vs. 10%).202
Entecavir therapy improved the Child-Pugh score (to ≥2) in almost half (27/55) of treatment-naive patients with decompensated liver cirrhosis (n=55), and the 1-year transplantation-free survival rate was 87.1%.135
A randomized trial comparing the effects of tenofovir (n=45), tenofovir plus emtricitabine (n=45), and entecavir (n=22) in patients with decompensated liver cirrhosis showed that the requirement of early withdrawal of drug (6.7%, 4.4%, and 9.1%, respectively) and the elevation of serum creatinine (8.9%, 6.7%, and 4.5%) did not differ between the three groups. The rates of undetectable HBV DNA at week 48 were 70.5%, 87.8%, and 72.7%, respectively, and those of HBeAg loss/seroconversion were 21%/21%, 27%/13%, and 0%/0%.136
Because prompt treatment is required in patients with decompensated liver cirrhosis, oral antiviral therapy is the treatment of choice if HBV DNA is detectable in PCR tests.37
The recommended antiviral drug has a potent antiviral efficacy and high genetic barrier to drug resistance. The clinical improvement often requires 3-6 months of antiviral therapy, which can result in some patients progressing to hepatic failure even during antiviral therapy, and hence liver transplantation needs to be considered.199
Pre- and post-transplantation antiviral therapy may reduce the risk of reactivation of hepatitis after liver transplantation.
Prompt antiviral therapy is recommended in patients with decompensated liver cirrhosis if HBV DNA is detectable in PCR tests regardless of the AST/ALT levels (B1).
The treatment of choice in patients with decompensated liver cirrhosis is oral nucleoside or nucleotide analogues that have potent antiviral efficacies and high genetic barriers to drug resistance (B1); however, long-term data about the efficacy and safety of these drugs are not available yet.
The use of interferon/peginterferon is contraindicated in patients with decompensated liver cirrhosis due to the possibility of serious complications such as infection or hepatic failure (A1).
Liver transplantation should be considered in patients with decompensated liver cirrhosis (B1).
Combination therapy in treatment naïve patients
It has been shown that combination antiviral therapy is more effective than monotherapy in the treatment of patients with HCV or HIV infection. The potential benefits from combination therapy are additive or synergistic antiviral efficacy and reduction or delay of the occurrence of resistant viruses. Meanwhile, the possible limitations of this approach are increased toxicity and cost, drug interactions, and poor compliance. Studies investigating the effects of combination therapy of interferon/peginterferon plus lamivudine found no benefit relative to interferon/peginterferon monotherapy.203
Similarly, combination therapy of interferon-α plus lamivudine was not more effective than lamivudine monotherapy in nonresponders to interferon.208
A study found that combination therapy of peginterferon plus adefovir for 48 weeks showed higher HBeAg seroconversion (58%) and HBsAg seroconversion (15%); however, this study had limitation of the small number of patients and the absence of a control group.209
There have been no reports on the efficacy of combination therapy of peginterferon-a plus recently developed potent oral antiviral agents.
Few reports have compared the effects of combination therapy and monotherapy in treatment-naïve patients with CHB. Combination therapy has not demonstrated better efficacy than monotherapy. Combination therapy of lamivudine plus adefovir and lamivudine monotherapy showed similar antiviral effects. Fewer lamivudine-resistant viruses developed in the combination group than in the monotherapy group (15% vs. 43%, respectively), however combination therapy could not completely prevent the development of resistant virus.210
Another study found that combination therapy of lamivudine plus telbivudine provided no benefit relative to telbivudine monotherapy.211
A small-sample study found that combination therapy of adefovir plus emtricitabine provided better viral suppression than adefovir monotherapy, but there was no difference in the HBeAg seroconversion rate.212
The patients most likely to benefit from combination therapy as the first-line antiviral treatment would be those with a high risk of developing resistant viruses (due to long-term infection, very high pretreatment HBV DNA titer, and the presence of mutant HBV prior to treatment) and in whom the emergence of resistant viruses can be life-threatening (e.g., cirrhotic and post-transplant patients).213
AASLD and EASL guidelines recommend the combination therapy of adefovir or tenofovir to prevent the development of drug resistant virus in circumstances when low genetic barrier drugs such as lamivudine or telvbivudine are need to be selected as an initial therapeutic agent.37
There is no evidence that combination therapy including low-genetic-barrier drugs is better than monotherapy at decreasing the development of resistant viruses. Moreover, there are no long-term safety data on the combination therapy of entecavir plus tenofovir, and the cost issue also needs to be addressed. Likewise, the effects of combining tenofovir with lamivudine, telbivudine, or emtricitabine require further investigation.
Combination antiviral therapy in treatment-naïve patients is not recommended since there are no data supporting the superiority of combination therapy over monotherapy (B1).
Monitoring prior to antiviral treatment
After diagnosis and the initial evaluation of patients with CHB, their serum HBV DNA, ALT, HBeAg, and anti-HBe levels should be regularly monitored until they are considered for treatment.37
The HBV genotype test is not recommended in Korea because most Korean patients are known to have HBV genotype C.216
Several studies reported that applying a quantitative HBsAg assay before or during antiviral treatment may help in predicting the treatment response.218
Chronic hepatitis (with HBeAg positivity or negativity)
A. In patients with persistently normal AST/ALT levels, liver function should be tested and serum HBV DNA should be measured by real-time PCR at 2-6 month intervals, and HBeAg status (HBeAg and anti-HBe) should be checked every 6-12 months (III, C1).
B. If AST/ALT levels increase above the normal limit, liver function should be tested every 1-3 months, and serum HBV DNA should be measured by real-time PCR and HBeAg status checked every 2-6 months (III, C1).
Compensated liver cirrhosis
-Liver function should be tested every 2-6 months, and serum HBV DNA should be measured by real-time PCR and HBeAg status checked every 2-6 months (III, C1).
Decompensated liver cirrhosis
-Liver function should be tested every 1-3 months, and serum HBV DNA should be measured by real-time PCR and HBeAg status checked every 2-6 months (III, C1).
Monitoring during antiviral treatment
Patients receiving peginterferon-α should be tested monthly for serum CBC and ALT level. Serum HBV DNA should be measured after 3-6 months of treatment to verify the primary response. All patients treated with peginterferon-α should be checked for the known adverse effects of interferon at every visit.
HBeAg-positive chronic hepatitis
Patients should be tested for HBeAg and anti-HBe at 6 and 12 months during the treatment, and at 6 months post treatment. After cessation of treatment, patients should be monitored for 6-12 months to check if additional treatment is required. The optimal treatment outcome is HBeAg seroconversion, ALT normalization, and serum HBV DNA of less than 2,000 IU/mL. There is high probability of HBsAg loss if serum HBV DNA becomes undetectable during treatment. HBeAg-positive patients who achieve HBeAg seroconversion with peginterferon-α require a long follow-up due to the possibility of HBeAg reversion or development of HBeAg-negative CHB. HBsAg loss should be checked at 6-month intervals after HBeAg seroconversion if serum HBV DNA is undetectable. Several studies reported that the quantitative HBsAg assay may help in predicting the treatment response. In case of a primary non-response (failure to achieve a 1 log10 reduction of serum HBV DNA from baseline after 3 months of peginterferon-α treatment), peginterferon-α treatment should be stopped and replaced by a nucleos(t)ide analogue (NUC).
HBeAg-negative chronic hepatitis
HBeAg-negative patients should be monitored similarly to HBeAg-positive patients during 48 weeks of treatment. A virologic response with serum HBV DNA of <2,000 IU/mL is generally associated with remission of the liver disease. Undetectable serum HBV DNA by real-time PCR is the ideal off-treatment sustained response, with a high probability of HBsAg loss in the longer term. HBsAg should be checked at 6-month intervals if HBV DNA is not detectable.
In a compliant patient with a primary non-response (decrease in serum HBV DNA of <2 log10 IU/mL after 6 months or more of NUC treatment), changing to or adding a more-potent drug should be considered. Serum HBV DNA should be measured every 1 to 3 months for the first months to ascertain the virologic response, and then every 3 to 6 months. Serum HBV DNA reduction to an undetectable level by real-time PCR (i.e.,<10-15 IU/mL) should ideally be achieved to avoid resistance. Serum HBV DNA monitoring is thus critical to detecting treatment failure.
Compliance and antiviral-resistance mutation should be monitored in patients who develop virologic breakthrough while receiving NUC, and appropriate rescue therapy should be initiated if necessary.220
Most NUCs are excreted through the kidney, and hence dose adjustment is required in patients with renal insufficiency (Table 6
and regular monitoring of renal function should be performed in patients receiving adefovir or tenofovir. Moreover, there are several reports associating tenofovir with bone loss in patients with HIV, and studies of entecavir-related carcinogenicity are in progress. There have been few reports on telbivudine-related myositis. Combination therapy of peginterferon-α plus telbivudine is not recommended due to the possibility of inducing peripheral neuritis.
During NUC therapy, liver function should be tested and serum HBV DNA should be measured by real-time PCR every 1-3 months, and HBeAg status (HBeAg and anti-HBeAg) should be checked every 3-6 months (III, C1).
During peginterferon therapy, CBC and ALT level should be measured monthly. Serum HBV DNA should be measured by real-time PCR at 1-to 3-month intervals, and HBeAg and anti-HBe should be checked at 6 and 12 months during the treatment and at 6 months post treatment (III, C1).
After verifying a complete virologic response, serum HBV DNA should be measured by real-time PCR at 3-6 months and then retesting should be performed at 2-3 months after HBeAg seroclearance is achieved (III, C1).
Patients who develop virologic breakthrough while receiving NUC should be monitored for compliance and antiviral-resistance mutation (A1).
During antiviral therapy, a close monitoring for side effects of each drug is mandatory (I, A1).
Monitoring after antiviral treatment
The response to antiviral treatment persists in some patients while relapsing in others. Non-responders also should prepare for the deterioration of liver function. Therefore, regular monitoring is needed to check for the durability of the treatment response, relapse, and liver function.
During the first year after antiviral treatment, liver function should be monitored and serum HBV DNA should be measured by real-time PCR every 1-3 months, and HBeAg and anti-HBe should be checked at 3-to 6-month intervals. Beyond 1 year after antiviral treatment, liver function and serum HBV DNA by real-time PCR should be tested every 3-6 months to detect viral relapse (III, C1).
For early detection of HCC, ultrasound and serum a-fetoprotein measurement should be performed regularly (III, A1).
CESSATION OF TREATMENT
HBeAg-positive chronic hepatitis
The primary endpoint when treating patients with HBeAg-positive hepatitis is to achieve HBeAg seroconversion. Undetectable serum HBV DNA by real-time PCR and HBeAg seroconversion are strongly correlated with favorable biochemical and histologic responses. Peginterferon-α is generally administered for 48 weeks, and its efficacy was confirmed in a recent double-blind, randomized controlled study.225
NUC can be stopped when HBeAg seroconversion is achieved and antiviral treatment has maintained at least for 12 months.158
HBsAg should be tested at 6-month intervals after HBeAg seroconversion; however, HBsAg loss is rarely observed after NUC therapy.
HBeAg-negative chronic hepatitis
The recommended duration of peginterferon-α treatment in patients with HBeAg-negative hepatitis is 48 weeks, but the optimal treatment duration for NUC is not known, and cessation of treatment should be individually decided according to the clinical treatment response and the baseline severity of the liver disease. Treatment with NUC should be continued until the loss of HBsAg. However, treatment discontinuation can be considered if undetectable serum HBV DNA has been documented on three separate occasions 6 months apart.170
Long-term treatment is required in patients with cirrhosis. In HBeAg-positive patients with compensated cirrhosis, treatment discontinuation can be considered when NUC is administered for at least an additional 12 months after HBeAg seroconversion. Treatment discontinuation can be considered after HBsAg loss is achieved in HBeAg-negative patients. Monitoring for viral relapse and acute exacerbation of disease is mandatory after discontinuation. Long-term treatment should be planned in patients with decompensated cirrhosis, including the possibility of liver transplantation.
HBeAg-positive chronic hepatitis
1) Peginterferon should be administered for 48 weeks (A1).
2) NUC should be administered at least 12 months after serum HBV DNA is undetectable and HBeAg seroclearance or seroconversion is attained (II-2, B1).
HBeAg-negative chronic hepatitis
1) Peginterferon-α should be administered for at least 48 weeks (B1).
2) It is not clear how long NUC should be continued, but this should be at least until HBsAg loss (A1).
Patients with cirrhosis need long-term treatment (II, B1).
DEFINITIONS OF RESPONSE AND PREDICTORS OF RESPONSE
Definitions of treatment responses (Table 7)
The definitions of responses to antiviral therapy vary with the type of therapy.
A primary non-response to peginterferon-α is defined as a decrease of less than 1 log10 IU/mL in serum HBV DNA from baseline after 3 months of therapy. A virologic response is defined as an HBV DNA level of less than 2,000 IU/mL after 6 months of therapy. A serologic response is defined by HBeAg seroconversion in patients with HBeAg-positive CHB.
A primary non-response
to NUC is defined as a decrease of less than 2 log10
IU/mL in serum HBV DNA from baseline after 6 months of therapy. A complete virologic response
is defined as undetectable serum HBV DNA by real-time PCR. A partial virologic response
is defined as a decrease in serum HBV DNA of more than 1 log10
IU/mL but with serum HBV DNA still being detectable by real-time PCR.227
Partial virologic response should be assessed to determine whether to modify the current therapy after 24 weeks of treatment for moderately potent drugs or drugs with a low genetic barrier to resistance (lamivudine and telbivudine), and after 48 weeks of treatment for highly potent drugs, drugs with a high genetic barrier to resistance, and drugs with a late emergence of resistance (e.g., entecavir, adefovir, and tenofovir). Virologic breakthrough
is defined as a confirmed increase in serum HBV DNA of more than 1 log10
IU/mL relative to the nadir serum HBV DNA during therapy. This usually precedes a biochemical breakthrough
, which is characterized by an increase in ALT level after an initial normalization. If a virologic breakthrough develops in a compliant patient, antiviral-resistant mutations should be tested for. Genotypic resistance
is defined as the presence of HBV mutations from a patient's serum that confers resistance to the antiviral agent, and phenotypic resistance
is defined as the presence of decreased susceptibility of HBV mutations to antiviral drugs in an in vitro
is where HBV mutation induced by one antiviral agent confers resistance to other antiviral agents.
HBV resistance to NUCs is characterized by the presence of HBV variants with amino-acid substitutions that confer reduced susceptibility to the administered NUC. Such resistance may result in primary treatment failure or virologic breakthrough during therapy.
Predictors of treatment responses
Certain baseline and on-treatment predictors of the subsequent treatment response have been identified. The predictors of the responses for existing antiviral therapies at various time points vary with the agent.
Pretreatment factors predictive of HBeAg seroconversion in HBeAg-positive patients are a high ALT level, low viral load, a high inflammatory activity score in a liver biopsy, and HBV genotypes.204
There is no consensus among previous reports for patients with HBeAg-negative hepatitis, but generally a pretreatment high ALT level, young age, and female gender are reported to be associated with a favorable treatment response.131
A decrease in serum HBV DNA to less than 20,000 IU/mL after 12 weeks of treatment is associated with a 50% chance of HBeAg seroconversion in HBeAg-positive patients and with a 50% chance of a sustained response in HBeAg-negative patients.131
A decrease in HBeAg at week 24 may predict HBeAg seroconversion.127
Further studies are needed to determine the usefulness of HBsAg quantification in predicting a sustained virologic response and HBsAg loss.218
HBV genotypes A and B have been shown to be associated with a better response to interferon-α than genotype C, in terms of HBeAg seroconversion and HBsAg loss.203
However, knowledge of the HBV genotype has a poor predictive value in individual cases, and currently genotype alone should not dominate the choice of treatment.
Pretreatment factors predictive of HBeAg seroconversion are a low viral load (serum HBV DNA of <107
IU/mL), high ALT level (<3×ULN), and high inflammatory activity score in a liver biopsy (at least A2).234
A high pretreatment ALT level is known to be the most important predictor of the treatment outcome for lamivudine, adefovir, or telbivudine.127
During treatment with lamivudine, adefovir, or telbivudine, a virologic response at 24 or 48 weeks (undetectable serum HBV DNA by a real-time PCR assay) is associated with lower incidences of antiviral resistance (i.e., higher probability of a sustained virologic response) and HBeAg seroconversion in HBeAg-positive patients.165
HBV genotype does not influence the response to any NUC.
The development of antiviral resistance is one of the most important factors predicting the success or failure of CHB treatment. The emergence of antiviral resistance results in the resumption of active viral replication that had been suppressed after the initiation of antiviral therapy, and can impair the biochemical or histologic improvement.237
Therefore, the prevention, early diagnosis, and management of antiviral resistance may significantly affect the long-term prognosis in CHB patients receiving antiviral therapy.134
Mechanism of antiviral resistance and definitions
It is estimated that more than 1011
new virions are produced every day in a human body with active HBV replication.238
Some of the HBV mutants that emerge naturally during active replication are selected under specific selection pressures exerted by the human immune system or antiviral therapy. Those mutants with maximal replication become predominant during antiviral therapy. The replication fitness is determined by the replication capacity and the fold resistance (i.e., quantified as the drug concentration needed to suppress 50% of mutant virus replication or to suppress 50% of wild-type virus replication) of the mutant viruses. Primary antiviral-resistant mutants usually have a low replication capacity, but recover to the level of the wild-type virus when compensatory mutations appear.239
In addition, a higher fold resistance to antiviral therapy allows increased replication of the mutant virus. A genetic barrier is defined as the number of genetic mutations needed to develop antiviral resistance, with a higher genetic barrier indicating a lower risk of resistance.240
The antiviral potency of drugs also influences the development of resistance. Drugs with a lower antiviral potency or potent antiviral activity have lower risks of antiviral resistance, because the former is associated with a lower selection pressure and the latter with complete suppression of the virus. However, drugs with intermediate potency have an increased risk of resistance because residual viremia during treatment may result in selection of mutants with good replication fitness.241
Clinically, the HBV DNA level, history of prior antiviral treatment, duration of treatment, serum drug concentration (peak and trough), and patient compliance are the most important factors influencing the development of resistance. Definitions associated with antiviral resistance are listed in Table 7
Mutations conferring resistance to antiviral agents
Antiviral agents for the treatment of HBV infection are classified into two groups: nucleoside analogues and nucleotide analogues. Cyclopentenes (entecavir) and L-nucleoside analogues (lamivudine, telbivudine, and clevudine) are nucleoside analogues, while acyclic phosphonates (adefovir and tenofovir) are nucleotide analogues.242
The incidences of resistance to individual antiviral drugs are summarized in Table 8
1. Nucleoside analogues
1) L-nucleoside analogues (lamivudine, telbivudine, and clevudine)
Mutations at rtM204 are considered the primary resistance mutations to lamivudine, telbivudine, and clevudine.243
The rtM204V and rtM204I mutations involve the substitution of methionine with valine and isoleucine, respectively, at codon 204 of the reverse transcriptase gene. Originally these were called YMDD mutations, but that terminology is no longer recommended.247
rtM204V emerges during lamivudine treatment, but rtM204I can develop during the administration of lamivudine, telbivudine, or clevudine.235
An rtM204V mutant may commonly accompany rtL180M but not rtM204I.251
These mutants are sensitive to adefovir and tenofovir, but they exhibit cross-resistance to entecavir and show an eightfold decrease in sensitivity. The rtA181T mutation has been detected in 5% of lamivudine-resistant patients.252
The mutants exhibit cross-resistance to adefovir but remain sensitive to entecavir.252
2) Cyclopentene (entecavir)
Resistance to entecavir develops via a two-hit mechanism. rtL180M and rtM204V first develop as background mutations, and then additional mutations such as rtT184L/F/A/M/S/I/C/G, rtS202G/I/C, or rtM250V/I/L develop as primary resistance mutations to entecavir, resulting in a remarkable decrease in drug susceptibility.240
rtI169T is a compensatory mutation that increases the fold resistance of rtT184, rtS202, and rtM250 mutants. Since multiple genetic mutations are needed to develop high-level resistance to entecavir (high genetic barrier), the resistance rate in treatment-naïve subjects is very low. However, a resistance rate as high as 51% has been reported after 5 years of treatment in lamivudine-refractory subjects.254
2. Nucleotide analogues
rtN236T and rtA181V/T are the primary resistance mutations to adefovir.165
The fold resistances of rtN236T and rtA181T to adefovir are 7- to 10-fold and 2.5- to 5-fold, respectively, compared to the wild-type virus.242
rtA181T can be detected in subjects receiving lamivudine monotherapy or a combination therapy of adefovir plus lamivudine.256
Clinically significant resistance mutations to tenofovir have not been reported in patients with HBV monoinfection. However, rtA194T can decrease the susceptibility to tenofovir by 10-fold in the presence of rtL180M+rtM204V, according to a case study of a patient with HBV and HIV coinfection.258
Management of antiviral resistance: general principles
Prior antiviral resistance predisposes individuals to subsequent viral mutations and limits the choice of rescue therapies due to the presence of cross-resistance (Table 9
Even though antiviral agents without cross-resistance may be selected, the resistance to the rescue therapy is greater than that of treatment-naïve subjects.259
It is therefore critical to initially choose the antiviral agent with the lowest resistance rate (Table 10
Appropriate monitoring is needed during treatment in order to detect virologic and biochemical breakthroughs as early as possible. Antiviral resistance testing is needed when a virologic or biochemical breakthrough is detected in subjects with good compliance. If genotypic resistance is confirmed, rescue therapy should be initiated before the clinical manifestation deteriorates,262
and the regimen should include a drug without cross-resistance to a prior antiviral agent. Nucleotide analogues must be combined to manage resistance to nucleoside analogues, while nucleoside analogues must be combined to manage resistance to nucleotide analogues. The combination of antiviral agents from two different groups of nucleos(t)ide analogues is expected to decrease the risk of antiviral resistance and is especially recommended in patients who need long-term antiviral therapy, those with a high viral load, and those with decompensated liver function.
General principles of antiviral resistance management:
An antiviral resistance test should be performed when virologic breakthrough occurs although compliance is good (A1).
Rescue antiviral therapy should be started for antiviral resistance as soon as possible, especially when viral breakthrough is detected and genotypic resistance is confirmed (A1).
Sequential monotherapy should be avoided in order to prevent multidrug resistance. Combinations of nucleoside analogues (lamivudine, telbivudine, clevudine, or entecavir) and nucleotide analogues (adefovir or tenofovir) without cross-resistance are strongly recommended (A1).
Management of antiviral-resistant CHB: individual antiviral agents
1. Management of lamivudine resistance
The drugs listed below have been found to be effective at suppressing replication in lamivudine-resistant HBV.
A pilot study that compared the efficacy of adefovir monotherapy with combination therapy of lamivudine plus adefovir against lamivudine-resistant HBV infection found comparable reductions of viral load (-4.4 vs. -3.59 log10
cpm, respectively) and normalizations of the ALT level (53% vs. 47%). However, a transient ALT flare was found in 37% of the patients in the adefovir-monotherapy group.263
Therefore, switching to adefovir monotherapy or a short term (2-3 months) combination of adefovir and lamivudine at the beginning of adefovir rescue therapy to prevent ALT flare was considered. However, subsequent studies found that adefovir resistance emerged in patients with lamivudine resistance who were switched to adefovir monotherapy (in 18% of patients at 1 year, 25% at 2 years,260
and up to 65% after 5 years221
), suggesting adefovir monotherapy for lamivudine-resistant HBV infections has limited efficacy. On the other hand, when lamivudine-resistant HBeAg-negative CHB patients were followed up for approximately 3 years in a small prospective study, the development of resistance to adefovir was significantly less common in the adefovir-plus-lamivudine combination-therapy group than in the adefovir-monotherapy group (0% and 21%, respectively).264
In a subsequent larger, population-based study in Italy that enrolled 588 HBeAg-negative CHB patients, the rate of virologic breakthrough (2% and 9%, respectively) and rate of adefovir resistance development (0.8% and 5%) were significantly lower in the adefovir-plus-lamivudine combination-therapy group than in the adefovir-monotherapy group, supporting the efficacy of combination therapy.265
However, lamivudine-resistant strains (e.g., rtA181T) can continuously be detected even after combination therapy of adefovir plus lamivudine, so caution is necessary to avoid the possibility of multidrug-resistant HBV.256
Other options for lamivudine resistance include adding one of the nucleoside analogues (entecavir, clevudine, or telbivudine) to adefovir.267
Future studies should compare the efficacies of these regimens with that of the adefovir-plus-lamivudine combination therapy.
Tenofovir has shown potent antiviral activity against lamivudine-resistant HBV as well as wild-type HBV.271
One retrospective study involving 53 lamivudine-resistant CHB patients found that the HBV DNA level after 48 weeks was less than 105
cpm in 100% of patients in the tenofovir group but in only 44% of patients in the adefovir group, with the difference being statistically significant.271
The mean change in the HBV DNA level was greater in the tenofovir group (-5.5 log10
cpm) than in the adefovir group (-2.8 log10
The stronger antiviral effect of tenofovir might be due to the dose differing between the two drugs (300 mg of tenofovir vs. 10 mg of adefovir). Another retrospective study administered tenofovir to 20 patients who showed persistent HBV replication (>104
cpm) despite receiving adefovir treatment for longer than 15 months. HBV DNA was not detected in 95% of the patients after 3.5 months of tenofovir treatment (in a PCR assay with a lower detection limit of 400 cpm).272
In a recent study with a longer follow-up period of up to 23 months, tenofovir monotherapy resulted in 100% DNA undetectability (in PCR assay) among lamivudine-resistant CHB patients.273
Therefore, treatment strategies that include tenofovir seem to be more effective than those involving adefovir in overcoming lamivudine resistance. However, there is a report of tenofovir resistance in a lamivudine-resistant CHB patient who received tenofovir monotherapy, so the efficacy of tenofovir monotherapy requires further evaluation.258
In this context, one recent study found that the reduction in the HBV DNA level among 109 lamivudine-resistant CHB patients was greater in the tenofovir-plus-lamivudine combination-therapy group (-5.3±1.8 log10
cpm, mean±SD) than in the tenofovir-monotherapy group (-4.7±1.5 log10
cpm), adefovir-monotherapy group (-2.4±2.5 log10
cpm), and adefovir-plus-lamivudine combination-therapy group (-2.2±1.6 log10
More recently, combination therapy of tenofovir plus telbivudine produced a higher rate of virologic response (defined as a reduction of more than 2 log10
cpm in the HBV DNA level) than combination therapy of tenofovir plus lamivudine (64% vs. 45%, respectively) after 12 months of treatment.275
Entecavir exhibits some cross-resistance with lamivudine, which prompted a dose of 1.0 mg-which is higher than the 0.5 mg dose for treatment-naïve CHB patients-being applied to lamivudine-resistant CHB patients.276
In a study in which HBeAg-positive CHB patients were treated with 1.0 mg entecavir for 48 weeks, 19% of patients had an HBV DNA level of <300 cpm, 8% exhibited HBeAg seroconversion, the mean change in HBV DNA levels was -5.11 log10
cpm, and normalization of the ALT levels occurred in 61% of patients.277
Genotypic resistance to entecavir (7%) and accompanying virologic breakthrough (1.4%) were more frequent than in the treatment-naïve patients. When lamivudine-resistant CHB patients were treated with 1.0 mg entecavir for 2 years, HBV DNA was undetectable in 34% of patients, but an entecavir-resistant mutation that accompanied the virologic breakthrough occurred in 9% of patients.253
A 5-year cumulative rate of genotypic resistance of 51% was recently reported, along with an accompanying virologic breakthrough of 43%.254
Korean studies found that combination therapy of adefovir plus lamivudine showed superior antiviral efficacy over monotherapy with 1.0 mg entecavir in lamivudine-resistant CHB patients.278
Although 1.0 mg entecavir monotherapy exerts an initial favorable antiviral effect against HBV, it is not recommended as an optimal treatment in lamivudine-resistant CHB patients due to the associated high rates of resistance as it is considered to be inferior to combination therapy of adefovir plus lamivudine.
4) PegIFN monotherapy
PegIFN-α treatment could be considered in lamivudine-resistant CHB patients with compensated liver disease.280
One recent prospective Korean study of the effects of pegIFN found that the combined response rate (as assessed by HBeAg seroconversion, ALT-level normalization, and reduction of the HBV DNA level to <20,000 IU/mL) was 19% in lamivudine-resistant CHB patients and 12% in treatment-naïve subjects.280
Hence, pegIFN therapy can be considered in young patients with compensated liver disease, and it has beneficial effects in avoiding multidrug resistance caused by sequential oral nucles(t)ide analogue therapy.259
*When to change antiviral agents
When virologic breakthrough develops and genotypic resistance is found during lamivudine treatment despite good drug compliance, initiating rescue therapy is desirable before biochemical breakthrough develops.283
A study that enrolled CHB patients with genotypic resistance to lamivudine compared the effects of adding adefovir to lamivudine when the HBV DNA level was 3-6 log10
cpm and greater than 6 log10
cpm. The rates of undetectability of HBV DNA after 3 months (100% and 46%, respectively) and 2 years (100% and 78%) were higher in the earlier adefovir add-on group.283
A recent Korean study also found that a lower baseline HBV DNA level before initiating rescue therapy is associated with a favorable initial virologic response.392
The following options are recommended for the management of lamivudine resistance:
Add adefovir to lamivudine (A1).
Add tenofovir to lamivudine (B1).
Stop lamivudine and start adefovir or tenofovir in combination with one of the nucleoside analogues (C1).
Consider switching to tenofovir (B2).
Stop lamivudine and consider starting peginterferon if the patient has compensated liver function (B2).
2. Management of telbivudine resistance
Few data related to telbivudine resistance are available. A recent study found that adefovir rescue therapy is effective at reducing serum HBV DNA levels in telbivudine-resistant HBV infection.284
Tenofovir could be a therapeutic option, and its combination with nucleoside analogues would have the desirable effect of preventing subsequent antiviral resistance. The general principles for the management of telbivudine resistance can refer to the management of lamivudine resistance.
Telbivudine resistance: Refer to the management of lamivudine-resistant CHB (C1).
3. Management of clevudine resistance
At present it seems reasonable to treat clevudine resistance according to the principles of lamivudine resistance. A recent multicenter study in Korea compared the antiviral efficacies of adefovir monotherapy, combination therapy of adefovir plus lamivudine, combination therapy of clevudine plus adefovir, and entecavir monotherapy in clevudine-resistant CHB patients, and found that adefovir monotherapy showed the lowest antiviral efficacy at 12 weeks.285
However, long-term follow-up data are lacking. It is considered that the general treatment principles of clevudine resistance can follow those of lamivudine resistance.
Clevudine resistance: Refer to the management of lamivudine-resistant CHB (C1).
4. Management of adefovir resistance
The drugs listed below have been found to be effective at suppressing replication in adefovir-resistant HBV.
Tenofovir significantly suppresses HBV replication in patients exhibiting lamivudine resistance who have failed to respond adequately to adefovir, and in patients who are resistant to both lamivudine and adefovir.286
However, reduced sensitivity to tenofovir was demonstrated in adefovir-resistant HBV infections, indicating potential cross-resistance.273
Therefore, adding emtricitabine or lamivudine to tenofovir would be a more-appropriate therapeutic strategy than tenofovir monotherapy in patients exhibiting adefovir resistance. Indeed, the addition of emtricitabine led to a further decrease in the serum HBV DNA level in patients exhibiting adefovir resistance and a suboptimal response to tenofovir therapy.287
When combination therapy of lamivudine plus tenofovir was given to CHB patients who had previously failed in both lamivudine and subsequent adefovir therapy, 64% achieved an undetectable level of HBV DNA (<15 IU/mL) after 96 weeks of treatment.286
Recent studies have found that entecavir is effective at suppressing the replication of HBV in patients exhibiting adefovir resistance. Entecavir has been shown to be effective against both rtA181T/V and rtN236T mutant HBV strains,256
as entecavir does not share cross resistance with adefovir.252
A recent Korean study found that the mean reduction in serum HBV DNA levels was significantly greater in the entecavir-monotherapy group than in the lamivudine-plus-adefovir combination-therapy group among patients with sequential lamivudine-adefovir resistance (-3.47 vs. -1.49 log10
IU/mL, respectively; P
However, combination therapy of adefovir plus entecavir is considered a better therapeutic option because the selection of lamivudine-resistant strains during entecavir monotherapy can result in subsequent entecavir resistance.267
Combination therapy of entecavir and tenofovir can also be considered for multidrug-resistant HBV infections that include adefovir resistance.292
The rtN236T mutant was found to remain sensitive to lamivudine, while the rtA181/V mutant exhibited reduced susceptibility to lamivudine.252
When adefovir resistance develops in patients who received adefovir as an initial antiviral agent, switching from adefovir to lamivudine can be considered, but this may lead to subsequent lamivudine resistance. Therefore, combination therapy of lamivudine plus adefovir is recommended.
4) Telbivudine and clevudine
No study has evaluated telbivudine or clevudine as a rescue therapy for adefovir. However, it is thought that these drugs can be used in patients who do not exhibit resistance to nucleoside analogues because the rtN236T mutant remains sensitive to telbivudine or clevudine.252
However, telbivudine or clevudine is not recommended for the rtA181T/V mutant due to the possibility of cross-resistance.252
The following options are recommended for the management of adefovir resistance:
When adefovir has been used as the second drug after failure of L-nucleoside analogues
1) Stop adefovir and start combination therapy of tenofovir plus a nucleoside analogue (lamivudine or entecavir 1 mg) (B1).
2) Adding entecavir 1 mg to adefovir can be considered (B2).
When adefovir has been used as a first-line therapy
1) Stop adefovir and start combination therapy of tenofovir plus a nucleoside analogue (lamivudine or entecavir) (B1).
2) Consider adding a nucleoside analogue. If rtA181T is detected, adding entecavir is preferred (C1).
5. Management of entecavir resistance
The drugs listed below have been found to be effective at suppressing replication in entecavir-resistant HBV.
There are few data on the use of adefovir for treating entecavir resistance. Entecavir-resistant HBV is associated with lamivudine-resistant mutations, so treatment options may not differ in treatment-naïve patients and in lamivudine-resistant patients before the initiation of entecavir. Entecavir-resistant HBV maintains the susceptibility to adefovir, which could be considered as an initial treatment option, and a clinical case indicated that adefovir was effective in suppressing the entecavir-resistant mutant.293
Adding adefovir to entecavir would be more reasonable for reducing adefovir resistance and improving the antiviral efficacy.267
Combination therapy of adefovir plus lamivudine could be considered as another option, since a small study showed that the short-term efficacy of this combination was similar to that of combination therapy of adefovir plus entecavir.295
Tenofovir has not been fully evaluated in the treatment of entecavir resistance. However, it is expected that it will be very effective once it becomes available in Korea, since tenofovir does not show cross-resistance to entecavir in vitro
and has excellent potency.273
Entecavir resistance: Add a nucleotide analogue (tenofovir or adefovir) (B1).
6. Management of tenofovir resistance
There have been very few reports of clinical cases of tenofovir resistance. An in vitro
study found that replication of the rtA194T mutant was suppressed effectively by entecavir and intermediately by telbivudine.296
7. Management of multidrug resistance
Multidrug resistance is defined as resistance to two or more groups of antiviral drugs. Sequential monotherapy is associated with the development of multidrug resistance.259
For example, multidrug resistance may emerge if additional antiviral resistance develops in cases of (1) re-administration of lamivudine to prior lamivudine-resistant CHB patients receiving adefovir due to newly developed resistance to adefovir, (2) administration of entecavir to patients exhibiting lamivudine resistance, and (3) administration of lamivudine to patients exhibiting adefovir resistance, even in the absence of prior lamivudine treatment. In these situations, pre-existing antiviral resistant mutations may reappear and become co-located with newly developed resistant mutations on the same viral genomes.259
Combination therapy of tenofovir plus entecavir can be considered for resistance to both lamivudine and adefovir.243
Combination therapy of adefovir plus entecavir could be another option.267
If resistant mutations to lamivudine, entecavir, and adefovir are detected at the same time, combination therapy of tenofovir plus entecavir might be the best option.292
The following options are recommended for the management of multidrug resistance:
Combine tenofovir and entecavir 1 mg (B1).
Consider combining adefovir and entecavir 1 mg (B2).
Response-Guided Therapy During Oral Antiviral Drug Treatment for Hepatitis B
Once antiviral-resistant HBV mutants have been selected, they are persistently archived (retained in the virus population) in cccDNA in the nucleus of infected cells, even if treatment is stopped, and thereby potentially limiting future therapeutic options.298
Preventing the development of resistance is important to ensure the long-term therapeutic efficacy. The persistence of viral replication during antiviral treatment is associated with the emergence of drug resistance.235
Therefore, evaluating the treatment response by using sensitive PCR assays to measure serum HBV DNA levels every 3 months is recommended.
The rate of emergence of lamivudine-resistant HBV was directly proportional to the HBV DNA level after 24 weeks of treatment.235
Yuen and colleagues found that these rates were 8%, 13%, 32%, and 64% for patients with 24-week HBV DNA levels of <200, 3 log10
, 4 log10
, and 4 log10
cpm or higher, respectively, after a median follow-up of 29 months.300
This finding has been supported by several subsequent studies. Fukai and colleagues found that patients who achieved an undetectable HBV DNA level in PCR tests at week 24 of lamivudine treatment exhibited a substantially lower rate of virologic breakthrough.301
The importance of HBV DNA suppression at week 24 has also been shown in a phase-3 multicenter trial with telbivudine (the GLOBE trial).235
Therefore, an on-treatment strategy for patients receiving oral NUC therapy will produce better viral suppression and lower drug resistance by measuring serum HBV DNA levels at 24 weeks (Fig. 1
Patients with primary treatment failure-defined as a reduction in the serum HBV DNA level of less than 2 log10
IU/mL at week 24 with good drug compliance-should be tested for the presence of genotypic resistance mutations. If such mutations are not found, switching to a drug with a high genetic barrier is indicated if the patient is taking a drug with a low genetic barrier.289
The risk of resistance development in patients with a complete virologic response-defined as an HBV DNA level that is undetectable in PCR tests (less than 60 IU/mL or 300 cpm) at week 24-is low during long-term treatment.235
Thus, treatment should be continued until the treatment endpoint is achieved, with the serum HBV DNA level being measured every 3-6 months.126
A partial virologic response is defined as detectable HBV DNA without primary treatment failure at week 24. Up to 30% of the cases of virologic breakthrough observed in clinical trials are related to medication noncompliance.304
Thus, compliance should be ascertained before testing for genotypic resistance.
A recent European multicenter cohort study found that the antiviral efficacy of entecavir did not differ between patients who did not develop lamivudine resistance following lamivudine treatment and lamivudine-naive patients.289
A recent Korean multicenter clinical trial also showed that switching patients with insufficient suppression of HBV replication (HBV DNA ≥60 IU/mL) to entecavir (1 mg/day) resulted in a significantly higher proportion of patients with serum HBV DNA levels that were undetectable in real-time PCR at week 48 relative to those who continued lamivudine (77.3% vs. 8.7%, respectively). No patients in the entecavir-switch group developed resistance, while genotypic resistance emerged in 60.9% (14/23) of patients in the lamivudine-maintained group during the 48 weeks of treatment.302
The response to tenofovir monotherapy was not influenced by the presence of lamivudine resistance.273
Most NUC-naïve patients with detectable HBV DNA during entecavir or tenofovir therapy achieved undetectable levels of HBV DNA after prolonged continuation of entecavir or tenofovir monotherapy, and none of them developed additional drug resistance.159
Therefore, three options should be considered for patients with a partial virologic response: (1) if the patient is taking a drug with a low genetic barrier (e.g., lamivudine, telbivudine, clevudine, or adefovir), he/she should be switched to a high-genetic-barrier drug (e.g., entecavir or tenofovir); (2) if the patient is taking a drug with a high genetic barrier, treatment should be continued with regular monitoring for viral breakthrough; and (3) if viral breakthrough is detected, a rescue therapy should be implemented according to the results of the genotypic resistance analysis. In any case, the treatment strategy should follow the recommendations for drug-resistant HBV when genotypic resistance mutations are identified.
Patients with primary treatment failure and good drug compliance should be tested for the presence of genotypic resistance mutations. In the absence of genotypic resistance mutations, switching to a drug with a high genetic barrier is indicated if the patient is taking a drug with a low genetic barrier (B1).
In patients with a complete virologic response at week 24, treatment should be continued until the treatment endpoint is achieved, with the serum HBV DNA level being measured every 3-6 months (B1).
For patients with a partial virologic response at week 24 and good drug compliance, the following three options should be considered:
1) If the patient is taking a drug with a low genetic barrier (e.g., lamivudine, telbivudine, clevudine, or adefovir), treatment should be switched to a high-genetic-barrier drug (e.g., entecavir or tenofovir) (B1).
2) If the patient is taking a drug with a high genetic barrier, treatment should be continued with regular monitoring for viral breakthrough (B1).
3) In the event of viral breakthrough, a rescue therapy should be implemented according to the results of the genotypic resistance analysis (A1).
The treatment strategy should follow the recommendations for drug-resistant HBV when genotypic resistance mutations are identified (A1).
TREATMENT OF SPECIAL POPULATIONS
Acute hepatitis B
It is well known that acute hepatitis B recovers spontaneously and does not progress to chronic stage in more than 95%, so antiviral therapy is generally not recommended.308
There have been reports showing early initiation of antiviral therapy interferes with normal protective immune response and suppresses production of neutralizing antibodies against hepatitis virus, therefore increasing the risk of chronic hepatitis.310
However, acute hepatitis B infection seldom progress to serious hepatitis and may even fall into hepatic failure.309
According to a randomized controlled trial in 71 patients with severe acute hepatitis B, HBV DNA levels were significantly lower in lamivudine treated group (n=31, 3.7 log10
copies/mL) compared with control group (n=40, 4.2 log10
copies/mL) after 4 weeks. However, negative conversion rate of HBsAg after 12 months was similar between the two groups (93.5% in lamivudine group and 96.7% in placebo group).312
In this study, development of protective anti-HBs after 1 year, was 67.7% in the lamivudine group and 85% in the placebo group, but it was not statistically significant. Tillman et al reported that lamivudine is safe in patients with severe acute or fulminant hepatitis B, leading to fast recovery with the potential to prevent liver failure and liver transplantation when administered early enough.313
There have been only a few case reports of antiviral agents as treatment for acute hepatitis B other than lamivudine so far.314
In patients with acute hepatitis B, oral antiviral therapy should be considered in cases of persistent serious hepatitis or acute liver failure. (C1)
Liver Transplant Patients
For most patients with liver disorders related to HBV, the recurrence of HBV causes severe liver damage. Moreover, the survival rate of such patients has been low in the past.317
In an extensive cohort study of 372 patients who received liver transplants in the early 1990s and were positive for HBsAg, the test group treated with hepatitis B immunoglobulin (HBIG) therapy for more than 6 months showed a significantly lower recurrence rate of hepatitis B than the group treated with HBIG therapy for less than 6 months or those who were not treated with this therapy. The test group also had a higher long-term survival rate than the other groups.325
Since then, several studies have reported hepatitis B recurrence rates ranging from 16% to 35% after liver transplantation in groups receiving high-dose HBIG (10,000 IU) therapy.326
For the patients who received lamivudine monotherapy, the recurrence rate of hepatitis B was approximately 40% 4 years after liver transplantation, and the emergence of lamivudine resistance mutants has also been reported. Therefore, the effectiveness of therapy using only lamivudine is limited.329
On the other hand, a study using lamivudine and adefovir combination therapy reported no recurrence in patients with hepatitis B during a 1-year observation period, although these studies had limited scope. In this study, lamivudine resistance was also prevented.331
Further studies are therefore required on combination therapy using antiviral agents to prevent the recurrence of hepatitis B. Lamivudine and HBIG combination therapy could reduce the recurrence of HBV to less than 10% in 1-2 years and is superior to high-dose HBIG therapy with respect to cost and effectiveness.332
In a meta-analysis of 6 independent studies, lamivudine and HBIG combination therapy was found to reduce the recurrence rate of HBV and relevant death rate by 12 times compared with HBIG therapy alone.336
In a study of 147 patients who received liver transplants, Gane et al. showed that lamivudine and low-dose HBIG (400-800 IU) combination therapy effectively suppressed the recurrence of hepatitis B at moderate cost, since the 5-year recurrence rate of hepatitis B was only 4%.337
Furthermore, the patients whose HVB DNA was less than 2.5 pg/mL before liver transplant were randomly assigned to continuing combination therapy and lamivudine monotherapy groups after administering lamivudine and HBIG (2,000 IU) combination therapy after liver transplants for 18 months, resulting in no difference in the rates of HBV recurrence and patient survival during a median follow-up of 83 months between the two groups in this prospective study.338
Two other retrospective studies have reported no recurrence of HBV when lamivudine and HBIG combination therapy or HBIG therapy alone for 2 years after liver transplantation were replaced with lamivudine monotherapy.339
In a recent study by Angus et al., lamivudine and low-dose HBIG (800 IU) combination therapy was continued for at least 12 months after liver transplantation. The group in which HBIG was replaced by adefovir and the group in which HBIG was continuously administered did not show a difference in the recurrence rate of hepatitis B.341
These results suggest the possibility of reducing the period of high-dose HBIG administration, which is expensive. However, it is estimated that the combination therapy would be applied to clinical cases provided that its long-term effects are recognized through extensive future research.
A meta-analysis of 46 studies in which 2,161 HBV-infected patients received liver transplants found that adefovir and HBIG combination therapy significantly reduced the recurrence rate of hepatitis B to 2% compared to 6% with lamivudine and HBIG combination therapy. A preliminary study that was conducted recently has confirmed the good results of HBIG combination therapy with entecavir or tenofovir, which has strong anti-viral effects and less drug resistance. Consequently, it is expected that these drugs will be used more efficiently in the future.342
Meanwhile, a study by Grellier et al. has indicated that when lamivudine therapy is administered from 4 weeks before liver transplantation, the recurrence of HBV after the transplant is effectively prevented.343
A recent prospective study found that in 57 patients with lamivudine-resistant HBV who were treated with lamivudine plus adefovir, only two (3.5%) had HBV recurrence for a median of 9 months with a survival rate of 87%.344
However, the impacts of entecavir and tenofovir therapy before liver transplantation on the recurrence of HBV after liver transplants remain unreported, and thus require further examination.
When hepatitis B recurs even after preventive HBIG therapy after liver transplantation, lamivudine therapy could effectively inhibit the virus. However, it has been reported that lamivudine resistance was over 50% over 3 years when lamivudine therapy is administered over a long term.345
It is known that such lamivudine resistance causes inflammatory changes in the transplanted liver and hepatic fibrosis, and severe impacts, including death, by hepatic failure.346
A few studies have reported the effects of tenofovir and entecavir on hepatitis B recurrence after liver transplantation; however, more studies on these drugs need to be performed.350
Several studies have reported the relatively good effects of lamivudine and adefovir on patients with recurrent hepatitis B who exhibit lamivudine resistance after liver transplantation. The most extensive study administered the combination therapy to 241 patients with recurrent hepatitis B. The HVB DNA reduction rate was 65%, whereas lamivudine resistance 96 weeks after therapy started was 2%.344
Although these studies were conducted for a short period with small groups, it was recently reported that tenofovir is effective against mutants with lamivudine resistance.349
However, high emergence rate of entecavir resistance have been reported when entecavir is administered as rescue therapy for patients who had lamivudine resistance.254
Therefore, entecavir is not recommended if patients have lamivudine resistance after liver transplantation.
It is known that if negative HBsAg patients receive liver transplants from positive anti-HBc donors, approximately 50% will have new hepatitis B.351
When HBIG therapy was administered to these patients after liver transplantation, hepatitis B affected over 20%. However, when lamivudine therapy was applied, hepatitis B affected only 2-3% of patients. Nevertheless, lamivudine and HBIG combination therapy had no additional preventive effects compared to lamivudine therapy alone.351
There has been no research on anti-viral drugs other than lamivudine.
For patients whose serum is positive for HBV DNA and who have had a liver transplant, the serum HBV DNA value should be minimized before liver transplantation by administering oral anti-viral drugs (A1).
The anti-viral therapy before liver transplantation complies with the chronic hepatitis B therapy guidelines (B1).
Oral anti-viral drugs and HBIG therapy should be administered throughout life to prevent the recurrence of hepatitis B after liver transplantation (B1). However, if serum HBV DNA is positive before the liver transplant, HBIG may not be administered to the patients after long-term monitoring (B2).
In case of HBV recurrence after liver transplantation, antiviral drugs that strongly suppress viruses and have low drug resistance are recommended (A1). In case of drug resistance, the chronic hepatitis B therapy guidelines are followed (B1).
Immunosuppression and Chemotherapy
Impaired host immunity due to chemotherapy or immunosuppressive treatment increases the risk of HBV reactivation.354
HBV reactivation refers to the reappearance of necroinflammatory disorders in patients with either inactive carrier or resolved hepatitis,355
and is commonly defined as a rise in the serum HBV DNA of more than 10 times of the baseline level or an absolute level of higher than 100 IU/mL along with elevated serum ALT (higher than 3 X ULN or an absolute increase of more than 100 IU/L).356
The diagnosis of HBV reactivation requires the exclusion of other conditions such as chemotherapy-related hepatic injury, hepatic metastases, and other types of viral hepatitis. The reactivation rate has been reported as 20-50%, although the ranges were diverse in various reports. Many patients with HBV reactivation are asymptomatic, but the clinical courses are varied widely from jaundice to decompensation or even death.356
In typical cases, HBV DNA appears in the serum during immunosuppressive treatment, followed by elevation of ALT after treatment cessation. If HBV reactivation occurs during chemotherapy, treatment disruption or premature termination may adversely affect the outcome of chemotherapy.361
Predictive factors for HBV reactivation include the pretreatment HBV DNA level, type of malignancy, and type or intensity of immunosuppression or chemotherapy. The reported reactivation rate in lymphoma patients has ranged from 24% to 67%, possibly due to intense chemotherapeutic regimens against lymphoma and higher positivity rates for HBsAg in these patients.359
Rituximab, which has been commonly administered with corticosteroid for lymphoma, further increases the risk of HBV reactivation.367
The risk of reactivation is also elevated when high-intensity chemotherapy is applied prior to hematopoietic stem-cell transplantation in hematologic malignancies.369
Although the reactivation rate has been known as 14-21% in solid tumors, higher rates of 41-56% were reported in breast cancer which is possibly related to the use of high dose chemotherapy and anthracycline agents.371
Sorafenib, which was approved recently for advanced HCC, seems not cause HBV reactivation,373
but this needs to be confirmed in further investigations. Corticosteroid increases the risk of HBV reactivation via immune suppression as well as direct stimulation of HBV replication. Other risk factors for reactivation include the use of anti-TNF-α antibody for inflammatory bowel diseases or rheumatologic diseases (e.g., infliximab), the HBV genotype or specific mutations on the HBV genome, and recovery from neutropenia.374
In rare cases, HBV reactivation occurs not only in HBsAg-positive patients but also in anti-HBc IgG-positive patients without HBsAg.384
The latter cases correspond to either occult HBV infection in which HBV DNA is detected in the hepatocytes or even in the serum, or reverse seroconversion (seroreversion) of HBsAg in which HBV replication resumes after immunosuppression with reappearance of HBsAg.356
Because HBV reactivation is associated with the risk of hepatic failure or even death once it occurs, prevention is of utmost importance. This makes screening for HBsAg and anti-HBc IgG is necessary. Vaccination should be considered if there is no evidence of (past) HBV infection (i.e., negative for both HBsAg and anti-HBc IgG). Preemptive antiviral therapy is recommended in HBsAg-positive patients regardless of the serum HBV DNA level.376
Preemptive lamivudine therapy has significantly reduced the rates of HBV reactivation, hepatic failure, and mortality in randomized controlled studies of lymphoma patients in Hong Kong and Taiwan.365
From these results, it is recommended that preemptive antiviral therapy should be started with the initiation of chemotherapy rather than deferring until the HBV DNA level increases, and should be maintained for certain period after the termination of chemotherapy (e.g., at least 6 months).388
However, evidence to determine the duration of preemptive antiviral therapy remains limited. Elevated risk of reactivation was reported with cessation of preemptive lamivudine therapy after 3 months following the termination of chemotherapy, especially in cases of a high HBV DNA before chemotherapy (≥2,000 IU/mL).390
Therefore, the duration of preemptive antiviral therapy could be determined based upon treatment guidelines for CHB if the pre-treatment HBV DNA level is high. In contrast, special attention should be paied to reports of reactivation after more than 6 months irrespective of the pre-treatment HBV DNA level. Although there is limited information about the efficacy of preemptive treatment with other antiviral agents such as adefovir, tenofovir, entecavir, telbivudine, or clevudine, these agents could be administered for preemptive use considering their mechanisms of action and therapeutic results. Since resistance was reported in preemptive lamivudine therapy, other antiviral agents with lower resistance rate need to be considered in cases with prolonged treatment period (e.g., longer than 1 year).365
A recent retrospective study demonstrated that the risks of hepatitis and chemotherapy disruption due to HBV reactivation in lymphoma patients were lower for entecavir than for lamivudine.391
However, data on the relative efficacy and cost-effectiveness of antiviral agents are scarce. Prospective studies of the appropriate choice of antiviral agents and optimal treatment duration in various types of malignancies are urgently needed, since most of the previous studies only included lymphoma patients. If cost is ignored, entecavir and tenofovir will be safer choices based on their potency and resistance rate. Interferon-α is contraindicated for preemptive use due to its bone marrow suppression and exacerbation of underlying hepatitis. Anti-HBc IgG-positive patients (HBsAg-negative) have a risk of HBV reactivation, but a uniform treatment recommendation cannot be provided because the effects of the types of malignancies or immunosuppressive/chemotherapeutic agents used on the reactivation risk has not been clarified. However, preemptive therapy should be considered if serum HBV DNA is positive in high-risk groups such as patients with lymphoma under a rituximab-containing regimen or those with leukemia who undergo hematopoietic stem cell transplantaion; the need for preemptive treatment may be determined with periodic monitoring (e.g., every 1-2 months) of the HBV DNA level in patients with no detectable serum HBV DNA at baseline.
Check HBsAg and anti-HBc IgG before starting immunosuppressive treatment or chemotherapy. (A1)
Vaccinate if there is no evidence of HBV infection. (B1)
Consider preemptive antiviral therapy with the initiation of immunosuppressive treatment/chemotherapy if HBsAg is positive. (A1) Although the choice of antiviral agent requires consideration of the serum HBV DNA level, intensity and duration of immunosuppressive treatment/chemotherapy and cost, entecavir or tenofovir can be preferentially considered if the baseline HBV DNA level is high or long-term treatment is needed. (C1)
The serum HBV DNA should be monitored periodically during and after preemptive antiviral therapy. (A1)
Preemptive antiviral therapy has to be maintained for at least 6 months after terminating immunosuppressive treatment/chemotherapy. (C1)
In anti-HBc IgG-positive patients, preemptive therapy should be considered if serum HBV DNA is detectable in high-risk groups (C1). The need for preemptive treatment may be determined by periodic monitoring of the HBV DNA level in patients with no detectable serum HBV DNA at baseline. (C2)
Dialysis patients are relatively prone to being exposed to HBV infection, which might exert negative influence on their long-term prognosis. Exacerbation of hepatitis B is of particular importance to immunosuppresion after renal transplantation.392
Fortunately, the incidence of HBV infection in dialysis patients has reduced thanks to surveillance of blood products, enhanced infection control, and widespread use of erythropoietin. The prevalence of HBV infection based on HBsAg positivity in this population is known as 0-6.6% in Western countries, and approximately 5% in Korea in recent reports.393
Prevalence of occult HBV infection was higher than HBsAg-positive rate in some reports,396
but this was not the case in Korea.397
The standard precaution to avoid nosocomial transmission is of the highest priority for preventing new HBV infections in dialysis patients.398
Vaccination against HBV is widely recommended in these patients; the efficacy is higher with eariler vaccination because antibody production rate is as low as 50-60% compared with about 90% of general population and it is lower as residual renal function declines.399
Data on the antiviral treatment based in dialysis patients are insufficient. Although there is a randomized controlled study on interferon-α in HBV-infected patients with glomerulonephritis,402
it appears difficult to recommend its use considering the increased adverse events in this population due to pharmcodynamic changes.403
Several small studies reported the effectiveness of lamivudine.405
Resistance to lamivudine was as high as 39% at 16.5 months of treatment which was similar to patients with normal renal function,408
and adefovir can be added for lamivudine resistance.409
Entecavir or tenofovir may be preferentially used, given their potency and resistance profile in patients with normal renal function.37
Careful dose adjustment is required for adefovir and tenofovir due to their potential nephrotoxicity in patients with residual renal function.411
Vaccination is necessary in dialysis patients without anti-HBs. (A1)
Oral anvitiral agents are recommended rather than interferon in dialysis patients. (B1) Entecavir and tenofovir are preferentially considered according to the residual renal function. (B1)
Co-infection with other viruses
In patients with CHB the rate for anti-HCV antibody positivity varies from 0.1% to 22%, depending on the region,415
with it being very low in Korea (0.1%).416
Patients with HBV/HCV co-infection are known to have an increased risk of severe or fulminant infection, and high incidences of cirrhosis and HCC.419
The scarcity of data makes it impossible to recommend the treatment of HBV/HCV co-infection.423
However, it is necessary to determine which virus is dominant by means of serologic or virologic tests. It is recommended that CHB patients who are positive for HCV RNA are treated with combination therapy of pegIFN-α-2a plus ribavirin which has been shown to be equally effective in patients with HCV mono-infection and HBV/HCV co-infection.426
The HBV treatment should be added when HBV reactivates, which can reportedly occur during or after the standard treatment for HCV.427
Apply serologic or virologic tests to determine which virus is dominant (B1).
CHB patients with detectable HCV RNA should be treated with combination therapy of pegIFN-α-2a plus ribavirin (B1).
HBV treatment should be added when HBV reactivates, which can occur during or after the standard treatment for HCV (B1).
It is estimated that approximately 20 million people are infected with HDV worldwide.428
HDV infection is prevalent in Mediterranean countries, the Middle East, central Africa, and South America.429
The HDV co-infection rate in CHB patients has been reported to be 0-3.6% in Korea.430
The incidences of cirrhosis and HCC are known to be higher in patients with HBV/HDV coinfection than in those with HBV monoinfection.433
HDV infection can be diagnosed by detecting anti-HDV antibody or HDV RNA in the patient's serum or by detecting HDV antigen in liver tissue by immunohistochemistry. The treatment goals are to inhibit HDV replication, normalize ALT, and improve histology findings. IFN-α (conventional or pegylated) is the only drug that can inhibit HDV replication.435
The biochemical, virologic, and histologic responses were found to be better for high-dose IFN-α therapy (9 MU, three times per week) than for the conventional dose of IFN (3 MU, three times per week), with the high-dose therapy producing an HDV RNA negativity rate of 43% at 6 months after the end of 48 weeks of treatment.438
PegIFN-α showed HDV RNA negativity rates of 17-43% at 6 months after the end of 48 or 72 weeks of treatment.435
No head-to-head comparison trial between high dose IFN-α and pegIFN-α therapies has been performed and hence either pegIFN-α or high-dose IFN-α therapy for longer than one year is recommended for patients with HBV/HDV co-infection.441
The treatment response can be evaluated by measuring the serum HDV RNA level at week 24. Both lamivudine and adefovir were found to be ineffective at inhibiting HDV replication.442
Combination therapy of lamivudine plus IFN-α was not superior to IFN-α monotherapy,444
and adefovir plus pegIFN-α therapy also did not improve the response rate relative to pegIFN-α monotherapy.443
CHB patients with HDV co-infection should be treated with pegIFN-α or high-dose IFN-α (9 MU, three times per week) for longer than one year (B1).
The incidences of cirrhosis and HCC are reportedly higher in patients with HBV/HIV coinfection than in those with HBV monoinfection.445
Treating HBV should be considered in HBV/HIV-coinfected patients who exhibit ALT elevation due to HBV. Before such treatment it is necessary to determine whether or not treatment against HIV is also required.447
Patients who are not indicated for HAART should receive the standard treatment for CHB. In that case the antiviral agents should be chosen (e.g., IFN, adefovir, or telbivudine) on the basis that they will not affect HIV proliferation, in order to prevent the future development of HIV cross-resistance. Patients who need treatment for both HIV and HBV should be treated with antiviral agents that are effective against both viruses, such as lamivudine, tenofovir, or emtricitabine.448
When HAART regimens are altered, antiviral agents that are effective against HBV should be included to avoid HBV reactivation, except in patients who meet the criteria for discontinuation of anti-HBV treatment.
HBV/HIV-coinfected patients who exhibit ALT elevation due to HBV should be considered for HBV treatment (B1).
Patients who are not indicated for HAART at present or in the near future should receive the standard treatment for CHB. In that case the antiviral agents should be chosen on the basis that they will not affect HIV proliferation, in order to prevent the futuredevelopment of HIV cross-resistance (B1).
Patients who need treatment for both HIV and HBV should be treated with antiviral agents that are effective against both viruses (B1).
Female patients of childbearing age
Treatment before pregnancy
When planning the treatment for women of child-bearing age, special considerations for the fetus and the duration of treatment are needed in addition to the aforementioned general considerations. For example, IFN preparations are preferred in female patients who are planning pregnancy since the period of treatment is more clearly defined. However, the IFN side effect of fetal malformations makes it contraindicated during pregnancy, and so it must be recommended in combination with contraception.
Treatment during pregnancy
Changes in the maternal immune system during pregnancy such as a shift in the Th1-Th2 balance toward a Th2 response lead to an increase in the HBV DNA level and a reduction in the ALT level.451
These immune responses are restored after delivery, thereby causing a reduction of the HBV DNA level and ALT elevation, and so careful monitoring is needed.
The optimal antiviral treatment strategy during pregnancy is based on the aforementioned general principles for the treatment of CHB. However, all decisions about the timing and duration of treatment in pregnancy should include an analysis of the risks and benefits for both the mother and fetus. In addition, pregnant women often experience worsening of liver disease unrelated to HBV infection (e.g., acute fatty liver of pregnancy), which is difficult to discriminate from an HBV flare-up. Thus, antiviral treatment should be considered when the liver disease is present (e.g., jaundice or prolongation of PT), and the HBV DNA level meets general criteria for antiviral treatment.
When starting antiviral therapy during pregnancy, Category B drugs (which, according to the results of animal studies, carry no teratogenic or embryogenic risk and for which there have been no controlled human studies or for which animal studies may indicate a risk, but controlled human studies refute the findings) are recommended. Among oral antiviral agents, telbivudine, tenofovir, and emtricitabine are Category B drugs, while lamivudine, adefovir, and entecavir are Category C drugs (drugs that exert teratogenic or embryocidal effects in animals and for which there are no controlled studies in humans).19
The safety data of antiviral agents during pregnancy can be found at the Antiretroviral Pregnancy Registry (APR; http://www.apregistry.com
). The APR is an international, voluntary, prospective registry that reports the rate of birth defects of newborns born to mothers receiving antiretroviral therapy, and it contains a considerable amount of data on lamivudine and tenofovir. According to the APR, the rates of birth defects among women exposed to lamivudine and tenofovir in the first trimester (3.1% and 2.4% of live births, respectively) are similar to that in the general population (2.7%), as reported by the CDC birth defect surveillance system. There are only a few reported cases related to other drugs such as telbivudine and entecavir. However, since the APR is designed to report onlydefects identified at birth, it is possible that it does not contain accurate data on developmental anomalies (e.g., cardiac or neurologic defects).
Oral antiviral agents may cause mitochondrial toxicity by inhibiting mitochondrial DNA replication. It is difficult to estimate their effects on the fetus especially in the developmental stages.452
Thus, based on considerations of fetal safety it is desirable to avoid the administration of oral antiviral agents, especially in the first trimester of pregnancy. However, the decision about whether to discontinue drugs in patients who are already been treated with oral antiviral agents should be individualized; such patients may be considered for temporary drug discontinuation when the degree of liver disease is mild and the HBV DNA level is <60 IU/mL, but in that case they should be carefully monitored for HBV reactivation. Meanwhile, women who become pregnant while on Category C drugs should change to Category B drugs. Since little is known about whether or not antiviral agents are secreted into breast milk, breast-feeding is currently not recommended.
Prevention of vertical transmission with antiviral drugs
A high maternal HBV DNA level is known to be associated with a high failure rate of neonatal passive-active immunoprophylaxis.453
In a double-blind, randomized controlled trial, pregnant women with high serum HBV DNA levels [>103
cpm)] were given lamivudine from week 32 of gestation to week 4 postpartum in addition to neonatal passive-active immunoprophylaxis.455
HBsAg positivity was present in 18% and 39% of 1-year-old infants from lamivudine- and placebo-treated mothers, respectively (P
=0.014). No safety concerns were noted in the lamivudine-treated mothers and their newborns. However, these data should be interpreted with caution due to the high dropout rates, especially in the placebo group (13% in the lamivudine group and 31% in the placebo group). A prospective controlled study included pregnant women with high serum HBV DNA levels (>107
cpm) who were treated with telbivudine from weeks 20 to 32 of gestation to week 4 postpartum in addition to neonatal passive-active immunoprophylaxis.456
HBsAg positivity was present in none of the 6-month-old infants from telbivudine-treated mothers, whereas it was present in 8% of those from placebo-treated mothers. The prevalence of safety issues did not differ significantly between the two groups. These studies imply that antiviral medication in the late stage of pregnancy is likely to reduce the vertical transmission rate. However, the decision about whether or not to treat should be individualized in patients who are not indicated for the treatment of HBV, based on the treatment duration, stopping point, possible appearance of drug-resistant strains, and the patient's preferences.
PegIFN is preferred in female patients who are planning pregnancy since the period of treatment is more clearly defined (C1). However, the side effects of fetal malformations make pegIFN contraindicated during pregnancy, and so it must be recommended in combination with contraception (A1).
When antiviral treatment is needed during pregnancy, Category B drugs such as telbivudine or tenofovir are recommended (B1).
The antiviral treatment strategy during pregnancy is based on the general principles of treatment of CHB; however, decisions should be based on analysis of the risks and benefits for both the mother and fetus (C1).
Breast-feeding is not recommended in women who are treated with antiviral agents (C1).
Children and adolescents
Providing HBIG and HBV vaccine to newborns of HBsAg-positive mothers within 12 hours of birth can prevent 90-95% of cases of perinatal infection. Ninety percent of infants infected as a neonate progress to chronic infection. Most children remain in the immune-tolerant phase until late childhood or adolescence. However, some children progress to the immune-reactive phase. A Taiwanese study found that the annual spontaneous HBeAg seroconversion rates were 2% and 4-5% in children younger than 3 years and older than 3 years, respectively.457
Children who are in the immune-reactive phase-with increased ALT levels and histologic findings of liver inflammation and fibrosis-are usually asymptomatic. The goals of therapy are to suppress viral replication, reduce liver inflammation, reverse liver fibrosis, and prevent cirrhosis and HCC.
Treating children in the immune-tolerant phase is not beneficial, and there is a high risk of the development of drug resistance, which would limit the treatment options in later life. Children with a persistent elevated serum ALT should be evaluated for viral active replication, including measurement of HBV DNA levels. HBeAg-positive children should be considered for treatment when their serum ALT levels are above 2× ULN for at least 6 months and their HBV DNA levels are above 20,000 IU/mL.458
Acute elevation of the liver enzymes with an ALT level of >5× ULN may be followed by spontaneous HBeAg seroconversion. It is therefore reasonable to delay treatment for an observation period of at least 3 months if there is no concern about hepatic decompensation. Children with moderate-to-severe necroinflammation or periportal fibrosis in a liver biopsy are recommended for treatment. The decision to treat is based on factors such as age, liver biopsy findings, and family history of HBV-associated cirrhosis or HCC. In obese children it is important to remember that ALT elevations may be due to fatty liver disease.459
The responses to interferon-α and lamivudine are better in children with higher activity scores in a liver biopsy.460
There are few data on the drugs prescribed to children and adolescents younger than 18 years. Drugs that have been shown to be effective in randomized controlled trials are interferon-α, lamivudine, and adefovir. Entecavir is labeled for those aged 16 years and older.
A randomized controlled trial of interferon-α therapy involving children aged 1 to 17 years found that 36% of treated children whose baseline ALT was at least 2× ULN became negative for HBeAg at the end of treatment. HBsAg seroconversion occurred in 10% of the children in the treatment group.460
Factors that are predictive of a positive response among children are being younger than 5 years,462
having a low serum HBV DNA level, and having active inflammation in a liver biopsy.460
After 5 years of observation the rate of HBeAg seroconversion did not differ between the treatment and control groups. However, loss of HBsAg occurred in 25% of children who responded during treatment, but in none of the children in the nonresponse and control groups.463
The recommended treatment regimen for interferon-α is 6 MU/m2
three times per week by subcutaneous injection for 6 months. Interferon-α is approved in children older than 12 months, and its advantages include the finite duration of treatment and no development of viral resistance. The adverse effects include fever, flu-like symptoms, bone marrow suppression, depression, and transient growth suppression. Interferon-α is contraindicated in children with decompensated cirrhosis and autoimmune disease. There are no published reports on clinical trials of peginterferon in children with CHB. However, the efficacy and safety of peginterferon were demonstrated for treating children with chronic hepatitis C, and a recent update of the Swedish national recommendations for the treatment of CHB recommends the use of peginterferon (100 µg/m2
weekly) in children.464
A randomized controlled study of lamivudine involving children aged 2-17 years found that loss of HBeAg at 52 weeks of treatment occurred in 34% of children whose baseline ALT level was at least 2× ULN, and that the resistance rate was 18%.465
The HBeAg seroconversion rate after 2 years of therapy was 54% in children without lamivudine-resistant viruses. The resistance rate was 64% in children who received lamivudine for 3 years. Lamivudine treatment over 3 years did not significantly increase seroconversion rates and it increased the incidence of viral resistance.466
Studies of Korean children found that the HBeAg seroconversion rates after 2 and 3 years of treatment were 65% and 70%, respectively.467
Loss of HBsAg was observed in 20% of children after 2 years of lamivudine treatment, and the resistance rates at 1 and 2 years of treatment were 10% and 23%, respectively. Factors associated with a response were elevated baseline ALT, high baseline histology-activity-index score,461
and being younger than 7 years.467
Long-term durability of HBeAg seroconversion was observed in more than 90% of the subjects after they had taken lamivudine for at least 2 years.469
Lamivudine is orally administered at a dose of 3 mg/kg/day, with a maximum of 100 mg/day. Adefovir could be added if there is incomplete suppression after 24 weeks of therapy, or the treatment could be changed to off-label entecavir.459
Lamivudine treatment should be continued for at least 1 year, and it is desirable to continue treatment for 1 year after HBeAg seroconversion. Adefovir should be added when lamivudine resistance develops.
Another randomized controlled study of HBeAg-positive children aged 2-17 years showed undetectable HBV DNA and a normal ALT level after 48 weeks of adefovir treatment in 23% of the 12-to 17-year-old subjects, but there was no statistical difference between adefovir and placebo in the subjects aged 2-11 years.470
No subject developed adefovir resistance.
Entecavir and tenofovir are potent HBV inhibitors with a high barrier to resistance. Pediatric clinical trials of entecavir and tenofovir are currently underway, and if the final results are positive they will be suitable for use in therapies. Entecavir is considered a first-line therapy for adolescents aged 16 years and older. Therapeutic options for children are currently limited, and a prudent decision should be made based on the drug adverse effects and the potential for viral resistance to affect future therapies.
Children with HBeAg-positive CHB should be considered for treatment when the serum HBV DNA level is >20,000 IU/mL and the AST or ALT level is >2× ULN for at least 6 months, or moderate-to-severe necroinflammation or periportal fibrosis is shown in a liver biopsy (A1).
Lamivudine or interferon-α is considered the first-line therapy in children with CHB, while entecavir is the first-line therapy in those aged 16 years and older (B1). Data on peginterferon, entecavir, and tenofovir are currently scarce, but the use of these drugs in children can be based on the results obtained in studies involving the treatments administered to adults (C1).
If lamivudine resistance develops, adefovir should be added (A1).
American Association for the Study of Liver Diseases
Appraisal of Guidelines for Research and Evaluation II
hepatitis A virus antibody
hepatitis B core antibody
hepatitis B envelop antibody
hepatitis B surface antigen
Antiretroviral Pregnancy Registry
covalently closed circular DNA
Center for Disease Control
Clinical Practice Guideline Revision Committee
European Association for the Study of the Liver
Grading of Recommendations, Assessment, Development and Evaluation
highly active antiretroviral therapy
Hepatitis B envelop Antigen
Hepatitis B immunoglobulin
hepatitis B surface antigen
human immunodeficiency virus
The Korean Association for the Study of the Liver
polymerase chain reaction
Risk Evaluation of Viral Load Elevation and Association Liver Disease/Cancer-Hepatitis B Virus
upper limit of normal
1. Guyatt GH, Oxman AD, Vist GE, Kunz R, Falck-Ytter Y, Alonso-Coello P, et al. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ 2008;336:924-926. 18436948.
2. Guyatt GH, Oxman AD, Kunz R, Vist GE, Falck-Ytter Y, Schunemann HJ. What is "quality of evidence" and why is it important to clinicians? BMJ 2008;336:995-998. 18456631.
3. Guyatt GH, Oxman AD, Kunz R, Falck-Ytter Y, Vist GE, Liberati A, et al. Going from evidence to recommendations. BMJ 2008;336:1049-1051. 18467413.
4. Schünemann HJ, Oxman AD, Brozek J, Glasziou P, Jaeschke R, Vist GE, et al. Grading quality of evidence and strength of recommendations for diagnostic tests and strategies. BMJ 2008;336:1106-1110. 18483053.
6. Brouwers MC, Kho ME, Browman GP, Burgers JS, Cluzeau F, Feder G, et al. Development of the AGREE II, part 2: assessment of validity of items and tools to support application. CMAJ 2010;182:E472-E478. 20513779.
7. Song IS, Kim CY. Seasonal and annual variations on occurrence of HBsAg and acquisition of anti-HBs in Korea. Korean J Intern Med 1979;22:1007-1015.
8. Ahn YO. A review study on descriptive epidemiology of HBs antigen positivity in Korea. Korean J Epidemiol 1982;4:35-45.
9. Sim JG, Seo JK, Suh SJ. Prevalence and its changes of hepatitis B viral markers from 1988 to 1993 in Korean children. J Korean Pediatr Soc 1995;38:1535-1539.
10. Korea Centers for Disease Control and Prevention. 2006 Disease Control White Paper. 2007. Korea Centers for Disease Control and Prevention; p. 144.
11. Ministry of Helalth & Welfare. Korea Centers for Disease Control and Prevention. The Third Korea National Health and Nutrition Examination Survey (KNHANES III), 2005: Health Examination. 2006. Ministry of Helalth & Welfare; p. 68.
12. Chae HB, Kim JH, Kim JK, Yim HJ. Current status of liver diseases in Korea: hepatitis B. Korean J Hepatol 2009;15(Suppl 6):S13-S24. 20037275.
13. Cheon JH, Park JW, Park KW, Kim YI, Kim SH, Lee WJ, et al. The clinical report of 1,078 cases of hepatocellular carcinomas: National Cancer Center experience. Korean J Hepatol 2004;10:288-297. 15613804.
14. Kim SR, Kudo M, Hino O, Han KH, Chung YH, Lee HS. Epidemiology of hepatocellular carcinoma in Japan and Korea. A review. Oncology 2008;75(Suppl 1):13-16. 19092267.
16. Kim H, Jee YM, Song BC, Shin JW, Yang SH, Mun HS. Molecular epidemiology of hepatitis B virus (HBV) genotypes and serotypes in patients with chronic HBV infection in Korea. Intervirology 2007;50:52-57. 17164558.
17. Lee JM, Ahn SH, Chang HY, Shin JE, Kim DY, Sim MK, et al. Reappraisal of HBV genotypes and clinical significance in Koreans using MALDI-TOF mass spectrometry. Korean J Hepatol 2004;10:260-270. 15613801.
18. Lok AS, McMahon BJ. Chronic hepatitis B. Hepatology 2007;45:507-539. 17256718.
19. Hoofnagle JH, Doo E, Liang TJ, Fleischer R, Lok AS. Management of hepatitis B: summary of a clinical research workshop. Hepatology 2007;45:1056-1075. 17393513.
20. Lok AS, Lai CL. A longitudinal follow-up of asymptomatic hepatitis B surface antigen-positive Chinese children. Hepatology 1988;8:1130-1133. 3417235.
21. Chang MH, Hsu HY, Hsu HC, Ni YH, Chen JS, Chen DS. The significance of spontaneous hepatitis B e antigen seroconversion in childhood: with special emphasis on the clearance of hepatitis B e antigen before 3 years of age. Hepatology 1995;22:1387-1392. 7590652.
22. Hui CK, Leung N, Yuen ST, Zhang HY, Leung KW, Lu L, et al. Natural history and disease progression in Chinese chronic hepatitis B patients in immune-tolerant phase. Hepatology 2007;46:395-401. 17628874.
23. Livingston SE, Simonetti JP, Bulkow LR, Homan CE, Snowball MM, Cagle HH, et al. Clearance of hepatitis B e antigen in patients with chronic hepatitis B and genotypes A, B, C, D, and F. Gastroenterology 2007;133:1452-1457. 17920063.
24. Vierling JM. The immunology of hepatitis B. Clin Liver Dis 2007;11:727-759. vii-viii. 17981227.
25. Lee PI, Chang MH, Lee CY, Hsu HY, Chen JS, Chen PJ, et al. Changes of serum hepatitis B virus DNA and aminotransferase levels during the course of chronic hepatitis B virus infection in children. Hepatology 1990;12:657-660. 2210669.
26. Lok AS, Lai CL. Acute exacerbations in Chinese patients with chronic hepatitis B virus (HBV) infection : incidence, predisposing factors and etiology. J hepatol 1990;10:29-34. 2307827.
27. McMahon BJ, Holck P, Bulkow L, Snowball M. Serologic and clinical outcomes of 1536 Alaska Natives chronically infected with hepatitis B virus. Ann Intern Med 2001;135:759-768. 11694101.
29. Hsu YS, Chien RN, Yeh CT, Sheen IS, Chiou HY, Chu CM, et al. Long-term outcome after spontaneous HBeAg seroconversion in patients with chronic hepatitis B. Hepatology 2002;35:1522-1527. 12029639.
30. Bortolotti F, Guido M, Bartolacci S, Cadrobbi P, Crivellaro C, Noventa F, et al. Chronic hepatitis B in children after e antigen seroclearance: final report of a 29-year longitudinal study. Hepatology 2006;43:556-562. 16496323.
31. Yim HJ, Lok AS. Natural history of chronic hepatitis B virus infection: what we knew in 1981 and what we know in 2005. Hepatology 2006;43(2 Suppl 1):S173-S181. 16447285.
32. Lok AS, Lai CL, Wu PC, Leung EK, Lam TS. Spontaneous hepatitis B e antigen to antibody seroconversion and reversion in Chinese patients with chronic hepatitis B virus infection. Gastroenterology 1987;92:1839-1843. 3569757.
33. Martinot-Peignoux M, Boyer N, Colombat M, Akremi R, Pham BN, Ollivier S, et al. Serum hepatitis B virus DNA levels and liver histology in inactive HBsAg carriers. J hepatol 2002;36:543-546. 11943427.
34. Zacharakis GH, Koskinas J, Kotsiou S, Papoutselis M, Tzara F, Vafeiadis N, et al. Natural history of chronic HBV infection: a cohort study with up to 12 years follow-up in North Greece (part of the Interreg I-II/EC-project). J Med Virol 2005;77:173-179. 16121378.
35. de Franchis R, Meucci G, Vecchi M, Tatarella M, Colombo M, Del Ninno E, et al. The natural history of asymptomatic hepatitis B surface antigen carriers. Ann Intern Med 1993;118:191-194. 8417636.
36. Chen YC, Sheen IS, Chu CM, Liaw YF. Prognosis following spontaneous HBsAg seroclearance in chronic hepatitis B patients with or without concurrent infection. Gastroenterology 2002;123:1084-1089. 12360470.
37. Lok AS, McMahon BJ. Chronic hepatitis B: update 2009. Hepatology 2009;50:661-662. 19714720.
38. Funk ML, Rosenberg DM, Lok AS. World-wide epidemiology of HBeAg-negative chronic hepatitis B and associated precore and core promoter variants. J Viral Hepat 2002;9:52-61. 11851903.
40. Okamoto H, Tsuda F, Akahane Y, Sugai Y, Yoshiba M, Moriyama K, et al. Hepatitis B virus with mutations in the core promoter for an e antigen-negative phenotype in carriers with antibody to e antigen. J Virol 1994;68:8102-8110. 7966600.
41. Yoo BC, Park JW, Kim HJ, Lee DH, Cha YJ, Park SM. Precore and core promoter mutations of hepatitis B virus and hepatitis B e antigen-negative chronic hepatitis B in Korea. J Hepatol 2003;38:98-103. 12480566.
42. Raimondo G, Allain JP, Brunetto MR, Buendia MA, Chen DS, Colombo M, et al. Statements from the Taormina expert meeting on occult hepatitis B virus infection. J Hepatol 2008;49:652-657. 18715666.
43. Hadziyannis SJ, Vassilopoulos D. Hepatitis B e antigen-negative chronic hepatitis B. Hepatology 2001;34:617-624. 11584355.
44. Chu CM, Liaw YF. HBsAg seroclearance in asymptomatic carriers of high endemic areas: appreciably high rates during a long-term follow-up. Hepatology 2007;45:1187-1192. 17465003.
45. Liu J, Yang HI, Lee MH, Lu SN, Jen CL, Wang LY, et al. Incidence and determinants of spontaneous hepatitis B surface antigen seroclearance: a community-based follow-up study. Gastroenterology 2010;139:474-482. 20434450.
47. Liaw YF, Sheen IS, Chen TJ, Chu CM, Pao CC. Incidence, determinants and significance of delayed clearance of serum HBsAg in chronic hepatitis B virus infection: a prospective study. Hepatology 1991;13:627-631. 2010157.
49. Ahn SH, Park YN, Park JY, Chang HY, Lee JM, Shin JE, et al. Long-term clinical and histological outcomes in patients with spontaneous hepatitis B surface antigen seroclearance. J Hepatol 2005;42:188-194. 15664243.
50. Simonetti J, Bulkow L, McMahon BJ, Homan C, Snowball M, Negus S, et al. Clearance of hepatitis B surface antigen and risk of hepatocellular carcinoma in a cohort chronically infected with hepatitis B virus. Hepatology 2010;51:1531-1537. 20087968.
51. Huo TI, Wu JC, Lee PC, Chau GY, Lui WY, Tsay SH, et al. Seroclearance of hepatitis B surface antigen in chronic carriers does not necessarily imply a good prognosis. Hepatology 1998;28:231-236. 9657117.
52. Yuen MF, Wong DK, Fung J, Ip P, But D, Hung I, et al. HBsAg Seroclearance in chronic hepatitis B in Asian patients: replicative level and risk of hepatocellular carcinoma. Gastroenterology 2008;135:1192-1199. 18722377.
53. Fattovich G, Pantalena M, Zagni I, Realdi G, Schalm SW, Christensen E, et al. Effect of hepatitis B and C virus infections on the natural history of compensated cirrhosis: a cohort study of 297 patients. Am J Gastroenterol 2002;97:2886-2895. 12425564.
54. Niederau C, Heintges T, Lange S, Goldmann G, Niederau CM, Mohr L, et al. Long-term follow-up of HBeAg-positive patients treated with interferon alfa for chronic hepatitis B. N Engl J Med 1996;334:1422-1427. 8618580.
55. Kim CY, Kim JW, Lee HS, Yoon YB, Song IS. Natural history and survival rate of chronic liver diseases in Korea: 20 years prospective analysis. Korean J Med 1994;46:168-180.
56. Lee KJ, Han KH, Chun JY, Moon YM, Lee SI, Park IS, et al. Natural history of chronic hepatitis type B throughout long-term follow-up. Korean J Gastroenterol 1997;29:343-351.
57. McMahon BJ. Natural history of chronic hepatitis B. Clin Liver Dis 2010;14:381-396. 20638020.
58. Beasley RP. Hepatitis B virus. The major etiology of hepatocellular carcinoma. Cancer 1988;61:1942-1956. 2834034.
59. Goldstein ST, Zhou F, Hadler SC, Bell BP, Mast EE, Margolis HS. A mathematical model to estimate global hepatitis B disease burden and vaccination impact. Int J Epidemiol 2005;34:1329-1339. 16249217.
60. McMahon BJ, Bulkow L, Harpster A, Snowball M, Lanier A, Sacco F, et al. Screening for hepatocellular carcinoma in Alaska natives infected with chronic hepatitis B: a 16-year population-based study. Hepatology 2000;32:842-846. 11003632.
61. Alberts SR, Lanier AP, McMahon BJ, Harpster A, Bulkow LR, Heyward WL, et al. Clustering of hepatocellular carcinoma in Alaska Native families. Genet Epidemiol 1991;8:127-139. 1655562.
62. Hainaut P, Boyle P. Curbing the liver cancer epidemic in Africa. Lancet 2008;371:367-368. 18242399.
63. Chen ZM, Liu BQ, Boreham J, Wu YP, Chen JS, Peto R. Smoking and liver cancer in China: case-control comparison of 36,000 liver cancer deaths vs. 17,000 cirrhosis deaths. Int J Cancer 2003;107:106-112. 12925964.
64. Wang CS, Yao WJ, Chang TT, Wang ST, Chou P. The impact of type 2 diabetes on the development of hepatocellular carcinoma in different viral hepatitis statuses. Cancer Epidemiol Biomarkers Prev 2009;18:2054-2060. 19549812.
65. Peng D, Han Y, Ding H, Wei L. Hepatic steatosis in chronic hepatitis B patients is associated with metabolic factors more than viral factors. J Gastroenterol Hepatol 2008;23:1082-1088. 18707599.
66. Yun JW, Cho YK, Park JH, Kim HJ, Park DI, Sohn CI, et al. Hepatic steatosis and fibrosis in young men with treatment-naive chronic hepatitis B. Liver Int 2009;29:878-883. 19192167.
67. Minakari M, Molaei M, Shalmani HM, Alizadeh AH, Jazi AH, Naderi N, et al. Liver steatosis in patients with chronic hepatitis B infection: host and viral risk factors. Eur J Gastroenterol Hepatol 2009;21:512-516. 19190500.
69. La Vecchia C. Coffee, liver enzymes, cirrhosis and liver cancer. J Hepatol 2005;42:444-446. 15763323.
70. Tanaka K, Hara M, Sakamoto T, Higaki Y, Mizuta T, Eguchi Y, et al. Inverse association between coffee drinking and the risk of hepatocellular carcinoma: a case-control study in Japan. Cancer Sci 2007;98:214-218. 17233838.
71. Cadden IS, Partovi N, Yoshida EM. Review article: possible beneficial effects of coffee on liver disease and function. Aliment Pharmacol Ther 2007;26:1-8. 17555416.
72. Masterton GS, Hayes PC. Coffee and the liver: a potential treatment for liver disease? Eur J Gastroenterol Hepatol 2010;22:1277-1283. 20802342.
73. Harris RA, Chen G, Lin WY, Shen FM, London WT, Evans AA. Spontaneous clearance of high-titer serum HBV DNA and risk of hepatocellular carcinoma in a Chinese population. Cancer Causes Control 2003;14:995-1000. 14750539.
74. Chen CJ, Yang HI, Su J, Jen CL, You SL, Lu SN, et al. Risk of hepatocellular carcinoma across a biological gradient of serum hepatitis B virus DNA level. JAMA 2006;295:65-73. 16391218.
75. Yang HI, Lu SN, Liaw YF, You SL, Sun CA, Wang LY, et al. Hepatitis B e antigen and the risk of hepatocellular carcinoma. N Engl J Med 2002;347:168-174. 12124405.
76. Iloeje UH, Yang HI, Su J, Jen CL, You SL, Chen CJ. Predicting cirrhosis risk based on the level of circulating hepatitis B viral load. Gastroenterology 2006;130:678-686. 16530509.
77. Yu MW, Yeh SH, Chen PJ, Liaw YF, Lin CL, Liu CJ, et al. Hepatitis B virus genotype and DNA level and hepatocellular carcinoma: a prospective study in men. J Natl Cancer Inst 2005;97:265-272. 15713961.
79. Chu CJ, Keeffe EB, Han SH, Perrillo RP, Min AD, Soldevila-Pico C, et al. Hepatitis B virus genotypes in the United States: results of a nationwide study. Gastroenterology 2003;125:444-451. 12891547.
80. Kim JK, Chang HY, Lee JM, Baatarkhuu O, Yoon YJ, Park JY, et al. Specific mutations in the enhancer II/core promoter/precore regions of hepatitis B virus subgenotype C2 in Korean patients with hepatocellular carcinoma. J Med Virol 2009;81:1002-1008. 19382267.
81. Choi JW, Ahn SH, Park JY, Chang HY, Kim JK, Baatarkhuu O, et al. Hepatitis B e antigen-negative mutations in the precore and core promoter regions in Korean patients. J Med Virol 2009;81:594-601. 19235871.
83. Grandjacques C, Pradat P, Stuyver L, Chevallier M, Chevallier P, Pichoud C, et al. Rapid detection of genotypes and mutations in the pre-core promoter and the pre-core region of hepatitis B virus genome: correlation with viral persistence and disease severity. J Hepatol 2000;33:430-439. 11019999.
84. Naoumov NV, Schneider R, Grötzinger T, Jung MC, Miska S, Pape GR, et al. Precore mutant hepatitis B virus infection and liver disease. Gastroenterology 1992;102:538-543. 1732124.
85. Ohnishi K, Terabayashi H, Unuma T, Takahashi A, Okuda K. Effects of habitual alcohol intake and cigarette smoking on the development of hepatocellular carcinoma. Alcohol Clin Exp Res 1987;11:45-48. 3032014.
86. Chevillotte G, Durbec JP, Gerolami A, Berthezene P, Bidart JM, Camatte R. Interaction between hepatitis b virus and alcohol consumption in liver cirrhosis. An epidemiologic study. Gastroenterology 1983;85:141-145. 6852447.
87. Villa E, Rubbiani L, Barchi T, Ferretti I, Grisendi A, De Palma M, et al. Susceptibility of chronic symptomless HBsAg carriers to ethanol-induced hepatic damage. Lancet 1982;2:1243-1244. 6128548.
88. Morgan TR, Mandayam S, Jamal MM. Alcohol and hepatocellular carcinoma. Gastroenterology 2004;127(5 Suppl 1):S87-S96. 15508108.
89. Donato F, Tagger A, Gelatti U, Parrinello G, Boffetta P, Albertini A, et al. Alcohol and hepatocellular carcinoma: the effect of lifetime intake and hepatitis virus infections in men and women. Am J Epidemiol 2002;155:323-331. 11836196.
91. Becker U, Deis A, Sørensen TI, Grønbaek M, Borch-Johnsen K, Müller CF, et al. Prediction of risk of liver disease by alcohol intake, sex, and age: a prospective population study. Hepatology 1996;23:1025-1029. 8621128.
92. Loomba R, Yang HI, Su J, Brenner D, Iloeje U, Chen CJ. Obesity and alcohol synergize to increase the risk of incident hepatocellular carcinoma in men. Clin Gastroenterol Hepatol 2010;8:891-898. 898.e1-898.e2. 20621202.
93. Mast EE, Weinbaum CM, Fiore AE, Alter MJ, Bell BP, Finelli L, et al. A comprehensive immunization strategy to eliminate transmission of hepatitis B virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP) Part II: immunization of adults. MMWR Recomm Rep 2006;55:1-33 quiz CE1-4. 17159833.
94. Mast EE, Margolis HS, Fiore AE, Brink EW, Goldstein ST, Wang SA, et al. A comprehensive immunization strategy to eliminate transmission of hepatitis B virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP) part 1: immunization of infants, children, and adolescents. MMWR Recomm Rep 2005;54:1-31. 16371945.
95. Beasley RP, Hwang LY, Lee GC, Lan CC, Roan CH, Huang FY, et al. Prevention of perinatally transmitted hepatitis B virus infections with hepatitis B virus infections with hepatitis B immune globulin and hepatitis B vaccine. Lancet 1983;2:1099-1102. 6138642.
96. Hill JB, Sheffield JS, Kim MJ, Alexander JM, Sercely B, Wendel GD. Risk of hepatitis B transmission in breast-fed infants of chronic hepatitis B carriers. Obstet Gynecol 2002;99:1049-1052. 12052598.
97. Nordenfelt E, Dahlquist E. HBsAg positive adopted children as a cause of intrafamilial spread of hepatitis B. Scand J Infect Dis 1978;10:161-163. 715381.
98. Steinberg SC, Alter HJ, Leventhal BG. The risk of hepatitis transmission to family contacts of leukemia patients. J Pediatr 1975;87:753-756. 1185341.
99. U.S. Public Health Service. Updated U.S. Public Health Service Guidelines for the Management of Occupational Exposures to HBV, HCV, and HIV and Recommendations for Postexposure Prophylaxis. MMWR Recomm Rep 2001;50:1-52.
100. Keeffe EB. Hepatitis A and B superimposed on chronic liver disease: vaccine-preventable diseases. Trans Am Clin Climatol Assoc 2006;117:227-237. 18528476.
101. Craig AS, Schaffner W. Prevention of hepatitis A with the hepatitis A vaccine. N Engl J Med 2004;350:476-481. 14749456.
102. Lemon SM, Gates NL, Simms TE, Bancroft WH. IgM antibody to hepatitis B core antigen as a diagnostic parameter of acute infection with hepatitis B virus. J Infect Dis 1981;143:803-809. 6788859.
103. van Ditzhuijsen TJ, Selten GC, van Loon AM, Wolters G, Matthyssen L, Yap SH. Detection of hepatitis B virus DNA in serum and relation with the IgM class anti-HBc titers in hepatitis B virus infection. J Med Virol 1985;15:49-56. 3968544.
104. Lai CL, Lau JY, Yeoh EK, Chang WK, Lin HJ. Significance of isolated anti-HBc seropositivity by ELISA: implications and the role of radioimmunoassay. J Med Virol 1992;36:180-183. 1532979.
105. Sánchez-Quijano A, Jauregui JI, Leal M, Pineda JA, Castilla A, Abad MA, et al. Hepatitis B virus occult infection in subjects with persistent isolated anti-HBc reactivity. J Hepatol 1993;17:288-293. 8315257.
106. Raimondo G, Navarra G, Mondello S, Costantino L, Colloredo G, Cucinotta E, et al. Occult hepatitis B virus in liver tissue of individuals without hepatic disease. J Hepatol 2008;48:743-746. 18314221.
108. Karayiannis P, Fowler MJ, Lok AS, Greenfield C, Monjardino J, Thomas HC. Detection of serum HBV-DNA by molecular hybridisation. Correlation with HBeAg/anti-HBe status, racial origin, liver histology and hepatocellular carcinoma. J Hepatol 1985;1:99-106. 2997321.
109. Yuen MF, Tanaka Y, Fong DY, Fung J, Wong DK, Yuen JC, et al. Independent risk factors and predictive score for the development of hepatocellular carcinoma in chronic hepatitis B. J Hepatol 2009;50:80-88. 18977053.
110. Hong WS, Kim CY. Seroepidemiology of type A and type B hepatitis in Seoul area. Korean J Med 1982;25:19-26.
111. Song YB, Lee JH, Choi MS, Koh KC, Paik SW, Yoo BC, et al. The age-specific seroprevalence of hepatitis A virus antibody in Korea. Korean J Hepatol 2007;13:27-33. 17380072.
112. Yun SW, Lee WK, Cho SY, Moon SH, Shin HD, Yun SY, et al. The Seroprevalence Rate, Vaccination Rate and Seroconversion Rate of Hepatitis A in Central Region of Korea. Korean J Gastroenterol 2011;57:166-172. 21519164.
117. Pawlotsky JM. Hepatitis B virus (HBV) DNA assays (methods and practical use) and viral kinetics. J Hepatol 2003;39(Suppl 1):S31-S35. 14708675.
119. Chu CM, Liaw YF. Genotype C hepatitis B virus infection is associated with a higher risk of reactivation of hepatitis B and progression to cirrhosis than genotype B: a longitudinal study of hepatitis B e antigen-positive patients with normal aminotransferase levels at baseline. J Hepatol 2005;43:411-417. 16006001.
120. Sumi H, Yokosuka O, Seki N, Arai M, Imazeki F, Kurihara T, et al. Influence of hepatitis B virus genotypes on the progression of chronic type B liver disease. Hepatology 2003;37:19-26. 12500184.
121. Yu MW, Yeh SH, Chen PJ, Liaw YF, Lin CL, Liu CJ, et al. Hepatitis B virus genotype and DNA level and hepatocellular carcinoma: a prospective study in men. J Natl Cancer Inst 2005;97:265-272. 15713961.
122. Chu CM, Liaw YF. Predictive factors for reactivation of hepatitis B following hepatitis B e antigen seroconversion in chronic hepatitis B. Gastroenterology 2007;133:1458-1465. 17935720.
124. Kao JH, Chen DS. Clinical relevance of hepatitis B virus genotypes Ba and Bj in Taiwan. Gastroenterology 2003;125:1916-1917 author reply 1917-1918. 14727634.
125. Kao JH, Wu NH, Chen PJ, Lai MY, Chen DS. Hepatitis B genotypes and the response to interferon therapy. J Hepatol 2000;33:998-1002. 11131465.
126. Keeffe EB, Dieterich DT, Han SH, Jacobson IM, Martin P, Schiff ER, et al. A treatment algorithm for the management of chronic hepatitis B virus infection in the United States: 2008 update. Clin Gastroenterol Hepatol 2008;6:1315-1341. 18845489.
127. Perrillo RP, Lai CL, Liaw YF, Dienstag JL, Schiff ER, Schalm SW, et al. Predictors of HBeAg loss after lamivudine treatment for chronic hepatitis B. Hepatology 2002;36:186-194. 12085364.
128. Prati D, Taioli E, Zanella A, Della Torre E, Butelli S, Del Vecchio E, et al. Updated definitions of healthy ranges for serum alanine aminotransferase levels. Ann Intern Med 2002;137:1-10. 12093239.
129. Kariv R, Leshno M, Beth-Or A, Strul H, Blendis L, Kokia E, et al. Re-evaluation of serum alanine aminotransferase upper normal limit and its modulating factors in a large-scale population study. Liver Int 2006;26:445-450. 16629648.
130. Kim HC, Nam CM, Jee SH, Han KH, Oh DK, Suh I. Normal serum aminotransferase concentration and risk of mortality from liver diseases: prospective cohort study. BMJ 2004;328:983. 15028636.
132. Lai M, Hyatt BJ, Nasser I, Curry M, Afdhal NH. The clinical significance of persistently normal ALT in chronic hepatitis B infection. J Hepatol 2007;47:760-767. 17928090.
133. Korean Liver Cancer Study Group and National Cancer Center, Korea. Practice guidelines for management of hepatocellular carcinoma 2009. Korean J Hepatol 2009;15:391-423. 19783891.
134. Liaw YF, Sung JJ, Chow WC, Farrell G, Lee CZ, Yuen H, et al. Lamivudine for patients with chronic hepatitis B and advanced liver disease. N Engl J Med 2004;351:1521-1531. 15470215.
135. Shim JH, Lee HC, Kim KM, Lim YS, Chung YH, Lee YS, et al. Efficacy of entecavir in treatment-naive patients with hepatitis B virus-related decompensated cirrhosis. J Hepatol 2010;52:176-182. 20006394.
136. Liaw YF, Sheen IS, Lee CM, Akarca US, Papatheodoridis GV, Suet-Hing Wong F, et al. Tenofovir disoproxil fumarate (TDF), emtricitabine/TDF, and entecavir in patients with decompensated chronic hepatitis B liver disease. Hepatology 2011;53:62-72. 21254162.
137. Matsumoto A, Tanaka E, Rokuhara A, Kiyosawa K, Kumada H, Omata M, et al. Efficacy of lamivudine for preventing hepatocellular carcinoma in chronic hepatitis B: A multicenter retrospective study of 2795 patients. Hepatol Res 2005;32:173-184. 16024289.
138. Yuen MF, Seto WK, Chow DH, Tsui K, Wong DK, Ngai VW, et al. Long-term lamivudine therapy reduces the risk of long-term complications of chronic hepatitis B infection even in patients without advanced disease. Antivir Ther 2007;12:1295-1303. 18240869.
139. Wong GL, Wong VW, Choi PC, Chan AW, Chim AM, Yiu KK, et al. Evaluation of alanine transaminase and hepatitis B virus DNA to predict liver cirrhosis in hepatitis B e antigen-negative chronic hepatitis B using transient elastography. Am J Gastroenterol 2008;103:3071-3081. 19086958.
140. Ishiguro S, Inoue M, Tanaka Y, Mizokami M, Iwasaki M, Tsugane S. Serum aminotransferase level and the risk of hepatocellular carcinoma: a population-based cohort study in Japan. Eur J Cancer Prev 2009;18:26-32. 19077561.
141. Regev A, Berho M, Jeffers LJ, Milikowski C, Molina EG, Pyrsopoulos NT, et al. Sampling error and intraobserver variation in liver biopsy in patients with chronic HCV infection. Am J Gastroenterol 2002;97:2614-2618. 12385448.
142. Bedossa P, Dargere D, Paradis V. Sampling variability of liver fibrosis in chronic hepatitis C. Hepatology 2003;38:1449-1457. 14647056.
143. Chu CM, Hung SJ, Lin J, Tai DI, Liaw YF. Natural history of hepatitis B e antigen to antibody seroconversion in patients with normal serum aminotransferase levels. Am J Med 2004;116:829-834. 15178498.
144. Lin SM, Yu ML, Lee CM, Chien RN, Sheen IS, Chu CM, et al. Interferon therapy in HBeAg positive chronic hepatitis reduces progression to cirrhosis and hepatocellular carcinoma. J Hepatol 2007;46:45-52. 17107734.
145. Mommeja-Marin H, Mondou E, Blum MR, Rousseau F. Serum HBV DNA as a marker of efficacy during therapy for chronic HBV infection: analysis and review of the literature. Hepatology 2003;37:1309-1319. 12774009.
146. Schiff ER, Lee SS, Chao YC, Kew Yoon S, Bessone F, Wu SS, et al. Long-term treatment with entecavir induces reversal of advanced fibrosis or cirrhosis in patients with chronic hepatitis B. Clin Gastroenterol Hepatol 2011;9:274-276. 21145419.
147. Yuan HJ, Yuen MF, Ka-Ho Wong D, Sablon E, Lai CL. The relationship between HBV-DNA levels and cirrhosis-related complications in Chinese with chronic hepatitis B. J Viral Hepat 2005;12:373-379. 15985007.
148. Liaw YF, Brunetto MR, Hadziyannis S. The natural history of chronic HBV infection and geographical differences. Antivir Ther 2010;15(Suppl 3):25-33. 21041901.
149. Fattovich G, Giustina G, Sanchez-Tapias J, Quero C, Mas A, Olivotto PG, et al. Delayed clearan ce of serum HBsAg in compensated cirrhosis B: relation to interferon alpha therapy and disease prognosis. European Concerted Action on Viral Hepatitis (EUROHEP). Am J Gastroenterol 1998;93:896-900. 9647014.
150. van Zonneveld M, Honkoop P, Hansen BE, Niesters HG, Darwish Murad S, de Man RA, et al. Long-term follow-up of alpha-interferon treatment of patients with chronic hepatitis B. Hepatology 2004;39:804-810. 14999700.
151. Lampertico P, Del Ninno E, Viganò M, Romeo R, Donato MF, Sablon E, et al. Long-term suppression of hepatitis B e antigen-negative chronic hepatitis B by 24-month interferon therapy. Hepatology 2003;37:756-763. 12668967.
152. Gish RG, Lok AS, Chang TT, de Man RA, Gadano A, Sollano J, et al. Entecavir therapy for up to 96 weeks in patients with HBeAg-positive chronic hepatitis B. Gastroenterology 2007;133:1437-1444. 17983800.
153. Jung YK, Kim JH, Lee YS, Lee HJ, Yoon E, Jung ES, et al. Change in serum hepatitis B surface antigen level and its clinical significance in treatment-naive, hepatitis B e antigen-positive patients receiving entecavir. J Clin Gastroenterol 2010;44:653-657. 20216430.
154. Brunetto MR, Moriconi F, Bonino F, Lau GK, Farci P, Yurdaydin C, et al. Hepatitis B virus surface antigen levels: a guide to sustained response to peginterferon alfa-2a in HBeAg-negative chronic hepatitis B. Hepatology 2009;49:1141-1150. 19338056.
155. Hadziyannis SJ, Tassopoulos NC, Heathcote EJ, Chang TT, Kitis G, Rizzetto M, et al. Long-term therapy with adefovir dipivoxil for HBeAg-negative chronic hepatitis B. N Engl J Med 2005;352:2673-2681. 15987916.
156. Liu F, Wang L, Li XY, Liu YD, Wang JB, Zhang ZH, et al. Poor durability of lamivudine effectiveness despite stringent cessation criteria: A prospective clinical study in hepatitis B e antigen-negative chronic hepatitis B patients. J Gastroenterol Hepatol 2011;26:456-460. 21332542.
157. Fung J, Lai CL, Tanaka Y, Mizokami M, Yuen J, Wong DK, et al. The duration of lamivudine therapy for chronic hepatitis B: cessation vs. continuation of treatment after HBeAg seroconversion. Am J Gastroenterol 2009;104:1940-1946 quiz 1947. 19455108.
158. Lee HW, Lee HJ, Hwang JS, Sohn JH, Jang JY, Han KJ, et al. Lamivudine maintenance beyond one year after HBeAg seroconversion is a major factor for sustained virologic response in HBeAg-positive chronic hepatitis B. Hepatology 2010;51:415-421. 19902424.
159. Chang TT, Lai CL, Kew Yoon S, Lee SS, Coelho HS, Carrilho FJ, et al. Entecavir treatment for up to 5 years in patients with hepatitis B e antigen-positive chronic hepatitis B. Hepatology 2010;51:422-430. 20049753.
160. Leung NW, Lai CL, Chang TT, Guan R, Lee CM, Ng KY, et al. Extended lamivudine treatment in patients with chronic hepatitis B enhances hepatitis B e antigen seroconversion rates: results after 3 years of therapy. Hepatology 2001;33:1527-1532. 11391543.
161. Shamliyan TA, MacDonald R, Shaukat A, Taylor BC, Yuan JM, Johnson JR, et al. Antiviral therapy for adults with chronic hepatitis B: a systematic review for a National Institutes of Health Consensus Development Conference. Ann Intern Med 2009;150:111-124. 19124812.
162. Marcellin P, Chang TT, Lim SG, Tong MJ, Sievert W, Shiffman ML, et al. Adefovir dipivoxil for the treatment of hepatitis B e antigen-positive chronic hepatitis B. N Engl J Med 2003;348:808-816. 12606735.
163. Chang TT, Gish RG, de Man R, Gadano A, Sollano J, Chao YC, et al. A comparison of entecavir and lamivudine for HBeAg-positive chronic hepatitis B. N Engl J Med 2006;354:1001-1010. 16525137.
164. Chang TT, Liaw YF, Wu SS, Schiff E, Han KH, Lai CL, et al. Long-term entecavir therapy results in the reversal of fibrosis/cirrhosis and continued histological improvement in patients with chronic hepatitis B. Hepatology 2010;52:886-893. 20683932.
165. Hadziyannis SJ, Tassopoulos NC, Heathcote EJ, Chang TT, Kitis G, Rizzetto M, et al. Long-term therapy with adefovir dipivoxil for HBeAg-negative chronic hepatitis B for up to 5 years. Gastroenterology 2006;131:1743-1751. 17087951.
166. Lai CL, Shouval D, Lok AS, Chang TT, Cheinquer H, Goodman Z, et al. Entecavir versus lamivudine for patients with HBeAg-negative chronic hepatitis B. N Engl J Med 2006;354:1011-1020. 16525138.
168. Andreani T, Serfaty L, Mohand D, Dernaika S, Wendum D, Chazouillères O, et al. Chronic hepatitis B virus carriers in the immunotolerant phase of infection: histologic findings and outcome. Clin Gastroenterol Hepatol 2007;5:636-641. 17428739.
169. Lee KS, Kim DJ. Korean Association for the Study of the Liver Guideline Committee. Management of Chronic Hepatitis B. Korean J Hepatol 2007;13:447-488. 19054901.
172. Dong MH, Bettencourt R, Barrett-Connor E, Loomba R. Alanine aminotransferase decreases with age: the Rancho Bernardo Study. PLoS One 2010;5:e14254. 21170382.
173. Park JY, Park YN, Kim DY, Paik YH, Lee KS, Moon BS, et al. High prevalence of significant histology in asymptomatic chronic hepatitis B patients with genotype C and high serum HBV DNA levels. J Viral Hepat 2008 6 19;[Epub ahead of print].
174. Kumar M, Sarin SK, Hissar S, Pande C, Sakhuja P, Sharma BC, et al. Virologic and histologic features of chronic hepatitis B virus-infected asymptomatic patients with persistently normal ALT. Gastroenterology 2008;134:1376-1384. 18471514.
175. Tong MJ, Hsien C, Hsu L, Sun HE, Blatt LM. Treatment recommendations for chronic hepatitis B: an evaluation of current guidelines based on a natural history study in the United States. Hepatology 2008;48:1070-1078. 18688879.
176. Tong MJ, Hsu L, Chang PW, Blatt LM. Evaluation of current treatment recommendations for chronic hepatitis B: a 2011 update. J Gastroenterol Hepatol 2011;26:829-835. 21214888.
177. Tsang PS, Trinh H, Garcia RT, Phan JT, Ha NB, Nguyen H, et al. Significant prevalence of histologic disease in patients with chronic hepatitis B and mildly elevated serum alanine aminotransferase levels. Clin Gastroenterol Hepatol 2008;6:569-574. 18455697.
178. Chu CJ, Hussain M, Lok AS. Quantitative serum HBV DNA levels during different stages of chronic hepatitis B infection. Hepatology 2002;36:1408-1415. 12447866.
179. Papatheodoridis GV, Dimou E, Dimakopoulos K, Manolakopoulos S, Rapti I, Kitis G, et al. Outcome of hepatitis B e antigen-negative chronic hepatitis B on long-term nucleos(t)ide analog therapy starting with lamivudine. Hepatology 2005;42:121-129. 15962291.
180. Eun JR, Lee HJ, Kim TN, Lee KS. Risk assessment for the development of hepatocellular carcinoma: according to on-treatment viral response during long-term lamivudine therapy in hepatitis B virus-related liver disease. J Hepatol 2010;53:118-125. 20471129.
181. Sung JJ, Tsoi KK, Wong VW, Li KC, Chan HL. Meta-analysis: Treatment of hepatitis B infection reduces risk of hepatocellular carcinoma. Aliment Pharmacol Ther 2008;28:1067-1077. 18657133.
182. Yao FY, Terrault NA, Freise C, Maslow L, Bass NM. Lamivudine treatment is beneficial in patients with severely decompensated cirrhosis and actively replicating hepatitis B infection awaiting liver transplantation: a comparative study using a matched, untreated cohort. Hepatology 2001;34:411-416. 11481627.
183. Consensus statements on the prevention and management of hepatitis B and hepatitis C in the Asia-Pacific region. Core Working Party for Asia-Pacific Consensus on Hepatitis B and C. J Gastroenterol Hepatol 2000;15:825-841. 11022822.
184. Lok AS, McMahon BJ. Chronic hepatitis B. Hepatology 2001;34:1225-1241. 11732013.
185. Lok AS, Heathcote EJ, Hoofnagle JH. Management of hepatitis B: 2000--summary of a workshop. Gastroenterology 2001;120:1828-1853. 11375963.
186. Rockey DC, Caldwell SH, Goodman ZD, Nelson RC, Smith AD. Liver biopsy. Hepatology 2009;49:1017-1044. 19243014.
187. Zeuzem S, Gane E, Liaw YF, Lim SG, DiBisceglie A, Buti M, et al. Baseline characteristics and early on-treatment response predict the outcomes of 2 years of telbivudine treatment of chronic hepatitis B. J Hepatol 2009;51:11-20. 19345439.
188. Dienstag JL, Goldin RD, Heathcote EJ, Hann HW, Woessner M, Stephenson SL, et al. Histological outcome during long-term lamivudine therapy. Gastroenterology 2003;124:105-117. 12512035.
189. Tariq M, Jafri W, Ansari T, Awan S, Ali F, Shah M, et al. Medical mortality in Pakistan: experience at a tertiary care hospital. Postgrad Med J 2009;85:470-474. 19734514.
190. Fattovich G, Giustina G, Realdi G, Corrocher R, Schalm SW. Long-term outcome of hepatitis B e antigen-positive patients with compensated cirrhosis treated with interferon alfa. European Concerted Action on Viral Hepatitis (EUROHEP). Hepatology 1997;26:1338-1342. 9362381.
191. Peters M, Davis GL, Dooley JS, Hoofnagle JH. The interferon system in acute and chronic viral hepatitis. Prog Liver Dis 1986;8:453-467. 2424048.
192. Buster EH, Hansen BE, Buti M, Delwaide J, Niederau C, Michielsen PP, et al. Peginterferon alpha-2 b is safe and effective in HBeAg-positive chronic hepatitis B patients with advanced fibrosis. Hepatology 2007;46:388-394. 17604363.
193. Schiff E, Simsek H, Lee WM, Chao YC, Sette H Jr, Janssen HL, et al. Efficacy and safety of entecavir in patients with chronic hepatitis B and advanced hepatic fibrosis or cirrhosis. Am J Gastroenterol 2008;103:2776-2783. 18721244.
194. Liang J, Han T, Xiao SX. Telbivudine treatment on cirrhosis resulting from chronic hepatitis B. Zhonghua Gan Zang Bing Za Zhi 2009;17:24-27. 19203447.
195. Kim JH, Yim HJ, Jung ES, Jung YK, Kim JH, Seo YS, et al. Virologic and biochemical responses to clevudine in patients with chronic HBV infection-associated cirrhosis: data at week 48. J Viral Hepat 2011;18:287-293. 20367793.
196. Perrillo R, Tamburro C, Regenstein F, Balart L, Bodenheimer H, Silva M, et al. Low-dose, titratable interferon alfa in decompensated liver disease caused by chronic infection with hepatitis B virus. Gastroenterology 1995;109:908-916. 7657121.
197. Villeneuve JP, Condreay LD, Willems B, Pomier-Layrargues G, Fenyves D, Bilodeau M, et al. Lamivudine treatment for decompensated cirrhosis resulting from chronic hepatitis B. Hepatology 2000;31:207-210. 10613747.
198. Chien RN, Lin CH, Liaw YF. The effect of lamivudine therapy in hepatic decompensation during acute exacerbation of chronic hepatitis B. J Hepatol 2003;38:322-327. 12586298.
199. Fontana RJ, Hann HW, Perrillo RP, Vierling JM, Wright T, Rakela J, et al. Determinants of early mortality in patients with decompensated chronic hepatitis B treated with antiviral therapy. Gastroenterology 2002;123:719-727. 12198698.
200. Chan HLY, Hsu CW, Sarin S, Suh DJ, Piravisuth T, Ganed E, et al. Efficacy and safety of telbivudine versus lamivudine in the treatment of decompensated chronic hepatitis B for 2 years. [Abstract]. Hepatol Int 2010;4:146.
201. Moon W, Choi MS, Moon YM, Paik SW, Lee JH, Koh KC, et al. Efficacy and safety of adefovir dipivoxil in patients with decompensated liver cirrhosis with Lamivudine resistance compared to patients with compensated liver disease. Korean J Hepatol 2005;11:125-134. 15980671.
202. Liaw YF, Raptopoulou-Gigi M, Cheinquer H, Sarin SK, Tanwandee T, Leung N, et al. Efficacy and safety of entecavir versus adefovir in chronic hepatitis B patients with hepatic decompensation: a randomized, open-label study. Hepatology 2011;54:91-100. 21503940.
203. Janssen HL, van Zonneveld M, Senturk H, Zeuzem S, Akarca US, Cakaloglu Y, et al. Pegylated interferon alfa-2b alone or in combination with lamivudine for HBeAg-positive chronic hepatitis B: a randomised trial. Lancet 2005;365:123-129. 15639293.
204. Lau GK, Piratvisuth T, Luo KX, Marcellin P, Thongsawat S, Cooksley G, et al. Peginterferon Alfa-2a, lamivudine, and the combination for HBeAg-positive chronic hepatitis B. N Engl J Med 2005;352:2682-2695. 15987917.
205. Chan HL, Leung NW, Hui AY, Wong VW, Liew CT, Chim AM, et al. A randomized, controlled trial of combination therapy for chronic hepatitis B: comparing pegylated interferon-alpha2b and lamivudine with lamivudine alone. Ann Intern Med 2005;142:240-250. 15710957.
206. Marcellin P, Lau GK, Bonino F, Farci P, Hadziyannis S, Jin R, et al. Peginterferon alfa-2a alone, lamivudine alone, and the two in combination in patients with HBeAg-negative chronic hepatitis B. N Engl J Med 2004;351:1206-1217. 15371578.
208. Schiff ER, Dienstag JL, Karayalcin S, Grimm IS, Perrillo RP, Husa P, et al. Lamivudine and 24 weeks of lamivudine/interferon combination therapy for hepatitis B e antigen-positive chronic hepatitis B in interferon nonresponders. J Hepatol 2003;38:818-826. 12763376.
209. Wursthorn K, Lutgehetmann M, Dandri M, Buggisch P, Zollner B, Longerich T, et al. Peginterferon alpha-2b plus adefovir induce strong cccDNA decline and HBsAg reduction in patients with chronic hepatitis B. Hepatology 2006;44:675-684. 16941693.
210. Sung JJ, Lai JY, Zeuzem S, Chow WC, Heathcote EJ, Perrillo RP, et al. Lamivudine compared with lamivudine and adefovir dipivoxil for the treatment of HBeAg-positive chronic hepatitis B. J Hepatol 2008;48:728-735. 18329126.
211. Lai CL, Leung N, Teo EK, Tong M, Wong F, Hann HW, et al. A 1-year trial of telbivudine, lamivudine, and the combination in patients with hepatitis B e antigen-positive chronic hepatitis B. Gastroenterology 2005;129:528-536. 16083710.
212. Hui CK, Zhang HY, Bowden S, Locarnini S, Luk JM, Leung KW, et al. 96 weeks combination of adefovir dipivoxil plus emtricitabine vs. adefovir dipivoxil monotherapy in the treatment of chronic hepatitis B. J Hepatol 2008;48:714-720. 18207280.
213. Carey I, Harrison PM. Monotherapy versus combination therapy for the treatment of chronic hepatitis B. Expert Opin Investig Drugs 2009;18:1655-1666.
215. Afdhal NH, Lok AS, Di Bisceglie AM. Clinical decisions. Management of incidental hepatitis C virus infection. N Engl J Med 2009;360:1902-1906. 19403909.
217. Ahn SH, Yuen L, Revill P. Clarification required for the definition of hepatitis B virus subgenotypes C1 and C2. Intervirology 2009;52:321-322. 19776617.
219. Lee JM, Ahn SH, Kim HS, Park H, Chang HY, Kim do Y, et al. Quantitative hepatitis B surface antigen and hepatitis B e antigen titers in prediction of treatment response to entecavir. Hepatology 2011;53:1486-1493. 21520167.
220. Kim do Y, Ahn SH, Lee HW, Park JY, Kim SU, Paik YH, et al. Clinical course of virologic breakthrough after emergence of YMDD mutations in HBeAg-positive chronic hepatitis B. Intervirology 2008;51:293-298. 19001828.
221. Lee JM, Park JY, Kim do Y, Nguyen T, Hong SP, Kim SO, et al. Long-term adefovir dipivoxil monotherapy for up to 5 years in lamivudine-resistant chronic hepatitis B. Antivir Ther 2010;15:235-241. 20386079.
222. Lee JM, Kim HJ, Park JY, Lee CK, Kim do Y, Kim JK, et al. Rescue monotherapy in lamivudine-resistant hepatitis B e antigen-positive chronic hepatitis B: adefovir versus entecavir. Antivir Ther 2009;14:705-712. 19704174.
223. Kim H, Han K, Ahn SH, Kim EO, Chang HY, Moon MS, et al. Evaluation of methods for monitoring drug resistance in chronic hepatitis B patients during lamivudine therapy based on mass spectrometry and reverse hybridization. Antivir Ther 2005;10:441-449. 15918335.
224. Han KH, Hong SP, Choi SH, Shin SK, Cho SW, Ahn SH, et al. Comparison of multiplex restriction fragment mass polymorphism and sequencing analyses for detecting entecavir resistance in chronic hepatitis B. Antivir Ther 2011;16:77-87. 21311111.
225. Liaw YF, Xie Q, Han KH, Gane EJ, Piratvusuth T, McCloud PI, et al. Shorter duration and lower dose of peginterferon alpha-2a therapy results in inferior HBeAg seroconversion rates compared with the duration and dose of 48 weeks and 180ug: Neptune study. [Abstract]. Hepatology 52(Suppl 1):112A.
226. Gane E, Jia J, Han K, Tanwandee T, Chuang WL, Marcellin O, et al. Neptune study: On-treatment HBsAg level analysis confirms prediction of response observed in phase 3 study of peginterferon alpha-2a in HBeAg-positive patients. [Abstract]. J Hepatol 2011;54(Suppl 1):S31.
227. Chon YE, Kim SU, Lee CK, Heo J, Kim JK, Yoon KT, et al. Partial virological response to entecavir in treatment-naïve patients with chronic hepatitis B. Antivir Ther 2011;16:469-477. 21685534.
228. Buster EH, Hansen BE, Lau GK, Piratvisuth T, Zeuzem S, Steyerberg EW, et al. Factors that predict response of patients with hepatitis B e antigen-positive chronic hepatitis B to peginterferon-alfa. Gastroenterology 2009;137:2002-2009. 19737568.
229. Kau A, Vermehren J, Sarrazin C. Treatment predictors of a sustained virologic response in hepatitis B and C. J Hepatol 2008;49:634-651. 18715665.
230. Fried MW, Piratvisuth T, Lau GK, Marcellin P, Chow WC, Cooksley G, et al. HBeAg and hepatitis B virus DNA as outcome predictors during therapy with peginterferon alfa-2a for HBeAg-positive chronic hepatitis B. Hepatology 2008;47:428-434. 18220290.
231. Flink HJ, van Zonneveld M, Hansen BE, de Man RA, Schalm SW, Janssen HL. Treatment with Peg-interferon alpha-2b for HBeAg-positive chronic hepatitis B: HBsAg loss is associated with HBV genotype. Am J Gastroenterol 2006;101:297-303. 16454834.
232. Perrillo RP, Schiff ER, Davis GL, Bodenheimer HC Jr, Lindsay K, Payne J, et al. The Hepatitis Interventional Therapy Group. A randomized, controlled trial of interferon alfa-2b alone and after prednisone withdrawal for the treatment of chronic hepatitis B. N Engl J Med 1990;323:295-301. 2195346.
233. Lok AS, Wu PC, Lai CL, Lau JY, Leung EK, Wong LS, et al. A controlled trial of interferon with or without prednisone priming for chronic hepatitis B. Gastroenterology 1992;102:2091-2097. 1587429.
234. Zoulim F, Perrillo R. Hepatitis B: reflections on the current approach to antiviral therapy. J Hepatol 2008;48(Suppl 1):S2-S19. 18304680.
235. Lai CL, Gane E, Liaw YF, Hsu CW, Thongsawat S, Wang Y, et al. Telbivudine versus lamivudine in patients with chronic hepatitis B. N Engl J Med 2007;357:2576-2588. 18094378.
236. Yuen M, Fong DY, Wong DK, Yuen JC, Fung J, Lai C. Hepatitis B virus DNA levels at week 4 of lamivudine treatment predict the 5-year ideal response. Hepatology 2007;46:1695-1703. 18027877.
237. Zoulim F, Durantel D, Deny P. Management and prevention of drug resistance in chronic hepatitis B. Liver Int 2009;29(Suppl 1):108-115. 19207973.
239. Melegari M, Scaglioni PP, Wands JR. Hepatitis B virus mutants associated with 3TC and famciclovir administration are replication defective. Hepatology 1998;27:628-633. 9462667.
241. Richman DD. The impact of drug resistance on the effectiveness of chemotherapy for chronic hepatitis B. Hepatology 2000;32:866-867. 11003636.
242. Bartholomeusz A, Locarnini SA. Antiviral drug resistance: clinical consequences and molecular aspects. Semin Liver Dis 2006;26:162-170. 16673294.
243. Lok AS, Zoulim F, Locarnini S, Bartholomeusz A, Ghany MG, Pawlotsky JM, et al. Antiviral drug-resistant HBV: standardization of nomenclature and assays and recommendations for management. Hepatology 2007;46:254-265. 17596850.
244. Lai CL, Dienstag J, Schiff E, Leung NW, Atkins M, Hunt C, et al. Prevalence and clinical correlates of YMDD variants during lamivudine therapy for patients with chronic hepatitis B. Clin Infect Dis 2003;36:687-696. 12627352.
245. Lok AS, Lai CL, Leung N, Yao GB, Cui ZY, Schiff ER, et al. Long-term safety of lamivudine treatment in patients with chronic hepatitis B. Gastroenterology 2003;125:1714-1722. 14724824.
246. Gish RG, Trinh H, Leung N, Chan FK, Fried MW, Wright TL, et al. Safety and antiviral activity of emtricitabine (FTC) for the treatment of chronic hepatitis B infection: a two-year study. J Hepatol 2005;43:60-66. 15922478.
247. Stuyver LJ, Locarnini SA, Lok A, Richman DD, Carman WF, Dienstag JL, et al. Nomenclature for antiviral-resistant human hepatitis B virus mutations in the polymerase region. Hepatology 2001;33:751-757. 11230757.
248. Koh KH, Kang CJ, Kim DH, Choi YW, Kim MJ, Cheong JY, et al. Development of clevudine resistance after switching from lamivudine in a patient with chronic hepatitis B. Korean J Gastroenterol 2008;52:325-328. 19077481.
249. Liaw YF, Gane E, Leung N, Zeuzem S, Wang Y, Lai CL, et al. 2-Year GLOBE trial results: telbivudine Is superior to lamivudine in patients with chronic hepatitis B. Gastroenterology 2009;136:486-495. 19027013.
250. Yoon EL, Yim HJ, Lee HJ, Lee YS, Kim JH, Jung ES, et al. Comparison of Clevudine and Entecavir for Treatment-naive Patients With Chronic Hepatitis B Virus Infection: Two-Year Follow-up Data. J Clin Gastroenterol 2011;45:893-899. 21617542.
251. Locarnini S. Molecular virology and the development of resistant mutants: implications for therapy. Semin Liver Dis 2005;25(Suppl 1):9-19. 16103977.
252. Qi X, Xiong S, Yang H, Miller M, Delaney WE 4th. In vitro susceptibility of adefovir-associated hepatitis B virus polymerase mutations to other antiviral agents. Antivir Ther 2007;12:355-362. 17591025.
254. Tenney DJ, Rose RE, Baldick CJ, Pokornowski KA, Eggers BJ, Fang J, et al. Long-term monitoring shows hepatitis B virus resistance to entecavir in nucleoside-naive patients is rare through 5 years of therapy. Hepatology 2009;49:1503-1514. 19280622.
255. Villeneuve JP, Durantel D, Durantel S, Westland C, Xiong S, Brosgart CL, et al. Selection of a hepatitis B virus strain resistant to adefovir in a liver transplantation patient. J Hepatol 2003;39:1085-1089. 14642631.
256. Villet S, Pichoud C, Billioud G, Barraud L, Durantel S, Trépo C, et al. Impact of hepatitis B virus rtA181V/T mutants on hepatitis B treatment failure. J Hepatol 2008;48:747-755. 18331765.
257. Lampertico P, Vigano M, Manenti E, Iavarone M, Sablon E, Colombo M. Low resistance to adefovir combined with lamivudine: a 3-year study of 145 lamivudine-resistant hepatitis B patients. Gastroenterology 2007;133:1445-1451. 17983801.
258. Sheldon J, Camino N, Rodes B, Bartholomeusz A, Kuiper M, Tacke F, et al. Selection of hepatitis B virus polymerase mutations in HIV-coinfected patients treated with tenofovir. Antivir Ther 2005;10:727-734. 16218172.
259. Yim HJ, Hussain M, Liu Y, Wong SN, Fung SK, Lok AS. Evolution of multi-drug resistant hepatitis B virus during sequential therapy. Hepatology 2006;44:703-712. 16941700.
260. Lee YS, Suh DJ, Lim YS, Jung SW, Kim KM, Lee HC, et al. Increased risk of adefovir resistance in patients with lamivudine-resistant chronic hepatitis B after 48 weeks of adefovir dipivoxil monotherapy. Hepatology 2006;43:1385-1391. 16729316.
262. Yim HJ. Management of antiviral-resistant chronic hepatitis B virus infection. Korean J Gastroenterol 2008;51:346-359. 18604136.
263. Peters MG, Hann Hw H, Martin P, Heathcote EJ, Buggisch P, Rubin R, et al. Adefovir dipivoxil alone or in combination with lamivudine in patients with lamivudine-resistant chronic hepatitis B. Gastroenterology 2004;126:91-101. 14699491.
264. Rapti I, Dimou E, Mitsoula P, Hadziyannis SJ. Adding-on versus switching-to adefovir therapy in lamivudine-resistant HBeAg-negative chronic hepatitis B. Hepatology 2007;45:307-313. 17256746.
265. Lampertico P, Marzano A, Levrero M, Santantonio T, Di Marco V, Brunette M, et al. Adefovir and lamivudine combination therapy is superior to adefovir monotherapy for lamivudine-resistant patients with HBeAg-negative chronic hepatitis B. [Abstract]. J Hepatol 2007;46(Suppl 1):S191.
266. Gaia S, Barbon V, Smedile A, Olivero A, Carenzi S, Lagget M, et al. Lamivudine-resistant chronic hepatitis B: An observational study on adefovir in monotherapy or in combination with lamivudine. J Hepatol 2008;48:540-547. 18279995.
267. Lim YS, Lee TH, Heo NY, Shim JH, J LH, Suh DJ. Entecavir plus adefovir combination for chronic hepatitis B patients after failure of nucleos(t)ide analogue. [Abstract]. Korean J Gastroenterol 2010;56:A293.
268. Ahn SH, Kweon YO, Paik SW, Sohn JH, Lee KS, Kim DJ, et al. Telbivudine in combination with adefovir versus adefovir monotherapy in HBeAg-positive, lamivudine-resistant chronic hepatitis B. Hepatol Int 2011 10 12;[Epub ahead of print].
269. An HJ, Jang JW, Bae SH, Choi JY, Cho SH, Yoon SK, et al. Sustained low hepatitis B viral load predicts good outcome after curative resection in patients with hepatocellular carcinoma. J Gastroenterol Hepatol 2010;25:1876-1882. 21092000.
270. Yoon E, Yim HJ, Lee HJ, Lee SJ, Suh SJ, Hyun JJ, et al. The initial antiviral efficacy of telbivudine and adefovir combination therapy in patients with various settings of antiviral resistance. [Abstract]. Korean J Hepatol 2011;17(Suppl 3):S87.
271. van Bommel F, Wunsche T, Mauss S, Reinke P, Bergk A, Schürmann D, et al. Comparison of adefovir and tenofovir in the treatment of lamivudine-resistant hepatitis B virus infection. Hepatology 2004;40:1421-1425. 15565615.
272. van Bommel F, Zollner B, Sarrazin C, Spengler U, Hüppe D, Möller B, et al. Tenofovir for patients with lamivudine-resistant hepatitis B virus (HBV) infection and high HBV DNA level during adefovir therapy. Hepatology 2006;44:318-325. 16871563.
273. van Bommel F, de Man RA, Wedemeyer H, Deterding K, Petersen J, Buggisch P, et al. Long-term efficacy of tenofovir monotherapy for hepatitis B virus-monoinfected patients after failure of nucleoside/nucleotide analogues. Hepatology 2010;51:73-80. 19998272.
275. Patel N, Amarapurkar D. Tenofovir rescue therapy for patients with viral resistance to lamivudine and/or adefovir treatment. [Abstract]. Hepatol Int 2010;4(Suppl 1):161.
276. Chang TT, Gish RG, Hadziyannis SJ, Cianciara J, Rizzetto M, Schiff ER, et al. A dose-ranging study of the efficacy and tolerability of entecavir in Lamivudine-refractory chronic hepatitis B patients. Gastroenterology 2005;129:1198-1209. 16230074.
277. Sherman M, Yurdaydin C, Sollano J, Silva M, Liaw YF, Cianciara J, et al. Entecavir for treatment of lamivudine-refractory, HBeAg-positive chronic hepatitis B. Gastroenterology 2006;130:2039-2049. 16762627.
278. Ryu HJ, Lee JM, Ahn SH, Kim do Y, Lee MH, Han KH, et al. Efficacy of adefovir add-on lamivudine rescue therapy compared with switching to entecavir monotherapy in patients with lamivudine-resistant chronic hepatitis B. J Med Virol 2010;82:1835-1842. 20872709.
279. Yim HJ, Yoon E, Seo YS, Kim CW, Lee CD, Park SH, et al. Adding adefovir compared with switching to entecavir in patients with lamivudine-resistant chronic hepatitis B (ACE study) - A multicenter prospective randomized study: 2 year final results. [Abstract]. Hepatology 2011;54(Suppl 1):1060A-1061A.
280. Suh DJ, Lee HJ, Byun KS, Cho M, Kwon YO, Chon CY, et al. A multicenter. open-labe study of efficacy and safety of peginterferon alfa-2a (40KD) in Korean patients with HBeAg-positive CHB haboring lamivduine-resistant YMDD mutants. [Abstract]. Hepatology 2008;48(Suppl 1):747A.
281. Sun J, Hou JL, Xie Q, Li XH, Zhang JM, Wang YM, et al. Randomised clinical trial: efficacy of peginterferon alfa-2a in HBeAg positive chronic hepatitis B patients with lamivudine resistance. Aliment Pharmacol Ther 2011;34:424-431. 21692822.
282. Villet S, Pichoud C, Villeneuve JP, Trepo C, Zoulim F. Selection of a multiple drug-resistant hepatitis B virus strain in a liver-transplanted patient. Gastroenterology 2006;131:1253-1261. 17030194.
283. Lampertico P, Vigano M, Manenti E, Iavarone M, Lunghi G, Colombo M. Adefovir rapidly suppresses hepatitis B in HBeAg-negative patients developing genotypic resistance to lamivudine. Hepatology 2005;42:1414-1419. 16317671.
284. Gane E, Lai CL, Min A, Heathcote EJ, Poynard T, Kurdas OO, et al. Adefovir salvage therapy for telbivudine treated patients from Globe with virologic breakthrough. [Abstract]. Hepatol Int 2007;1:14A.
285. Cho EY, Yim HJ, Hwang SG, Kim JH, Seo YS, Kim JH, et al. Optimal management of clevudine resistant chronic hepatitis B; A multicenter retrospective study. [Abstract]. Korean J Hepatol 2010;16(Suppl 3):S46.
286. Patterson SJ, George J, Strasser SI, Lee AU, Sievert W, Nicoll AJ, et al. Tenofovir disoproxil fumarate rescue therapy following failure of both lamivudine and adefovir dipivoxil in chronic hepatitis B. Gut 2011;60:247-254. 21036792.
287. Tan J, Degertekin B, Wong SN, Husain M, Oberhelman K, Lok AS. Tenofovir monotherapy is effective in hepatitis B patients with antiviral treatment failure to adefovir in the absence of adefovir-resistant mutations. J Hepatol 2008;48:391-398. 18199519.
288. Fung SK, Andreone P, Han SH, Rajender Reddy K, Regev A, Keeffe EB, et al. Adefovir-resistant hepatitis B can be associated with viral rebound and hepatic decompensation. J Hepatol 2005;43:937-943. 16168522.
289. Reijnders JG, Deterding K, Petersen J, Zoulim F, Santantonio T, Buti M, et al. Antiviral effect of entecavir in chronic hepatitis B: influence of prior exposure to nucleos(t)ide analogues. J Hepatol 2010;52:493-500. 20185191.
290. Shim JH, Suh DJ, Kim KM, Lim YS, Lee HC, Chung YH, et al. Efficacy of entecavir in patients with chronic hepatitis B resistant to both lamivudine and adefovir or to lamivudine alone. Hepatology 2009;50:1064-1071. 19637288.
291. Heo NY, Lim YS, Lee HC, Chung YH, Lee YS, Suh DJ. Lamivudine plus adefovir or entecavir for patients with chronic hepatitis B resistant to lamivudine and adefovir. J Hepatol 2010;53:449-454. 20646776.
292. Petersen J, Lutgehetmann M, Zoulim F, Sterneck M, Janssen HL, Berg T, et al. Entecavir and tenofovir combination therpy in chronic hepatitis B: rescue therapy in patients with advanced fibrosis and multiple previous treatment failures. Results from an international multicenter cohort study [Abstract]. Hepatoloy 2009;50(Suppl 4):496A.
293. Villet S, Ollivet A, Pichoud C, Barraud L, Villeneuve JP, Trépo C, et al. Stepwise process for the development of entecavir resistance in a chronic hepatitis B virus infected patient. J Hepatol 2007;46:531-538. 17239478.
294. Yatsuji H, Hiraga N, Mori N, Hatakeyama T, Tsuge M, Imamura M, et al. Successful treatment of an entecavir-resistant hepatitis B virus variant. J Med Virol 2007;79:1811-1817. 17935165.
295. Kim SS, Lee DM, Jeong JY, Hong SP, Yoo WD, Kim SO, et al. Efficacy of lamivduine plus adefovir therapy or adefovir add on therapy for entecavir-resistant hepatitisn B patients. [Abstract]. Korean J Hepatol 2010;16(Suppl 3):S48.
296. Amini-Bavil-Olyaee S, Herbers U, Sheldon J, Luedde T, Trautwein C, Tacke F. The rtA194T polymerase mutation impacts viral replication and susceptibility to tenofovir in hepatitis B e antigen-positive and hepatitis B e antigen-negative hepatitis B virus strains. Hepatology 2009;49:1158-1165. 19263474.
297. Petersen J, Lutgehetmann M, Buti M, Brown A, Lampertico P, Zoulim F, et al. Treatment of multiresistant HBV patients with entecavir plus tenofovir. 2 years safety and efficacy analysis. An international multicenter cohort study. [Abstract]. J Hepatol 2011;54(Suppl 1):S299.
298. Locarnini S, Mason WS. Cellular and virological mechanisms of HBV drug resistance. J Hepatol 2006;44:422-431. 16364492.
299. Locarnini S, Omata M. Molecular virology of hepatitis B virus and the development of antiviral drug resistance. Liver Int 2006;26(Suppl 2):11-22.
300. Yuen MF, Sablon E, Hui CK, Yuan HJ, Decraemer H, Lai CL. Factors associated with hepatitis B virus DNA breakthrough in patients receiving prolonged lamivudine therapy. Hepatology 2001;34:785-791. 11584376.
301. Fukai K, Zhang KY, Imazeki F, Kurihara T, Mikata R, Yokosuka O. Association between lamivudine sensitivity and the number of substitutions in the reverse transcriptase region of the hepatitis B virus polymerase. J Viral Hepat 2007;14:661-666. 17697019.
302. Ahn SH, Park JY, Lee HJ, Tak WY, Um SH, Kim do Y, et al. Prospective Randomized Trial of Switching to Entecavir in Chronic Hepatitis B Patients with Suboptimal Virologic Response to Lamivudine: Interim Analysis at 48 Weeks. [Abstract]. Hepatology Int 2010;4:53A.
303. Keeffe EB, Zeuzem S, Koff RS, Dieterich DT, Esteban-Mur R, Gane EJ, et al. Report of an international workshop: Roadmap for management of patients receiving oral therapy for chronic hepatitis B. Clin Gastroenterol Hepatol 2007;5:890-897. 17632041.
304. Lok AS. How to diagnose and treat hepatitis B virus antiviral drug resistance in the liver transplant setting. Liver Transpl 2008;14(Suppl 2):S8-S14. 18825720.
305. Marcellin P, Heathcote EJ, Buti M, Gane E, de Man RA, Krastev Z, et al. Tenofovir disoproxil fumarate versus adefovir dipivoxil for chronic hepatitis B. N Engl J Med 2008;359:2442-2455. 19052126.
306. Snow-Lampart A, Chappell B, Curtis M, Zhu Y, Myrick F, Schawalder J, et al. No resistance to tenofovir disoproxil fumarate detected after up to 144 weeks of therapy in patients monoinfected with chronic hepatitis B virus. Hepatology 2011;53:763-773. 21374657.
307. Zoutendijk R, Reijnders JG, Brown A, Zoulim F, Mutimer D, Deterding K, et al. Entecavir treatment for chronic hepatitis B: adaptation is not needed for the majority of naïve patients with a partial virological response. Hepatology 2011;54:443-451. 21563196.
308. Yuki N, Nagaoka T, Yamashiro M, Mochizuki K, Kaneko A, Yamamoto K, et al. Long-term histologic and virologic outcomes of acute self-limited hepatitis B. Hepatology 2003;37:1172-1179. 12717399.
309. Shiffman ML. Management of acute hepatitis B. Clin Liver Dis 2010;14:75-91. 20123442.
311. Slifka MK, Matloubian M, Ahmed R. Bone marrow is a major site of long-term antibody production after acute viral infection. J Virol 1995;69:1895-1902. 7853531.
312. Kumar M, Satapathy S, Monga R, Das K, Hissar S, Pande C, et al. A randomized controlled trial of lamivudine to treat acute hepatitis B. Hepatology 2007;45:97-101. 17187417.
313. Tillmann HL, Hadem J, Leifeld L, Zachou K, Canbay A, Eisenbach C, et al. Safety and efficacy of lamivudine in patients with severe acute or fulminant hepatitis B, a multicenter experience. J Viral Hepat 2006;13:256-263. 16611192.
314. De Socio GV, Sgrelli A, Tosti A, Baldelli F. Severe acute hepatitis B treated with entecavir. Mediterr J Hematol Infect Dis 2011;3:e2011010. 21625314.
315. Christopeit M, Weber T, Abendroth J, Dollinger M, Lübbert C, Oehme A, et al. HBs seroconversion in a patient with acute hepatitis B treated with entecavir during immunosuppression against severe bronchiolitis obliterans in the course of chronic graft versus host disease. J Clin Virol 2010;48:218-219. 20403727.
316. Begini P, Cox MC, Angeletti S, Gigante E, Baccini F, Di Fonzo M, et al. Effectiveness of entecavir in the management of acute hepatitis B developing in a patient with Hodgkin's lymphoma: a case report. Scand J Infect Dis 2011;43:750-752. 21696249.
317. Demetris AJ, Jaffe R, Sheahan DG, Burnham J, Spero J, Iwatsuki S, et al. Recurrent hepatitis B in liver allograft recipients. Differentiation between viral hepatitis B and rejection. Am J Pathol 1986;125:161-172. 3535528.
318. Demetris AJ, Todo S, Van Thiel DH, Fung JJ, Iwaki Y, Sysyn G, et al. Evolution of hepatitis B virus liver disease after hepatic replacement. Practical and theoretical considerations. Am J Pathol 1990;137:667-676. 2399936.
319. Davies SE, Portmann BC, O'Grady JG, Aldis PM, Chaggar K, Alexander GJ, et al. Hepatic histological findings after transplantation for chronic hepatitis B virus infection, including a unique pattern of fibrosing cholestatic hepatitis. Hepatology 1991;13:150-157. 1988336.
320. Freeman RB, Sanchez H, Lewis WD, Sherburne B, Dzik WH, Khettry U, et al. Serologic and DNA follow-up data from HBsAg-positive patients treated with orthotopic liver transplantation. Transplantation 1991;51:793-797. 1901676.
321. Lake JR, Wright TL. Liver transplantation for patients with hepatitis B : what have we learned from our results? Hepatology 1991;13:796-799. 2010175.
322. O'Grady JG, Smith HM, Davies SE, Daniels HM, Donaldson PT, Tan KC, et al. Hepatitis B virus reinfection after orthotopic liver transplantation. Serological and clinical implications. J Hepatol 1992;14:104-111. 1737910.
323. Rizzetto M, Recchia S, Salizzoni M. Liver transplantation in carriers of the HBsAg. J Hepatol 1991;13:5-7. 1918879.
324. Todo S, Demetris AJ, Van Thiel D, Teperman L, Fung JJ, Starzl TE. Orthotopic liver transplantation for patients with hepatitis B virus-related liver disease. Hepatology 1991;13:619-626. 2010156.
325. Samuel D, Muller R, Alexander G, Fassati L, Ducot B, Benhamou JP, et al. Liver transplantation in European patients with the hepatitis B surface antigen. N Engl J Med 1993;329:1842-1847. 8247035.
326. Roche B, Feray C, Gigou M, Roque-Afonso AM, Arulnaden JL, Delvart V, et al. HBV DNA persistence 10 years after liver transplantation despite successful anti-HBS passive immunoprophylaxis. Hepatology 2003;38:86-95. 12829990.
327. Terrault NA, Zhou S, Combs C, Hahn JA, Lake JR, Roberts JP, et al. Prophylaxis in liver transplant recipients using a fixed dosing schedule of hepatitis B immunoglobulin. Hepatology 1996;24:1327-1333. 8938155.
328. McGory RW, Ishitani MB, Oliveira WM, Stevenson WC, McCullough CS, Dickson RC, et al. Improved outcome of orthotopic liver transplantation for chronic hepatitis B cirrhosis with aggressive passive immunization. Transplantation 1996;61:1358-1364. 8629297.
329. Perrillo RP, Wright T, Rakela J, Levy G, Schiff E, Gish R, et al. A multicenter United States-Canadian trial to assess lamivudine monotherapy before and after liver transplantation for chronic hepatitis B. Hepatology 2001;33:424-432. 11172345.
330. Mutimer D, Dusheiko G, Barrett C, Grellier L, Ahmed M, Anschuetz G, et al. Lamivudine without HBIg for prevention of graft reinfection by hepatitis B: long-term follow-up. Transplantation 2000;70:809-815. 11003363.
331. Gane E, Strasser SI, Patterson S, McCaughan GW, Angus PW. A prospective study on the safety and efficacy of lamivudine and adefovir prophylaxis in HBsAg positive liver transplantation candidates. [Abstract]. Hepatology 2007;46(Suppl 1):479A.
332. Han SH, Ofman J, Holt C, King K, Kunder G, Chen P, et al. An efficacy and cost-effectiveness analysis of combination hepatitis B immune globulin and lamivudine to prevent recurrent hepatitis B after orthotopic liver transplantation compared with hepatitis B immune globulin monotherapy. Liver Transpl 2000;6:741-748. 11084061.
333. Markowitz JS, Martin P, Conrad AJ, Markmann JF, Seu P, Yersiz H, et al. Prophylaxis against hepatitis B recurrence following liver transplantation using combination lamivudine and hepatitis B immune globulin. Hepatology 1998;28:585-589. 9696028.
334. Marzano A, Salizzoni M, Debernardi-Venon W, Smedile A, Franchello A, Ciancio A, et al. Prevention of hepatitis B virus recurrence after liver transplantation in cirrhotic patients treated with lamivudine and passive immunoprophylaxis. J Hepatol 2001;34:903-910. 11451175.
335. Steinmuller T, Seehofer D, Rayes N, Müller AR, Settmacher U, Jonas S, et al. Increasing applicability of liver transplantation for patients with hepatitis B-related liver disease. Hepatology 2002;35:1528-1535. 12029640.
337. Gane EJ, Angus PW, Strasser S, Crawford DH, Ring J, Jeffrey GP, et al. Lamivudine plus low-dose hepatitis B immunoglobulin to prevent recurrent hepatitis B following liver transplantation. Gastroenterology 2007;132:931-937. 17383422.
338. Buti M, Mas A, Prieto M, Casafont F, González A, Miras M, et al. Adherence to Lamivudine after an early withdrawal of hepatitis B immune globulin plays an important role in the long-term prevention of hepatitis B virus recurrence. Transplantation 2007;84:650-654. 17876280.
339. Wong SN, Chu CJ, Wai CT, Howell T, Moore C, Fontana RJ, et al. Low risk of hepatitis B virus recurrence after withdrawal of long-term hepatitis B immunoglobulin in patients receiving maintenance nucleos(t)ide analogue therapy. Liver Transpl 2007;13:374-381. 17318855.
340. Dodson SF, de Vera ME, Bonham CA, Geller DA, Rakela J, Fung JJ. Lamivudine after hepatitis B immune globulin is effective in preventing hepatitis B recurrence after liver transplantation. Liver Transpl 2000;6:434-439. 10915164.
341. Angus P, Strasser S, Patterson S, McCaughan G, Gane E. A randomized study to assess the safety and efficacy of adefovir dipivoxil substitution for hepatitis B immune globulin in liver transplantation patients receiving long-term low dose IM HBIg and lamivudine prophylaxis. [Abstarct]. Hepatology 2007;46:238A.
342. Jimenez-Perez M, Saez-Gomez AB, Mongil Poce L, Lozano-Rey JM, de la Cruz-Lombardo J, Rodrigo-Lopez JM. Efficacy and safety of entecavir and/or tenofovir for prophylaxis and treatment of hepatitis B recurrence post-liver transplant. Transplant Proc 2010;42:3167-3168. 20970638.
343. Grellier L, Mutimer D, Ahmed M, Brown D, Burroughs AK, Rolles K, et al. Lamivudine prophylaxis against reinfection in liver transplantation for hepatitis B cirrhosis. Lancet 1996;348:1212-1215. 8898039.
344. Schiff E, Lai CL, Hadziyannis S, Neuhaus P, Terrault N, Colombo M, et al. Adefovir dipivoxil for wait-listed and post-liver transplantation patients with lamivudine-resistant hepatitis B: final long-term results. Liver Transpl 2007;13:349-360. 17326221.
345. Fontana RJ, Hann HW, Wright T, Everson G, Baker A, Schiff ER, et al. A multicenter study of lamivudine treatment in 33 patients with hepatitis B after liver transplantation. Liver Transpl 2001;7:504-510. 11443577.
346. Ben-Ari Z, Mor E, Shapira Z, Tur-Kaspa R. Long-term experience with lamivudine therapy for hepatitis B virus infection after liver transplantation. Liver Transpl 2001;7:113-117. 11172394.
347. Perrillo R, Rakela J, Dienstag J, Levy G, Martin P, Wright T, et al. Lamivudine Transplant Group. Multicenter study of lamivudine therapy for hepatitis B after liver transplantation. Hepatology 1999;29:1581-1586. 10216146.
348. Ben-Ari Z, Pappo O, Zemel R, Mor E, Tur-Kaspa R. Association of lamivudine resistance in recurrent hepatitis B after liver transplantation with advanced hepatic fibrosis. Transplantation 1999;68:232-236. 10440393.
349. Neff GW, O'Brien CB, Nery J, Shire N, Montalbano M, Ruiz P, et al. Outcomes in liver transplant recipients with hepatitis B virus: resistance and recurrence patterns from a large transplant center over the last decade. Liver Transpl 2004;10:1372-1378. 15497163.
350. Karlas T, Hartmann J, Weimann A, Maier M, Bartels M, Jonas S, et al. Prevention of lamivudine-resistant hepatitis B recurrence after liver transplantation with entecavir plus tenofovir combination therapy and perioperative hepatitis B immunoglobulin only. Transpl Infect Dis 2011;13:299-302. 21159112.
351. Cholongitas E, Papatheodoridis GV, Burroughs AK. Liver grafts from anti-hepatitis B core positive donors: A systematic review. J Hepatol 2010;52:272-279. 20034693.
353. Avelino-Silva VI, D'Albuquerque LA, Bonazzi PR, Song AT, Miraglia JL, De Brito Neves A, et al. Liver transplant from Anti-HBc-positive, HBsAg-negative donor into HBsAg-negative recipient: is it safe? A systematic review of the literature. Clin Transplant 2010;24:735-746. 20438579.
354. Gupta S, Govindarajan S, Fong TL, Redeker AG. Spontaneous reactivation in chronic hepatitis B: patterns and natural history. J Clin Gastroenterol 1990;12:562-568. 2230000.
355. Lok AS, McMahon BJ. Chronic hepatitis B: update of recommendations. Hepatology 2004;39:857-861. 14999707.
356. Yeo W, Johnson PJ. Diagnosis, prevention and management of hepatitis B virus reactivation during anticancer therapy. Hepatology 2006;43:209-220. 16440366.
358. Lok AS, Liang RH, Chiu EK, Wong KL, Chan TK, Todd D. Reactivation of hepatitis B virus replication in patients receiving cytotoxic therapy. Report of a prospective study. Gastroenterology 1991;100:182-188. 1983820.
359. Yeo W, Chan PK, Zhong S, Ho WM, Steinberg JL, Tam JS, et al. Frequency of hepatitis B virus reactivation in cancer patients undergoing cytotoxic chemotherapy: a prospective study of 626 patients with identification of risk factors. J Med Virol 2000;62:299-307. 11055239.
361. Kwak LW, Halpern J, Olshen RA, Horning SJ. Prognostic significance of actual dose intensity in diffuse large-cell lymphoma: results of a tree-structured survival analysis. J Clin Oncol 1990;8:963-977. 2348230.
362. Bonadonna G, Valagussa P, Moliterni A, Zambetti M, Brambilla C. Adjuvant cyclophosphamide, methotrexate, and fluorouracil in node-positive breast cancer: the results of 20 years of follow-up. N Engl J Med 1995;332:901-906. 7877646.
363. Yeo W, Chan PK, Hui P, Ho WM, Lam KC, Kwan WH, et al. Hepatitis B virus reactivation in breast cancer patients receiving cytotoxic chemotherapy: a prospective study. J Med Virol 2003;70:553-561. 12794717.
364. Takai S, Tsurumi H, Ando K, Kasahara S, Sawada M, Yamada T, et al. Prevalence of hepatitis B and C virus infection in haematological malignancies and liver injury following chemotherapy. Eur J Haematol 2005;74:158-165. 15654908.
365. Hsu C, Hsiung CA, Su IJ, Hwang WS, Wang MC, Lin SF, et al. A revisit of prophylactic lamivudine for chemotherapy-associated hepatitis B reactivation in non-Hodgkin's lymphoma: a randomized trial. Hepatology 2008;47:844-853. 18302293.
367. Cheng AL, Hsiung CA, Su IJ, Chen PJ, Chang MC, Tsao CJ, et al. Steroid-free chemotherapy decreases risk of hepatitis B virus (HBV) reactivation in HBV-carriers with lymphoma. Hepatology 2003;37:1320-1328. 12774010.
368. Yeo W, Chan TC, Leung NW, Lam WY, Mo FK, Chu MT, et al. Hepatitis B virus reactivation in lymphoma patients with prior resolved hepatitis B undergoing anticancer therapy with or without rituximab. J Clin Oncol 2009;27:605-611. 19075267.
369. Lau GK, Leung YH, Fong DY, Au WY, Kwong YL, Lie A, et al. High hepatitis B virus (HBV) DNA viral load as the most important risk factor for HBV reactivation in patients positive for HBV surface antigen undergoing autologous hematopoietic cell transplantation. Blood 2002;99:2324-2330. 11895763.
370. Lau GK, He ML, Fong DY, Bartholomeusz A, Au WY, Lie AK, et al. Preemptive use of lamivudine reduces hepatitis B exacerbation after allogeneic hematopoietic cell transplantation. Hepatology 2002;36:702-709. 12198664.
371. Dai MS, Wu PF, Shyu RY, Lu JJ, Chao TY. Hepatitis B virus reactivation in breast cancer patients undergoing cytotoxic chemotherapy and the role of preemptive lamivudine administration. Liver Int 2004;24:540-546. 15566502.
373. Shim JH, Park JW, Choi JI, Park BJ, Kim CM. Practical efficacy of sorafenib monotherapy for advanced hepatocellular carcinoma patients in a Hepatitis B virus-endemic area. J Cancer Res Clin Oncol 2009;135:617-625. 18846384.
374. Hui CK, Cheung WW, Zhang HY, Au WY, Yueng YH, Leung AY, et al. Kinetics and risk of de novo hepatitis B infection in HBsAg-negative patients undergoing cytotoxic chemotherapy. Gastroenterology 2006;131:59-68. 16831590.
375. El-Sayed MH, Mohamed MM, Karim A, Maina AM, Oliveri F, Brunetto MR, et al. Severe liver disease is caused by HBV rather than HCV in children with hematological malignancies. Hematol J 2003;4:321-327. 14502256.
376. Yeo W, Chan PK, Ho WM, Zee B, Lam KC, Lei KI, et al. Lamivudine for the prevention of hepatitis B virus reactivation in hepatitis B s-antigen seropositive cancer patients undergoing cytotoxic chemotherapy. J Clin Oncol 2004;22:927-934. 14990649.
377. Chung SJ, Kim JK, Park MC, Park YB, Lee SK. Reactivation of hepatitis B viral infection in inactive HBsAg carriers following anti-tumor necrosis factor-alpha therapy. J Rheumatol 2009;36:2416-2420. 19797507.
379. Kim YJ, Bae SC, Sung YK, Kim TH, Jun JB, Yoo DH, et al. Possible reactivation of potential hepatitis B virus occult infection by tumor necrosis factor-alpha blocker in the treatment of rheumatic diseases. J Rheumatol 2010;37:346-350. 20008922.
380. Alexopoulou A, Theodorou M, Dourakis SP, Karayiannis P, Sagkana E, Papanikolopoulos K, et al. Hepatitis B virus reactivation in patients receiving chemotherapy for malignancies: role of precore stop-codon and basic core promoter mutations. J Viral Hepat 2006;13:591-596. 16907845.
381. Sugauchi F, Tanaka Y, Kusumoto S, Matsuura K, Sugiyama M, Kurbanov F, et al. Virological and clinical characteristics on reactivation of occult hepatitis B in patients with hematological malignancy. J Med Virol 2011;83:412-418. 21264861.
382. Steinberg JL, Yeo W, Zhong S, Chan JY, Tam JS, Chan PK, et al. Hepatitis B virus reactivation in patients undergoing cytotoxic chemotherapy for solid tumours: precore/core mutations may play an important role. J Med Virol 2000;60:249-255. 10630955.
383. Borentain P, Colson P, Coso D, Charbonnier A, Stoppa AM, Auran T, et al. Clinical and virological factors associated with hepatitis B virus reactivation in HBsAg-negative and anti-HBc antibodies-positive patients undergoing chemotherapy and/or autologous stem cell transplantation for cancer. J Viral Hepat 2010;17:807-815. 20002298.
384. Niitsu N, Hagiwara Y, Tanae K, Kohri M, Takahashi N. Prospective analysis of hepatitis B virus reactivation in patients with diffuse large B-cell lymphoma after rituximab combination chemotherapy. J Clin Oncol 2010;28:5097-5100. 20837949.
385. Tanaka Y, Esumi M, Shikata T. Persistence of hepatitis B virus DNA after serological clearance of hepatitis B virus. Liver 1990;10:6-10. 2308481.
386. Koo YX, Tan DS, Tan IB, Tao M, Chow WC, Lim ST. Hepatitis B virus reactivation and role of antiviral prophylaxis in lymphoma patients with past hepatitis B virus infection who are receiving chemoimmunotherapy. Cancer 2010;116:115-121. 19899164.
387. Rossi G, Pelizzari A, Motta M, Puoti M. Primary prophylaxis with lamivudine of hepatitis B virus reactivation in chronic HbsAg carriers with lymphoid malignancies treated with chemotherapy. Br J Haematol 2001;115:58-62. 11722410.
388. Lau GK, Yiu HH, Fong DY, Cheng HC, Au WY, Lai LS, et al. Early is superior to deferred preemptive lamivudine therapy for hepatitis B patients undergoing chemotherapy. Gastroenterology 2003;125:1742-1749. 14724827.
389. Saab S, Dong MH, Joseph TA, Tong MJ. Hepatitis B prophylaxis in patients undergoing chemotherapy for lymphoma: a decision analysis model. Hepatology 2007;46:1049-1056. 17680650.
391. Li HR, Huang JJ, Guo HQ, Zhang X, Xie Y, Zhu HL, et al. Comparison of entecavir and lamivudine in preventing hepatitis B reactivation in lymphoma patients during chemotherapy. J Viral Hepat 2011;18:877-883. 21054683.
392. Lopez-Alcorocho JM, Barril G, Ortiz-Movilla N, Traver JA, Bartolomé J, Sanz P, et al. Prevalence of hepatitis B, hepatitis C, GB virus C/hepatitis G and TT viruses in predialysis and hemodialysis patients. J Med Virol 2001;63:103-107. 11170045.
393. Finelli L, Miller JT, Tokars JI, Alter MJ, Arduino MJ. National surveillance of dialysis-associated diseases in the United States, 2002. Semin Dial 2005;18:52-61. 15663766.
394. Johnson DW, Dent H, Yao Q, Tranaeus A, Huang CC, Han DS, et al. Frequencies of hepatitis B and C infections among haemodialysis and peritoneal dialysis patients in Asia-Pacific countries: analysis of registry data. Nephrol Dial Transplant 2009;24:1598-1603. 19096083.
395. Burdick RA, Bragg-Gresham JL, Woods JD, Hedderwick SA, Kurokawa K, Combe C, et al. Patterns of hepatitis B prevalence and seroconversion in hemodialysis units from three continents: the DOPPS. Kidney Int 2003;63:2222-2229. 12753311.
396. Minuk GY, Sun DF, Greenberg R, Zhang M, Hawkins K, Uhanova J, et al. Occult hepatitis B virus infection in a North American adult hemodialysis patient population. Hepatology 2004;40:1072-1077. 15486926.
397. Gwak GY, Huh W, Lee DH, Min BH, Koh KC, Kim JJ, et al. Occult hepatitis B virus infection in chronic hemodialysis patients in Korea. Hepatogastroenterology 2008;55:1721-1724. 19102377.
398. Kellerman S, Alter MJ. Preventing hepatitis B and hepatitis C virus infections in end-stage renal disease patients: back to basics. Hepatology 1999;29:291-293. 9862883.
399. Miller ER, Alter MJ, Tokars JI. Protective effect of hepatitis B vaccine in chronic hemodialysis patients. Am J Kidney Dis 1999;33:356-360. 10023650.
400. DaRoza G, Loewen A, Djurdjev O, Love J, Kempston C, Burnett S, et al. Stage of chronic kidney disease predicts seroconversion after hepatitis B immunization: earlier is better. Am J Kidney Dis 2003;42:1184-1192. 14655190.
402. Lin CY. Treatment of hepatitis B virus-associated membranous nephropathy with recombinant alpha-interferon. Kidney Int 1995;47:225-230. 7731150.
403. Campistol JM, Esforzado N, Martinez J, Roselló L, Veciana L, Modol J, et al. Efficacy and tolerance of interferon-alpha(2b) in the treatment of chronic hepatitis C virus infection in haemodialysis patients. Pre- and post-renal transplantation assessment. Nephrol Dial Transplant 1999;14:2704-2709. 10534516.
404. Chan TM, Ho SK, Tang CS, Tse KC, Lam MF, Lai KN, et al. Pilot study of pegylated interferon-alpha 2a in dialysis patients with chronic hepatitis C virus infection. Nephrology (Carlton) 2007;12:11-17. 17295655.
405. Ben-Ari Z, Broida E, Kittai Y, Chagnac A, Tur-Kaspa R. An open-label study of lamivudine for chronic hepatitis B in six patients with chronic renal failure before and after kidney transplantation. Am J Gastroenterol 2000;95:3579-3583. 11151895.
406. Boyacioglu S, Gur G, Gursoy M, Ozdemir N. Lamivudine in renal transplant candidates with chronic hepatitis B infection. Transplant Proc 2002;34:2131-2132. 12270341.
407. Schmilovitz-Weiss H, Melzer E, Tur-Kaspa R, Ben-Ari Z. Excellent outcome of Lamivudine treatment in patients with chronic renal failure and hepatitis B virus infection. J Clin Gastroenterol 2003;37:64-67. 12811212.
408. Fontaine H, Thiers V, Chretien Y, Zylberberg H, Poupon RE, Bréchot C, et al. HBV genotypic resistance to lamivudine in kidney recipients and hemodialyzed patients. Transplantation 2000;69:2090-2094. 10852602.
409. Fontaine H, Vallet-Pichard A, Chaix ML, Currie G, Serpaggi J, Verkarre V, et al. Efficacy and safety of adefovir dipivoxil in kidney recipients, hemodialysis patients, and patients with renal insufficiency. Transplantation 2005;80:1086-1092. 16278590.
410. Schiff ER, Lai CL, Hadziyannis S, Neuhaus P, Terrault N, Colombo M, et al. Adefovir dipivoxil therapy for lamivudine-resistant hepatitis B in pre- and post-liver transplantation patients. Hepatology 2003;38:1419-1427. 14647053.
411. Yap DY, Tang CS, Yung S, Choy BY, Yuen MF, Chan TM. Long-term outcome of renal transplant recipients with chronic hepatitis B infection-impact of antiviral treatments. Transplantation 2010;90:325-330. 20562676.
412. Kamar N, Milioto O, Alric L, El Kahwaji L, Cointault O, Lavayssière L, et al. Entecavir therapy for adefovir-resistant hepatitis B virus infection in kidney and liver allograft recipients. Transplantation 2008;86:611-614. 18724232.
413. Ha NB, Ha NB, Garcia RT, Trinh HN, Vu AA, Nguyen HA, et al. Renal dysfunction in chronic hepatitis B patients treated with adefovir dipivoxil. Hepatology 2009;50:727-734. 19517525.
414. Verhelst D, Monge M, Meynard JL, Fouqueray B, Mougenot B, Girard PM, et al. Fanconi syndrome and renal failure induced by tenofovir: a first case report. Am J Kidney Dis 2002;40:1331-1333. 12460055.
415. Gaeta GB, Stornaiuolo G, Precone DF, Lobello S, Chiaramonte M, Stroffolini T, et al. Epidemiological and clinical burden of chronic hepatitis B virus/hepatitis C virus infection. A multicenter Italian study. J Hepatol 2003;39:1036-1041. 14642623.
416. Lee G, Kim KH, Kwon JA, Yoon Sy, Cho Y, Lee CK, et al. Serologic Markers of Viral Hepatitis of Korea University Medical Center Patients. Korean J Lab Med 2005;25:61-65.
417. Lee G, Kim KH, Kwon JA, Yoon SY, Cho Y, Lee CK, et al. Serologic Markers of Viral Hepatitis of Korea University Medical Center Patients. Korean J Lab Med 2005;25:61-65.
418. Sato S, Fujiyama S, Tanaka M, Yamasaki K, Kuramoto I, Kawano S, et al. Coinfection of hepatitis C virus in patients with chronic hepatitis B infection. J Hepatol 1994;21:159-166. 7527435.
419. Lee LP, Dai CY, Chuang WL, Chang WY, Hou NJ, Hsieh MY, et al. Comparison of liver histopathology between chronic hepatitis C patients and chronic hepatitis B and C-coinfected patients. J Gastroenterol Hepatol 2007;22:515-517. 17376043.
420. Sagnelli E, Pasquale G, Coppola N, Scarano F, Marrocco C, Scolastico C, et al. Influence of chronic coinfection with hepatitis B and C virus on liver histology. Infection 2004;32:144-148. 15188073.
421. Kirk GD, Lesi OA, Mendy M, Akano AO, Sam O, Goedert JJ, et al. The Gambia Liver Cancer Study: Infection with hepatitis B and C and the risk of hepatocellular carcinoma in West Africa. Hepatology 2004;39:211-219. 14752840.
422. Benvegnu L, Fattovich G, Noventa F, Tremolada F, Chemello L, Cecchetto A, et al. Concurrent hepatitis B and C virus infection and risk of hepatocellular carcinoma in cirrhosis. A prospective study. Cancer 1994;74:2442-2448. 7922998.
423. Hung CH, Lee CM, Lu SN, Wang JH, Tung HD, Chen CH, et al. Combination therapy with interferon-alpha and ribavirin in patients with dual hepatitis B and hepatitis C virus infection. J Gastroenterol Hepatol 2005;20:727-732. 15853986.
424. Liu CJ, Chen PJ, Lai MY, Kao JH, Jeng YM, Chen DS. Ribavirin and interferon is effective for hepatitis C virus clearance in hepatitis B and C dually infected patients. Hepatology 2003;37:568-576. 12601355.
425. Villa E, Grottola A, Buttafoco P, Colantoni A, Bagni A, Ferretti I, et al. High doses of alpha-interferon are required in chronic hepatitis due to coinfection with hepatitis B virus and hepatitis C virus: long term results of a prospective randomized trial. Am J Gastroenterol 2001;96:2973-2977. 11693335.
426. Liu CJ, Chuang WL, Lee CM, Yu ML, Lu SN, Wu SS, et al. Peginterferon alfa-2a plus ribavirin for the treatment of dual chronic infection with hepatitis B and C viruses. Gastroenterology 2009;136:496-504. 19084016.
427. Kim YJ, Kim JH, Kim YS, Yim HJ, Park YM, Kim BH, et al. Hepatitis B virus coinfected chronic hepatitis C patients: Clinical features and treatment efficacy of peginterferon Alfa-2a plus ribavirin. [Abstract]. Korean J Hepatol 2010;16(Suppl 3):S60.
428. Hadziyannis SJ. Review: hepatitis delta. J Gastroenterol Hepatol 1997;12:289-298. 9195369.
430. Jeong SH, Kim JM, Ahn HJ, Park MJ, Paik KH, Choi W, et al. The prevalence and clinical characteristics of hepatitis-delta infection in Korea. Korean J Hepatol 2005;11:43-50. 15788884.
431. Kim KH, Jung JB, Kang JK, Park IS, Choi HJ, Song KS, et al. Prevalence of Delta antigen among chronic hepatitis B virus infected patients in Korea. Korean J Intern Med 1985;29:30-36.
432. Suh DJ. Delta infection in HBV carriers with chronic liver diseases in Korea. Korean J Intern Med 1985;29:57-61.
433. Fattovich G, Bortolotti F, Donato F. Natural history of chronic hepatitis B: special emphasis on disease progression and prognostic factors. J Hepatol 2008;48:335-352. 18096267.
435. Castelnau C, Le Gal F, Ripault MP, Gordien E, Martinot-Peignoux M, Boyer N, et al. Efficacy of peginterferon alpha-2b in chronic hepatitis delta: relevance of quantitative RT-PCR for follow-up. Hepatology 2006;44:728-735. 16941695.
436. Farci P. Treatment of chronic hepatitis D: New advances, old challenges. Hepatology 2006;44:536-539. 16941704.
437. Farci P, Chessa L, Balestrieri C, Serra G, Lai ME. Treatment of chronic hepatitis D. J Viral Hepat 2007;14(Suppl 1):58-63. 17958644.
438. Farci P, Mandas A, Coiana A, Lai ME, Desmet V, Van Eyken P, et al. Treatment of chronic hepatitis D with interferon alfa-2a. N Engl J Med 1994;330:88-94. 8259188.
439. Niro GA, Ciancio A, Gaeta GB, Smedile A, Marrone A, Olivero A, et al. Pegylated interferon alpha-2b as monotherapy or in combination with ribavirin in chronic hepatitis delta. Hepatology 2006;44:713-720. 16941685.
440. Erhardt A, Gerlich W, Starke C, Wend U, Donner A, Sagir A, et al. Treatment of chronic hepatitis delta with pegylated interferon-alpha2b. Liver Int 2006;26:805-810. 16911462.
441. Yurdaydin C, Bozkaya H, Karaaslan H, Onder FO, Erkan OE, Yalçin K, et al. A pilot study of 2 years of interferon treatment in patients with chronic delta hepatitis. J Viral Hepat 2007;14:812-816. 17927618.
442. Lau DT, Doo E, Park Y, Kleiner DE, Schmid P, Kuhns MC, et al. Lamivudine for chronic delta hepatitis. Hepatology 1999;30:546-549. 10421666.
443. Wedemeyer H, Yurdaydin C, Dalekos GN, Erhardt A, Çakaloğlu Y, Değertekin H, et al. Peginterferon plus adefovir versus either drug alone for hepatitis delta. N Engl J Med 2011;364:322-331. 21268724.
444. Yurdaydin C, Bozkaya H, Onder FO, Sentürk H, Karaaslan H, Akdoğan M, et al. Treatment of chronic delta hepatitis with lamivudine vs lamivudine + interferon vs interferon. J Viral Hepat 2008;15:314-321. 18307594.
445. Brau N, Fox RK, Xiao P, Marks K, Naqvi Z, Taylor LE, et al. Presentation and outcome of hepatocellular carcinoma in HIV-infected patients: a U.S.-Canadian multicenter study. J Hepatol 2007;47:527-537. 17692986.
446. Thio CL, Seaberg EC, Skolasky R Jr, Phair J, Visscher B, Muñoz A, et al. HIV-1, hepatitis B virus, and risk of liver-related mortality in the Multicenter Cohort Study (MACS). Lancet 2002;360:1921-1926. 12493258.
447. Keeffe EB, Marcellin P. New and emerging treatment of chronic hepatitis B. Clin Gastroenterol Hepatol 2007;5:285-294. 17218162.
448. Benhamou Y, Bochet M, Thibault V, Di Martino V, Caumes E, Bricaire F, et al. Long-term incidence of hepatitis B virus resistance to lamivudine in human immunodeficiency virus-infected patients. Hepatology 1999;30:1302-1306. 10534354.
449. Dore GJ, Cooper DA, Pozniak AL, DeJesus E, Zhong L, Miller MD, et al. Efficacy of tenofovir disoproxil fumarate in antiretroviral therapy-naive and -experienced patients coinfected with HIV-1 and hepatitis B virus. J Infect Dis 2004;189:1185-1192. 15031786.
450. Hoff J, Bani-Sadr F, Gassin M, Raffi F. Evaluation of chronic hepatitis B virus (HBV) infection in coinfected patients receiving lamivudine as a component of anti-human immunodeficiency virus regimens. Clin Infect Dis 2001;32:963-969. 11247719.
451. ter Borg MJ, Leemans WF, de Man RA, Janssen HL. Exacerbation of chronic hepatitis B infection after delivery. J Viral Hepat 2008;15:37-41. 18088243.
452. Fontana RJ. Side effects of long-term oral antiviral therapy for hepatitis B. Hepatology 2009;49(5 Suppl):S185-S195. 19399802.
453. del Canho R, Grosheide PM, Mazel JA, Heijtink RA, Hop WC, Gerards LJ, et al. Ten-year neonatal hepatitis B vaccination program, The Netherlands, 1982-1992: protective efficacy and long-term immunogenicity. Vaccine 1997;15:1624-1630. 9364693.
454. Ngui SL, Andrews NJ, Underhill GS, Heptonstall J, Teo CG. Failed postnatal immunoprophylaxis for hepatitis B: characteristics of maternal hepatitis B virus as risk factors. Clin Infect Dis 1998;27:100-106. 9675462.
455. Xu WM, Cui YT, Wang L, Yang H, Liang ZQ, Li XM, et al. Lamivudine in late pregnancy to prevent perinatal transmission of hepatitis B virus infection: a multicentre, randomized, double-blind, placebo-controlled study. J Viral Hepat 2009;16:94-103. 19175878.
456. Han GR, Cao MK, Zhao W, Jiang HX, Wang CM, Bai SF, et al. A prospective and open-label study for the efficacy and safety of telbivudine in pregnancy for the prevention of perinatal transmission of hepatitis B virus infection. J Hepatol 2011;55:1215-1221. 21703206.
457. Hsu HY, Chang MH, Chen DS, Lee CY, Sung JL. Baseline seroepidemiology of hepatitis B virus infection in children in Taipei, 1984: a study just before mass hepatitis B vaccination program in Taiwan. J Med Virol 1986;18:301-307. 2940332.
458. Shah U, Kelly D, Chang MH, Fujisawa T, Heller S, González-Peralta RP, et al. Management of chronic hepatitis B in children. J Pediatr Gastroenterol Nutr 2009;48:399-404. 19322053.
459. Jonas MM, Block JM, Haber BA, Karpen SJ, London WT, Murray KF, et al. Treatment of children with chronic hepatitis B virus infection in the United States: patient selection and therapeutic options. Hepatology 2010;52:2192-2205. 20890947.
460. Sokal EM, Conjeevaram HS, Roberts EA, Alvarez F, Bern EM, Goyens P, et al. Interferon alfa therapy for chronic hepatitis B in children: a multinational randomized controlled trial. Gastroenterology 1998;114:988-995. 9558288.
461. Hom X, Little NR, Gardner SD, Jonas MM. Predictors of virologic response to Lamivudine treatment in children with chronic hepatitis B infection. Pediatr Infect Dis J 2004;23:441-445. 15131468.
462. Kobak GE, MacKenzie T, Sokol RJ, Narkewicz MR. Interferon treatment for chronic hepatitis B: enhanced response in children 5 years old or younger. J Pediatr 2004;145:340-345. 15343187.
464. Lindh M, Uhnoo I, Blackberg J, Duberg AS, Friman S, Fischler B, et al. Treatment of chronic hepatitis B infection: an update of Swedish recommendations. Scand J Infect Dis 2008;40:436-450. 18584530.
465. Jonas MM, Mizerski J, Badia IB, Areias JA, Schwarz KB, Little NR, et al. Clinical trial of lamivudine in children with chronic hepatitis B. N Engl J Med 2002;346:1706-1713. 12037150.
466. Sokal EM, Kelly DA, Mizerski J, Badia IB, Areias JA, Schwarz KB, et al. Long-term lamivudine therapy for children with HBeAg-positive chronic hepatitis B. Hepatology 2006;43:225-232. 16440364.
467. Choe BH, Lee JH, Jang YC, Jang CH, Oh KW, Kwon S, et al. Long-term therapeutic efficacy of lamivudine compared with interferon-alpha in children with chronic hepatitis B: the younger the better. J Pediatr Gastroenterol Nutr 2007;44:92-98. 17204960.
469. Jonas MM, Little NR, Gardner SD. Long-term lamivudine treatment of children with chronic hepatitis B: durability of therapeutic responses and safety. J Viral Hepat 2008;15:20-27. 18088241.
470. Jonas MM, Kelly D, Pollack H, Mizerski J, Sorbel J, Frederick D, et al. Safety, efficacy, and pharmacokinetics of adefovir dipivoxil in children and adolescents (age 2 to <18 years) with chronic hepatitis B. Hepatology 2008;47:1863-1871. 18433023.
Disclosure of conflict of interests for the past 2 years
Process of the revision of 2011 KASL clinical practice guideline for the management of chronic hepatitis B
Flow chart of treatment recommendations based on the virologic response during oral antiviral therapy. Refer to Table 7
for definitions of virologic responses. Low-genetic-barrier drugs include lamivudine, telbivudine, clevudine, and adefovir. High-genetic-barrier drugs include entecavir and tenofovir.
Grading of recommendations, assessment, development and evaluation (GRADE)
Risk factors associated with the development of hepatocellular carcinoma (HCC) and/or cirrhosis in persons with chronic hepatitis B virus
Recommendations for HBsAg-positive person to prevent transmission of HBV to others18
Diagnostic criteria of HBV infection
Initial evaluation of patients with chronic hepatitis B
Adjustment of nucleos(t)ide analogue dosagesfor adult patients with altered creatinine clearance
Definitions of response to antiviral therapy of chronic hepatitis B
Cumulative incidence of antiviral resistance development in representative studies
In vitro cross-resistance of frequent resistant HBV variants
General considerations in the management of antiviral resistance