ABSTRACT
-
Background/Aims
A comprehensive analysis of trends in the incidence of hepatocellular carcinoma (HCC) is important for planning public health initiatives. We aimed to analyze the trends in HCC incidence in South Korea over 10 years and to predict the incidence for the year 2028.
-
Methods
Data from patients with newly diagnosed HCC between 2008 and 2018 were obtained from Korean National Health Insurance Service database. Age-standardized incidence rates (ASRs) were calculated to compare HCC incidence. A poisson regression model was used to predict the future incidence of HCC.
-
Results
The average crude incidence rate (CR) was 22.4 per 100,000 person-years, and the average ASR was 17.6 per 100,000 person-years between 2008 and 2018. The CR (from 23.9 to 21.2 per 100,000 person-years) and ASR (from 21.9 to 14.3 per 100,000 person-years) of HCC incidence decreased during the past ten years in all age groups, except in the elderly. The ASR of patients aged ≥80 years increased significantly (from 70.0 to 160.2/100,000 person-years; average annual percent change, +9.00%; P<0.001). The estimated CR (17.9 per 100,000 person-years) and ASR (9.7 per 100,000 person-years) of HCC incidence in 2028 was declined, but the number of HCC patients aged ≥80 years in 2028 will be quadruple greater than the number of HCC patients in 2008 (from 521 to 2,055), comprising 21.3% of all HCC patients in 2028.
-
Conclusions
The ASRs of HCC in Korea have gradually declined over the past 10 years, but the number, CR, and ASR are increasing in patients aged ≥80 years.
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Keywords: Age-standardized incidence rate; Hepatocellular carcinoma; Incidence; Korea; Prediction
Study Highlights
• From 2008 to 2018, the incidence of HCC in Korea gradually declined, however, the incidence of HCC patients aged ≥80 years increased significantly (age-standardized incidence rate increased by 0.96% per year).
• In 2028, the number of HCC patients aged ≥80 years will increase to quadruple greater than that in 2008, consisting 21.3% of all HCC patients.
• Investigation in trends of HCC incidence will guide tailored management plan for elderly patients, and will help making a national health strategy to reduce the socioeconomic burden of HCC.
Graphical Abstract
INTRODUCTION
Primary liver cancer is the sixth most common cancer and the third leading cause of cancer-related deaths worldwide [
1,
2]. In 2020, the highest age-standardized incidence rates (ASRs) of liver cancer were observed in Eastern Asia (17.8/100,000 person-years), Northern Africa (15.2/100,000 person-years), South-Eastern Asia (13.7 /100,000 person-years), and South Korea (14.3 cases/100,000 person-years) [
1]. In South Korea, liver cancer ranked second only to lung cancer as a cause of cancer-related deaths in 2016 [
3]. As liver cancer has the highest mortality rate in middle-aged Koreans (i.e., individuals aged 40–59 years) having the highest socioeconomic productivity, there is a substantial disease burden associated with hepatocellular carcinoma (HCC). Therefore, efforts have been continued to accurately investigate the incidence of liver cancer and to establish proper strategies to reduce liver cancer accordingly.
The incidence of liver cancer has been extensively investigated worldwide, but the incidence of HCC is relatively unknown. HCC is the most common primary liver cancer, comprising 75–85% of all primary liver cancers. Most previous studies reported the incidence of all types of cancers in the liver (e.g., intrahepatic cholangiocarcinoma, hepatoblastoma), and thus did not discuss exclusive data about HCC [
1,
4-
6]. In addition, the main source of data for previous epidemiologic studies on HCC in Korea was the Korean Primary Liver Cancer Registry [
7-
10]. Although the data from this registry are representative of patients with HCC nationwide, the registry does not include all patients with HCC.
Hepatitis B virus (HBV), hepatitis C virus (HCV), and liver cirrhosis are risk factors for HCC. In a cohort study concerning the Korean population conducted from 2003–2005, the most frequently identified etiologies of HCC were HBV (62.2%), HCV (10.4%), and alcohol or an unknown etiology (27.4%) [
11]. During the past several decades, many efforts have been made to eradicate HBV, the main cause of HCC. A national project has been in place since 1995 to vaccinate young people against HBV, and patients with chronic hepatitis B (CHB) have been eligible to receive reimbursement for the cost of lifelong antiviral treatment since 2010 [
12]. As a result, HBV infection has decreased dramatically from 8% in the 1990s to 3% in the 2010s in Korea [
12]. However, at the same time, there is an increasing incidence of HCC caused by non-alcoholic fatty liver disease (NAFLD) because of recent westernization of the dietary pattern in Korea [
13,
14]. The improved control of viral hepatitis and increased prevalence of metabolic liver diseases suggest that the etiology of HCC may be changing.
Therefore, it is necessary to comprehensively analyze trends in HCC incidence and the factors that affect these trends. We aimed to analyze the trends in the incidence rates of HCC over 10 years (2008–2018) and to predict the incidence rate of HCC in Korea for the year 2028. In addition, we aimed to study serial changes in the incidence of HCC according to age groups, economic classes, and etiologies.
MATERIALS AND METHODS
Study design
This retrospective cohort study used data from the Korean National Health Insurance Service (KNHIS) database. Data were extracted and coded with an encrypted number, in accordance with the institutional disclosure principle after permission had been obtained from the National Health Corporation. This study was approved by the Institutional Review Board of Hanyang University, Seoul, Republic of Korea (2019-07-014).
Database characteristics
The Korean government created universal health insurance systems in 1989 and consolidated them into a single system in 2000 [
15]. The health insurance system is mandatory for all Korean citizens, and 97.2% of the Korean population has been enrolled in the system since 2018. Data are entered into the KNHIS database when Korean clinics or hospitals submit an insurance claim to the National Health Corporation for their medical services to be reimbursed.
We included patients from the KNHIS database who had been newly diagnosed with HCC (C220 and V193) between January 2008 and December 2018. We excluded patients if any of the following conditions were met: 1) diagnosis with HCC between 2005 and 2006 due to the low reliability of the data from that period; 2) diagnosis with HCC in the 2 years prior to index date; 3) diagnosis with malignancies other than HCC (C codes other than C220 and V193); 4) history of organ transplantation; 5) human immunodeficiency virus infection; or 6) missing patient identification information (age or sex).
Primary and secondary endpoints
The primary endpoints of this study were the change in the incidence rate of HCC over the past 10 years (2008–2018) by age groups and the predicted incidence rate of HCC in Korea for 2028. The secondary endpoints were the changes in the HCC incidence rate according to age groups, economic classes, and etiologies of HCC.
Stratification
Patients were divided into four age groups: 0–29 years, 30–59 years, 60–79 years, and ≥80 years. The economic classes of the study participants were determined by the premiums of their medical insurance. Medical insurance groups were classified into 20 categories (Q1 to Q20) based on their insurance premiums. The Medicare group was excluded from these categories because patients in this group were exempted from paying the insurance premiums. The 20 categories were grouped into Q1–5, Q6–10, Q11–15, and Q16–20. Patients in the Q16–20 group paid the highest premium, and patients in the Q1–5 group paid the lowest premium.
Definition of HCC
The operational definition of HCC included patients who had assigned both the International Classification of Diseases (ICD) code of C220 and the rare incurable disease code of V193 (cancer). If a patient is diagnosed with a cancer and assigned the V193 code, the patient only pays 5% to 10% of the total medical expenses. Cancer patients covered 10% of the total cost in 2008 and 2009; the proportion decreased to 5% in December 2009. Therefore, the KNHIS requests more information at the time of HCC diagnosis, and these patients are strictly monitored by the government. The KNHIS reviewed whether HCC was diagnosed based on histology, dynamic computed tomography, and/or magnetic resonance imaging findings. The imaging findings suggestive of HCC included a liver nodule >1 cm, arterial hypervascularity of the nodule, and washout in the portal venous or delayed phase [
16].
Etiologic diseases (CHB, chronic hepatitis C, alcoholic liver disease, and NALFD) were identified if the code for the disease or prescription of its treatment was assigned in the calendar year containing the index date or within one calendar year before or after this year (3 years). When two or more etiologic factors were present, patients were classified into the class for the higher-ranked condition in the following order: HBV, HCV, alcoholic liver disease, NAFLD, and others. We have added this information to the Methods section. Comorbid conditions (liver cirrhosis, diabetes mellitus, hypertension, chronic kidney disease, other malignancies, cardiovascular diseases, and cerebrovascular diseases) were identified if the relevant ICD codes were assigned twice during the calendar year containing the index date or within one calendar year before or after this year (3 years). Each definition and the relevant ICD codes were depicted in
Supplementary Table 1.
Data are presented as the median (interquartile range) or frequencies with percentages, as appropriate. The 2005 Korean population covered by the KNHIS was used as the standard population for calculation of the ASR. To evaluate trends in the incidence of HCC during the past 10 years, we used the joinpoint regression method to calculate the average annual percent change (AAPC) in incidence rates. We used the Poisson regression model to predict the incidence of HCC. All statistical analyses were performed using SAS software (version 9.4; SAS Institute, Cary, NC, USA) and R software (version 3.6.0; http://cran.r-project.org/). Two-sided P-values <0.05 were considered statistically significant.
RESULTS
Baseline characteristics
We identified 127,426 patients in the KNHIS database who had been newly diagnosed with HCC between 2008 and 2018 (
Supplementary Fig. 1). The baseline characteristics of these patients are summarized in
Table 1. The mean age at the time of HCC diagnosis was 61 years, and there was a male predominance (78.3%). HBV was the most common etiology of HCC, affecting 63.0% of all patients with HCC. The top quarter of medical insurance groups (Q16–20) had the largest proportion of patients with HCC (31.5%). Liver cirrhosis, hypertension, and diabetes mellitus were present in 75.8%, 50.2%, and 37.8% of patients with HCC, respectively.
We identified 127,426 patients newly diagnosed with HCC between 2008 and 2018 from the KNHIS database, yielding an average annual incidence rate of 11,584 patients. The average crude incidence rate (CR) of HCC incidence was 22.4 per 100,000 person-years (
Table 2,
Fig. 1), and the average ASR was 17.6 per 100,000 person-years. HCC was more frequent in men than in women, and the age-standardized male-to-female incidence ratio was 3.49 (95% confidence interval [CI], 3.10–3.72;
P=0.032). The annual numbers of HCC incidence significantly decreased from 2008 to 2018 (from 12,056/year in 2008 to 11,234/year in 2018; AAPC: -0.42%; 95% CI, -0.59 to -0.25;
P<0.001). The decline in annual numbers of HCC incidence was observed for both sexes (AAPC in men, -0.43%; AAPC in women, -0.37%). The CR of HCC incidence decreased from 23.9 per 100,000 person-years in 2008 to 21.2 per 100,000 person-years in 2018, but this change was not statistically significant (AAPC, -0.94%;
P=0.640). The ASR in the entire population significantly decreased from 2008 to 2018 (from 21.9/100,000 person-years in 2008 to 14.3/100,000 person-years in 2018; AAPC, -3.90%; 95% CI, -4.20 to -3.50;
P<0.001). The decline in ASR between 2008 and 2018 was evident in both men (AAPC, -4.20%; 95% CI, -4.70 to -3.70;
P<0.001) and women (AAPC, -3.90%; 95% CI, -5.00 to -2.90;
P<0.001).
HCC was diagnosed most frequently in patients aged 60–79 years (46.9%), followed by patients aged 30–59 years (45.9%), ≥80 years (6.9%), and 0–20 years (0.3%). The ASR significantly decreased in patients aged 0–29 years and 30–59 years (
Table 3,
Supplementary Fig. 2). The decline in annual ASR was greater in patients aged 0–29 years (AAPC, -13.59%; 95% CI, -16.48 to -10.60) than in patients aged 30–59 years (AAPC, -3.10%; 95% CI, -4.10 to -2.10;
P<0.001;
Table 3,
Supplementary Fig. 3). There was a significant decrease in ASR in box sexes in most groups of patients aged <80 years, but patients aged 0–29 women and patients aged 60–79 men did not show significant decrease in ASR. The average annual change was greatest in men aged 0–29 years (AAPC, -14.10%; 95% CI, -19.70 to -8.10;
P<0.001). The numbers of HCC and CR significantly decreased in patients aged 0–29 years and 30–59 years (
Supplementary Table 2). In patients aged 60–79 years, the numbers of HCC did not change, whereas the CR of HCC incidence significantly decreased. The ASR in patients aged ≥80 years increased from 70.0 per 100,000 person-years in 2008 to 160.2 per 100,000 person-years in 2018 (AAPC, 9.00%; 95% CI, 7.90–10.20;
P<0.001;
Fig. 2C). This increase was evident in both men (AAPC, 9.40%; 95% CI, 8.42–10.45;
P<0.001) and women (AAPC, 8.80%; 95% CI, 7.70–9.90;
P<0.001;
Table 3). During the 10-year study period, the numbers of HCC increased in patients aged ≥80 years (AAPC, 9.90%; 95% CI, 7.90–10.20;
P<0.001;
Supplementary Table 2,
Fig. 2A). The CR of HCC incidence in patients aged ≥80 years also significantly increased (AAPC, 1.40%; 95% CI, 0.80–1.90;
P<0.001;
Supplementary Table 2,
Fig. 2B).
Patients with HCC were diagnosed most frequently in the Q16–20 group (31.5%), followed by the Q11–15 (23.7%), Q6–10 (19.5%), Q6–10 (18.6%), and Medicare (6.7%) groups. However, the ASR was significantly greater in the Medicare group than in the Q16–20 group. From 2008 to 2018, there was a significant decrease in the ASR in all groups (
Supplementary Fig. 4,
Supplementary Table 3), except the Medicare group. There was no significant change in the ASR in the Medicare group (AAPC, -1.40%;
P=0.202).
The most common etiology of HCC was HBV (63.0%), followed by NAFLD (10.4%), alcohol (10.1%), and HCV (9.9%;
Fig. 3). The proportion of patients with HBV-related HCC did not significantly change from 2008 to 2018 (
P=0.210). However, the proportion of HBV-related HCC significantly decreased between 2011 and 2018 with an AAPC of -1.40% (95% CI, -2.10 to -0.70;
P<0.001). The proportion of HCV-related HCC significantly increased with an AAPC of 1.00% (95% CI, 0.20–1.90;
P<0.001), contributing to 9.1% of HCC cases in 2008 and 10.0% in 2018. The proportion of alcohol-induced HCC increased from 8.7% in 2008 to 12.3% in 2018 (AAPC, 3.20%; 95% CI, 2.50–3.90;
P<0.001). Specifically, the proportion of NAFLD-related HCC steadily increased from 2008 to 2018 (AAPC, 2.70%; 95% CI, 0.20–5.30;
P<0.001), with a rapid increase from 2011 to 2018 at an average of 5.60% per year (95% CI, 3.20–8.10;
P<0.001).
The observed and predicted trends in HCC incidence among men and women are summarized in
Figure 1 and
Table 4. We predict that number of new HCC patients in 2028 will be 9,663 (7,264 men; 2,399 women). The CR of HCC incidence in 2028 is estimated to be 17.9 per 100,000 personyears (men: 26.7/100,000 person-years; women: 8.9/100,000 person-years). The predicted ASR will decline by 9.7 per 100,000 person-years in 2028. The ASRs in men and women are expected to be 14.3 and 4.1 per 100,000 person-years, respectively. The annual changes of ASR from 2008 to 2028 are expected to be -3.9% (95% CI, -4.0 to -3.8;
P<0.001) for the entire population, -4.1% (95% CI, -4.2 to -4.0;
P<0.001) for men, and -4.0% (95% CI, -4.1 to -3.9;
P<0.001) for women, respectively. From 2008 to 2028, the ASR is expected to significantly decrease in age groups 0–29 and 30–59 years. The annual decrease of ASR from 2008 to 2028 is expected to be the greatest in the age group 0–29 years with an AAPC of -15.7% (95% CI, -16.6 to -14.8;
P<0.001). In 2028, the number of HCC patients aged ≥80 years is estimated to increase quadruple, compared with the number in 2008 (from 521 in 2008 to 2,055 in 2028). The ASR (from 70.0 to 387.6/100,000 person-years) of HCC incidence of that age is also expected to increase, with an annual increase in ASR of 9.3% (95% CI, 9.2– 9.3;
P<0.001).
Figure 4 shows the proportions of HCC cases in different age groups (2008–2018) and the projected proportions in 2028. From 2008 to 2028, the proportions of patients with HCC developing at ages 0–29 years (AAPC, -11.3%; 95% CI, -14.5 to -8.0;
P<0.001), and 30–59 years (AAPC, -5.2%; 95% CI, -5.5 to -4.8;
P<0.001) are estimated to significantly decrease. Conversely, the proportions of HCC patients at ages 60–79 years (AAPC, 1.4%; 95% CI, 1.1–1.8;
P<0.001), and ≥80 years (AAPC, 8.5%; 95% CI, 8.0–9.0;
P<0.001) are estimated to significantly increase. The proportion of HCC patients aged ≥80 years will increase from 4.3% in 2008 to 21.3% in 2028, and it is estimated that patients older than 60 years will comprise 83.1% in 2028.
DISCUSSION
From 2008 to 2018, the numbers and ASRs of HCC significantly decreased. However, in patients aged ≥80 years, the ASR significantly increased by 0.96% per year; the CR of HCC also increased. By 2028, despite the estimated decrease in HCC incidence in the entire population, the incidence and the proportion of HCC patients aged ≥80 years are estimated to increase. To our knowledge, this study is the first to include a large number of patients (n=127,426) from the KNHIS database, which includes most Korean citizens. The inclusion of such a large number of patients has enabled a comprehensive analysis of the longitudinal trends in HCC incidence in Korea. The estimation of the current and future incidences of HCC in different age groups is important for performing an economic evaluation of the burden of HCC and for formulating an appropriate healthcare policy to control HCC.
There are several important clinical implications of this study. First, the decreasing trend in the ASR of HCC incidence in Korea is similar to the trends observed in Asians living in other countries. A recent study by Petrick et al. [
17] estimated the current and future incidences of HCC in the United States. The overall ASR of HCC increased from 2000 to 2012, and the researchers predicted that it would further increase from 2013 to 2030. In contrast, the ASR of HCC in Asians is expected to decrease from 2013 to 2030 by an average of -1.8% each year, and the ASR of HCC in 2030 is estimated to be 15.5 per 100,000 person-years. Another study from the United States reported that the ASR of HCC significantly decreased from 2007 to 2016 at a rate of -2.72% per year in patients with Asian/Pacific islander ethnicity [
18]. Similar to these two studies, the annual decrease in ASR in our study was -3.9% from 2008 to 2018, and the predicted ASR in 2028 is 9.7% per 100,000 person-years. The projected decrease in the ASR and number of patients with HCC in Korea may be a result of better control of HBV and HBV-related HCC. Although HBV remained the strongest contributing factor to HCC in 2018, the total number of patients with HCC and the proportion of cases of HBV-related HCC decreased annually from 2011 to 2018. Nationwide efforts have been made to eradicate HBV, the main cause of HCC. HBV vaccination has been a component of the national vaccination program since 1995; more than 95% of infants are currently vaccinated, which has contributed to a low positivity rate (0.2%) for hepatitis B surface antigen in children [
19]. In addition, the introduction and expansion of insurance coverage of antiviral agents for HBV have improved the control of HBV replication and prevented cirrhosis-related complications and HCC [
20].
Second, the HCC incidence trends varied noticeably among age groups. While the absolute number of HCC cases in patients aged 0–29 years was very few, the annual decrease in the ASR was the greatest in this age group (AAPC, -13.59%), and the incidence is predicted to approach zero by 2028. From 2008 to 2018, the ASR decreased in patients aged 30– 59 years, and it did not change in patients aged 60–79 years. The ASR anticipated to decrease to 15.5/100,000 person-years in patients aged 30–59 years, whereas it is predicted to increase by 103.2 person-years in patients aged 60–79 years by 2028. Despite a gradual decrease in the ASR over time, the socioeconomic burden of HCC is expected to increase because of increasing life expectancy and a greater likelihood of HCC with increasing age in patients with chronic liver disease. Therefore, efforts should be made to control the HCC incidence in middle-aged patients with the highest socioeconomic productivity to alleviate the socioeconomic burden.
Third, it is concerning that the ASR of HCC is not declining in patients receiving Medicare. From 2008 to 2018, the ASR significantly decreased in all medical insurance groups, except the Medicare group. Conversely, there was a slight increase in the ASR from 2012 to 2018 in the Medicare group, although this difference was not statistically significant. It is unclear whether economic class directly affects HCC incidence. In a study by Anyiwe et al. [
21], patients in the lower income groups had an increased risk of HCC compared with those in the highest income group, despite adjustments for age, sex, and area of residence. Although economic class itself was not a risk factor for HCC, many risk factors for HCC were closely related to economic class. In our study, we did not find any differences in HCC etiology among medical insurance groups (
Supplementary Table 4). However, between 2008 and 2018, patients with HBV-related HCC in the Medicare group had significantly less use of antiviral treatment, than patients in the group with the highest medical insurance (Q16–20) (
Supplementary Table 5). Further research is needed to confirm whether the reduced use of antiviral drugs in HBV-infected patients in the Medicare group is linked to uncontrolled viremia and thus affects HCC development.
Fourth, the proportions of patients developing HCC due to HBV and HCV still remained high in 2018, while the proportions of patients with HCC induced by NAFLD and alcoholic liver disease are increasing. In 2016, the World Health Organization set a goal of eliminating HBV and HCV by the year 2030 using prevention and treatment targets that aim to reduce annual deaths by 65%, increase the proportion of treated patients to 80%, and save 7.1 million lives globally [
22]. Consistent with this 2030 eradication strategy, vaccination against HBV and antiviral treatment for HBV and HCV will further reduce the incidence of HCC. However, the proportion of patients with NAFLD-related HCC increased by 2.7% annually in our study. NAFLD is the fastest growing cause of HCC in the United States and United Kingdom [
23,
24]. The prevalence of NAFLD-related HCC is likely to increase concomitantly with the increasing incidence of obesity. Therefore, management of metabolic indices through lifestyle modification is important for reducing the risk of HCC.
Finally, special attention is needed for patients with HCC aged ≥80 years. The absolute number, CR, and ASR of HCC in patients aged ≥80 years has significantly increased from 2008 to 2018, and the incidence is expected to continue increasing until 2028. An increasing trend in the ASR in the elderly population was also identified in a Taiwanese cohort [
25], and the most plausible explanation was that old age is a risk factor for HCC. The increasing incidence of HCC in older age groups is similar to that seen in other cancers. According to annual statistics from the Korean Central Cancer Registry, the proportion patients with gastric cancer aged ≥80 years was 7.5% and 12.7% in 2008 and 2018, respectively. The proportion patients with colon cancer aged ≥80 years was 9.4% in 2008 and 19.0% in 2018. Moreover, elderly patients have many comorbid conditions, such as liver cirrhosis or diabetes mellitus, which may further increase the risk of HCC. In our subgroup analysis of patients with HBV-related HCC, patients aged ≥80 years received significantly less antiviral treatment between 2008 and 2018 than did patients in other age groups (
P<0.001; data not shown). HBV is the most common etiology of HCC; therefore, uncontrolled HBV viremia in elderly patients can be associated with a greater incidence of HCC. This assumption requires subsequent verification in future studies. By 2028, the proportion of patients with HCC aged ≥80 years will increase to 21.3% of all patients with HCC. This is consistent with the report by Kim and Park [
4] that the age distribution of HCC in Korea has shifted towards the right between 2005 and 2014. When we look up the age structure of general population, the number of Koreans aged 80 years or older increased from 2008 to 2018 (number, 890,000 in 2008 to 1,845,000 in 2018; the proportion, 1.8% in 2008 to 3.1% in 2018) [
26]. Therefore, even considering that Korea is becoming an aging society, the proportion of HCC patients aged 80 years or older increased at a faster rate (4.3% in 2008 to 10.6% in 2018). Elderly patients with HCC often have additional comorbid conditions such as diabetes, hypertension, and renal failure; thus, they may not receive adequate treatment because healthcare professionals are concerned about the abilities of these patients to tolerate standard HCC treatment. Conversely, using standard treatment for HCC without considering the frailty of these patients may cause toxicity or fatality. Therefore, guidelines should be formulated for customized management of elderly patients with HCC to improve the treatment and reduce the socioeconomic burden of HCC.
There were several limitations in our study. First, although we included the entire dataset from the KNHIS database in our analysis, the HCC incidence may have been underestimated because some patients with HCC may not have visited any hospital or the disease codes may have been missed. Second, we could not confirm the medical records of included patients from the hospitals; thus, there was a possibility of misclassification or under-/overestimation of HCC, etiologies of HCC, or comorbid conditions. Third, the operational definition of NAFLD-related HCC was somewhat liberal because we included patients with diabetes mellitus and without any other chronic liver diseases. However, NAFLD-related HCC accounted for only 10% of all HCC cases in our study, and this proportion was similar to a previous Korean study about the etiological distribution of HCC [
13]. Fourth, since we could not perform analysis by birth cohort, it was difficult to determine the exact timing of HCC reduction affected by expansion of HBV vaccination or antiviral treatment for HBV and HCV. Finally, prediction of future incidence assumes that past trends will continue; predictions may be inaccurate if there are various changes in the medical environment.
In conclusion, the ASR of HCC in Korea gradually declined over the past 10 years. However, the number, CR, and ASR of HCC are increasing in patients aged ≥80 years. In 2028, the number of HCC patients aged ≥80 years will be quadruple greater than the number of HCC patients in 2008, and 21.3% of all patients with HCC will be in this age group. A customized HCC management plan that considers the age and general health status of these patients is necessary. In addition, a national health strategy should be implemented to manage the economic burden of HCC.
ACKNOWLEDGMENTS
This article was written with cooperation from the National Health Insurance Service (NHIS) and Korean Association for the Study of the Liver (KASL), based on a MOU (NHIS-2021-1- 096). Data from the National Health Insurance Database of NHIS Korea were analyzed. This study was supported by the Research Supporting Program of The KASL (recipient: S. W. J, KASL 2019-05), and the Soonchunhyang University Research Fund.
SUPPLEMENTARY MATERIAL
Supplementary material is available at Clinical and Molecular Hepatology website
http://www.e-cmh.org.
Supplementary Figure 1.
chart of patient selection in the present study. HCC, hepatocellular carcinoma; KNHIS, Korean National Health Insurance Service.
Supplementary Figure 3.
Age-standardized incidence rate of hepatocellular carcinoma by age groups. (A) Patients aged 0–29 years; (B) patients aged 30–59 years; (C) patients aged 60–79 years.
FOOTNOTES
-
Authors’ contribution
Soung Won Jeong and Dae Won Jun take responsibility for the integrity of the work, from inception tothe published article.
Specific author contributions: Conception: Young Eun Chon, Soung Won Jeong, and Dae Won Jun; Study design: Young Eun Chon, Dae Won Jun, and Soung Won Jeong; Contribution to data acquisition: Young Eun Chon, Seong Yong Park, Eileen Yoon, Soon Sun Kim, Sang Bong Ahn, Soung Won Jeong, and Dae Won Jun; Statistical analysis: Young Eun Chon, Seong Yong Park, Han Pyo Hong, Donghee Son, Jonghyun Lee, Soung Won Jeong, and Dae Won Jun; Writing papers: Young Eun Chon, Soung Won Jeong, and Dae Won Jun.
All authors have reviewed the paper and approved the final version.
-
Conflicts of Interest
The authors have no conflicts to disclose.
Figure 1.Annual incidence rate of hepatocellular carcinoma (2008–2018) and projections of incidence to 2028. (A) Numbers; (B) crude incidence rates (CRs); (C) age-standardized incidence rates (ASRs).
Figure 2.Annual incidence rate of hepatocellular carcinoma (2008–2018) in patients aged ≥80 years. (A) Numbers; (B) crude incidence rates (CRs); (C) age-standardized incidence rates (ASRs).
Figure 3.Annual changes in etiologies of hepatocellular carcinoma (2008–2018). HBV, hepatitis B virus; HCV, hepatitis C virus; NAFLD, non-alcoholic fatty liver disease.
Figure 4.Annual proportions of hepatocellular carcinoma cases according to age groups (2008–2018) and projection in 2028.
Table 1.Baseline characteristics of the study population
Table 1.
|
Variable |
Patients with HCC (n=127,426) |
|
Age (years) |
61.4 (53.0–70.0) |
|
Male gender |
99,767 (78.3) |
|
Etiology |
|
|
HBV |
80,354 (63.0) |
|
HCV |
12,556 (9.9) |
|
Alcohol |
12,815 (10.1) |
|
NAFLD |
13,183 (10.3) |
|
Others |
8,518 (6.7) |
|
District |
|
|
Seoul |
23,428 (18.4) |
|
Medical insurances |
|
|
Medicare |
8,580 (6.7) |
|
Q1–5 |
23,716 (18.6) |
|
Q6–10 |
24,852 (19.5) |
|
Q11–15 |
30,223 (23.7) |
|
Q16–20 |
40,055 (31.5) |
|
Comorbid conditions |
|
|
Liver cirrhosis |
96,593 (75.8) |
|
Chronic kidney disease |
10,619 (8.3) |
|
Diabetes mellitus |
48,182 (37.8) |
|
Hypertension |
63,991 (50.2) |
|
Other neoplasms |
6,766 (5.3) |
|
Cardiovascular diseases |
9,272 (7.3) |
|
Cerebrovascular diseases |
15,962 (12.5) |
Table 2.Annual incidence rate and average annual percent change of hepatocellular carcinoma (2008–2018)
Table 2.
|
All |
2008 |
2009 |
2010 |
2011 |
2012 |
2013 |
2014 |
2015 |
2016 |
2017 |
2018 |
AAPC |
95% CI |
P-value |
|
Numbers |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
127,426 |
12,056 |
11,744 |
11,544 |
11,788 |
11,518 |
11,415 |
11,455 |
11,501 |
11,714 |
11,457 |
11,234 |
-0.42 |
-0.59 to -0.25 |
<0.001 |
|
Men |
99,767 |
9,422 |
9,165 |
9,005 |
9,206 |
9,104 |
9,013 |
9,017 |
9,022 |
9,136 |
8,900 |
8,777 |
-0.43 |
-0.63 to -0.24 |
<0.001 |
|
Women |
27,659 |
2,634 |
2,579 |
2,539 |
2,582 |
2,414 |
2,402 |
2,438 |
2,479 |
2,578 |
2,557 |
2,457 |
-0.37 |
-0.75 to -0.01 |
0.048 |
|
CR (per 100,000 person-years) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
22.4 |
23.9 |
23.2 |
22.6 |
23.0 |
22.3 |
22.0 |
22.0 |
21.9 |
22.2 |
21.7 |
21.2 |
-0.94 |
-4.78 to 3.06 |
0.640 |
|
Men |
35.0 |
37.3 |
36.1 |
35.2 |
35.8 |
35.2 |
34.8 |
34.6 |
34.4 |
34.7 |
33.7 |
33.1 |
-0.92 |
-4.00 to 2.26 |
0.567 |
|
Women |
9.7 |
10.5 |
10.2 |
10.0 |
10.1 |
9.4 |
9.3 |
9.3 |
9.4 |
9.8 |
9.7 |
9.3 |
-0.94 |
-6.70 to 5.18 |
0.758 |
|
ASR (per 100,000 person-years) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
17.6 |
21.9 |
20.5 |
19.3 |
19.0 |
17.8 |
17.2 |
16.7 |
16.1 |
15.9 |
15.1 |
14.3 |
-3.90 |
-4.20 to -3.50 |
<0.001 |
|
Men |
26.9 |
33.7 |
31.4 |
29.6 |
29.0 |
27.5 |
26.4 |
25.5 |
24.6 |
24.0 |
22.7 |
21.6 |
-4.20 |
-4.70 to -3.70 |
<0.001 |
|
Women |
7.7 |
9.6 |
9.1 |
8.5 |
8.4 |
7.6 |
7.3 |
7.1 |
7.0 |
7.0 |
6.7 |
6.2 |
-3.90 |
-5.00 to -2.90 |
<0.001 |
Table 3.Annual age-standardized incidence rate of hepatocellular carcinoma by age
Table 3.
|
Age |
2008 |
2009 |
2010 |
2011 |
2012 |
2013 |
2014 |
2015 |
2016 |
2017 |
2018 |
AAPC |
95% CI |
P-value |
|
Total (per 100,000 person-years) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
21.9 |
20.5 |
19.3 |
19.0 |
17.8 |
17.2 |
16.7 |
16.1 |
15.9 |
15.1 |
14.3 |
-3.90 |
-4.20 to -3.50 |
<0.001 |
|
Men |
33.7 |
31.4 |
29.6 |
29.0 |
27.5 |
26.4 |
25.5 |
24.6 |
24.0 |
22.7 |
21.6 |
-4.20 |
-4.70 to -3.70 |
<0.001 |
|
Women |
9.6 |
9.1 |
8.5 |
8.4 |
7.6 |
7.3 |
7.1 |
7.0 |
7.0 |
6.7 |
6.2 |
-3.90 |
-5.00 to -2.90 |
<0.001 |
|
0–29 years (per 100,000 person-years) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
0.4 |
0.3 |
0.2 |
0.2 |
0.1 |
0.1 |
0.1 |
0.1 |
0.1 |
0.1 |
0.1 |
-13.59 |
-16.48 to -10.60 |
<0.001 |
|
Men |
0.5 |
0.3 |
0.3 |
0.2 |
0.2 |
0.1 |
0.1 |
0.1 |
0.1 |
0.1 |
0.1 |
-14.10 |
-19.70 to -8.10 |
<0.001 |
|
Women |
0.2 |
0.2 |
0.2 |
0.2 |
0.0 |
0.1 |
0.1 |
0.0 |
0.0 |
0.1 |
0.1 |
-44.60 |
-88.80 to 166.20 |
0.400 |
|
30–59 years (per 100,000 person-years) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
25.8 |
25.7 |
25.1 |
25.6 |
24.2 |
23.8 |
23.1 |
22.5 |
21.9 |
20.6 |
19.2 |
-3.10 |
-4.10 to -2.10 |
<0.001 |
|
Men |
42.9 |
43.0 |
42.1 |
42.8 |
40.8 |
40.4 |
39.2 |
37.6 |
36.9 |
34.3 |
32.2 |
-2.80 |
-3.60 to -2.10 |
<0.001 |
|
Women |
8.0 |
7.7 |
7.4 |
7.7 |
7.0 |
6.7 |
6.6 |
7.0 |
6.4 |
6.4 |
5.7 |
-2.80 |
-3.60 to -2.10 |
<0.001 |
|
60–79 years (per 100,000 person-years) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
97.5 |
92.8 |
90.5 |
92.2 |
92.9 |
91.2 |
93.1 |
94.7 |
99.5 |
98.4 |
98.5 |
0.20 |
-0.90 to 1.30 |
0.708 |
|
Men |
163.6 |
154.0 |
150.7 |
154.3 |
158.8 |
156.1 |
159.6 |
163.8 |
171.1 |
172.0 |
173.0 |
0.70 |
-0.20 to 1.60 |
0.129 |
|
Women |
46.3 |
45.3 |
43.9 |
44.0 |
41.7 |
40.9 |
41.6 |
41.1 |
43.9 |
41.4 |
40.9 |
-1.00 |
-1.70 to -0.40 |
0.007 |
|
≥80 years (per 100,000 person-years) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
All |
70.0 |
70.6 |
80.4 |
86.3 |
89.4 |
99.3 |
110.4 |
123.3 |
134.4 |
149.5 |
160.2 |
9.00 |
7.90 to 10.2 |
<0.001 |
|
Men |
137.3 |
131.9 |
149.0 |
163.5 |
174.3 |
187.9 |
213.6 |
248.4 |
255.6 |
279.6 |
318.0 |
9.40 |
8.42 to 10.45 |
<0.001 |
|
Women |
41.5 |
44.6 |
51.3 |
53.6 |
53.4 |
61.8 |
66.6 |
70.2 |
83.1 |
94.4 |
93.4 |
8.80 |
7.70 to 9.90 |
<0.001 |
Table 4.Projections of hepatocellular carcinoma incidence to 2028 in Korea
Table 4.
|
Number of new cases
|
Crude rate (per 100,000 person-years)
|
Age-standardized rate (per 100,000 person-years)
|
|
2008 |
2028 |
Change in numbers (%) |
2008 |
2028 |
Changes in crude rate (%) |
2008 |
2028 |
Changes in ASR (%) |
Annual percent change |
95% CI |
|
All |
12,056 |
9,663 |
-19.8 |
23.9 |
17.9 |
-25.3 |
21.9 |
9.7 |
-55.8 |
-3.9*
|
-4.0 to -3.8 |
|
Men |
9,422 |
7,264 |
-22.9 |
37.3 |
26.7 |
-28.4 |
33.7 |
14.3 |
-57.6 |
-4.1*
|
-4.2 to -4.0 |
|
Women |
2,634 |
2,399 |
-8.9 |
10.5 |
8.9 |
-15.1 |
9.6 |
4.1 |
-57.0 |
-4.0*
|
-4.1 to -3.9 |
|
0–29 years |
75 |
5 |
-93.3 |
0.4 |
0.05 |
-87.5 |
0.4 |
0.01 |
-97.0 |
-15.7*
|
-16.6 to -14.8 |
|
30–59 years |
5,861 |
1,635 |
-72.1 |
24.7 |
7.0 |
-71.7 |
25.8 |
15.5 |
-39.8 |
-2.7*
|
-2.8 to -2.6 |
|
60–79 years |
5,599 |
5,968 |
6.6 |
87.2 |
42.9 |
-50.8 |
97.5 |
103.2 |
5.8 |
0.6*
|
0.5 to 0.6 |
|
≥80 years |
521 |
2,055 |
294.4 |
58.5 |
82.2 |
40.5 |
70.0 |
387.6 |
453.5 |
9.3*
|
9.2 to 9.3 |
Abbreviations
average annual percent change
age-standardized incidence rate
International Classification of Diseases
Korean National Health Insurance Service
nonalcoholic fatty liver disease
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, Dae Won Jun7
