ABSTRACT
Hepatocellular carcinoma (HCC) is the fourth most common cancer and the second leading cause of cancer-related death in Taiwan. The Taiwan Liver Cancer Association and the Gastroenterological Society of Taiwan developed and updated the guidelines for HCC management in 2020. In clinical practice, we follow these guidelines and the reimbursement policy of the government. In Taiwan, abdominal ultrasonography, alpha-fetoprotein, and protein induced by vitamin K absence or antagonist-II (PIVKA-II) tests are performed for HCC surveillance every 6 months or every 3 months for high-risk patients. Dynamic computed tomography, magnetic resonance imaging, and contrast-enhanced ultrasound have been recommended for HCC surveillance in extremely high-risk patients or those with poor ultrasonographic visualization results. HCC is usually diagnosed through dynamic imaging, and pathological diagnosis is recommended. Staging of HCC is based on a modified version of the Barcelona Clinic Liver Cancer (BCLC) system, and the HCC management guidelines in Taiwan actively promote curative treatments including surgery and locoregional therapy for BCLC stage B or C patients. Transarterial chemoembolization (TACE), drug-eluting bead TACE, transarterial radioembolization, and hepatic artery infusion chemotherapy may be administered for patients with BCLC stage B or C HCC. Sorafenib and lenvatinib are reimbursed as systemic therapies, and regorafenib and ramucirumab may be reimbursed in cases of sorafenib failure. First-line atezolizumab with bevacizumab is not yet reimbursed but may be administered in clinical practice. Systemic therapy and external beam radiation therapy may be used in specific patients. Early switching to systemic therapy in TACE-refractory patients is a recent paradigm shift in HCC management.
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Keywords: Liver cancer; Surveillance; Barcelona clinic liver cancer; Surgery; Systemic therapy
INTRODUCTION
Hepatocellular carcinoma (HCC) is the fourth most common cancer in Taiwan. The Taiwan Cancer Registry reported 11,272 new HCC cases in 2019, with a crude incidence rate of 47.76 per 100,000 person-years. Moreover, 7,881 HCC mortalities occurred, and the crude mortality rate was 33.39 per 100,000 person-years; thus, HCC constitutes the second leading cause of cancer-related mortality in Taiwan [
1]. HCC cases in Taiwan are mostly attributable to hepatitis B virus (HBV) in fection (47%), followed by that of hepatitis C virus (HCV) (33%). Active viral replication is the primary mechanism of hepatocarcinogenesis [
2].
Taiwan was the first country to launch nationwide HBV vaccination in 1984 [
3]; this decreased the HBV carriage rate and reduced the risk of developing HCC (as primary prevention) [
4]. Antiviral therapy reduces the risk of HCC caused by both HBV [
5,
6] and HCV (as secondary prevention) [
7]. Antiviral therapy reduces the incidence of recurrence of HBV- and HCV-related HCC after curative therapies (as tertiary prevention) [
8,
9]. The National Health Insurance (NHI) program in Taiwan has reimbursed anti-HBV and anti-HCV therapy since 2003, which has effectively reduced HCC incidence and mortality attributable to viral hepatitis [
10]. The National Hepatitis C Program Office launched a step-wise intervention to eradicate chronic hepatitis C. Since 2017, Taiwan has fully reimbursed prescriptions of direct antiviral agents (DAAs)—initially for patients with cirrhosis and later for patients with viremia regardless of fibrosis status. By June 30, 2022, more than 130,000 patients with chronic hepatitis C had been treated with DAA.
Overall, the incidence of HBV- and HCV-related HCC is decreasing, whereas the incidence of non-HBV- or non-HCV-related HCC is increasing. As in other parts of the world, nonalcoholic steatohepatitis caused by westernization of lifestyle practices or alcoholism is an emerging etiology of HCC. HCC caused by primary biliary cholangitis, autoimmune hepatitis, or aflatoxin is not common in Taiwan. The Taiwan Liver Cancer Association (TLCA) and the Gastroenterological Society of Taiwan (GEST) proposed a management consensus for HCC in 2016 [
1], which was updated in 2020 [
11].
HCC SURVEILLANCE
Clinical guidelines
TLCA guidelines specify that patients with chronic hepatitis B or C and cirrhosis are at high risk of HCC and should enroll in a surveillance program for HCC that provides opportunities for curative treatment and improves overall survival [
12]. Surveillance should be performed using abdominal ultrasonography and alpha-fetoprotein tests (both are covered by the NHI program) at 6-month intervals (with a range of 3–12 months) [
2]. Dynamic computed tomography (CT), magnetic resonance imaging (MRI), or gadolinium ethoxybenzyl-diethylenetriaminepentaacetic acid (Gd-EOB-DTPA)-enhanced MRI (EOB-MRI) may be recommended every 6 to 12 months for extremely high-risk patients and for patients with difficulty in ultrasound imaging of the liver because of liver atrophy, severe obesity, or postoperative deformity [
11]. Kupffer-phase contrast-enhanced ultrasound (CEUS) may also be recommended as a first-line screening tool for HCC in patients with renal dysfunction and liver cirrhosis (
Table 1) [
11,
13,
14].
A major discrepancy exists between the execution of the guidelines and real-world practice due to poor patient adherence to surveillance recommendations. According to the NHI claim database, among 685,000 patients with a primary diagnosis of hepatitis or cirrhosis in 2008, only 13% received ultrasound and alanine aminotransferase examinations every 6months. To facilitate regular surveillance of HCC, the National Health Insurance Administration of Taiwan introduced a medical care improvement plan in 2000 for patients with chronic hepatitis B or C. This patient-centered program is intended to motivate physicians to perform regular ultrasonography for HCC surveillance every 6 months as recommended by the current guidelines and to encourage HCC identification in the early stage through additional reimbursement to institutions. Examination of protein induced by vitamin K absence or antagonist-II (PIVKA-II) every 6 months has been reimbursed by NHI since 2020 for patients with cirrhosis and those receiving curative therapy for HCC. However, EOB-MRI and CEUS are not reimbursed by NHI.
DIAGNOSIS
Radiological diagnosis
In Taiwan, HCC can be diagnosed noninvasively through dynamic contrast-enhanced CT or MRI if a ≥1.0 cm lesion is identified through ultrasound during surveillance [
11]. Furthermore, guidelines in Asian countries, including those of the Japan Society of Hepatology and the Asian Pacific Association for the Study of the Liver (APASL), recommend EOB-MRI as the first-line diagnostic tool because it is more sensitive than dynamic CT for diagnosing HCC [
15,
16]. Additionally, EOBMRI performed after dynamic CT in patients with early-stage HCC can detect additional small nodules, increase the accuracy of cancer staging, and improve outcomes after curative treatment [
17,
18]. However, the cost of EOB-MRI is not covered by the NHI program in Taiwan even though it is categorized as both a first- and second-line imaging diagnostic tool [
10].
The guidelines of the American Association for the Study of Liver Disease (AASLD) standardize the terminology for interpreting imaging features indicating the presence of HCC; the American College of Radiology released the Liver Imaging Reporting and Data System (LI-RADS) in 2011 [
19]. LI-RADS describes the following categorization: LI-RADS 1 (LR-1, definitely benign), LI-RADS 2 (LR-2, probably benign), LI-RADS 3 (LR-3, intermediate probability), LI-RADS 4 (LR-4, probably HCC), LI-RADS 5 (LR-5, definitely HCC), LI-RADS M (LR-M, malignant but not HCC specific), and LI-RADS TIV (LR-TIV, tumor in vein) based on the likelihood of HCC, non-HCC malignancy, and venous tumors. The Taiwan Society of Interventional Radiology has introduced the use of the LI-RADS in clinical practice for liver tumor diagnosis. However, no study has compared the diagnostic performance and clinical value of LI-RADS v2018.
Clinical guideline
The TLCA guidelines support the clinical diagnosis of HCC in high-risk patients with liver nodules of size >1 cm with a background of cirrhosis or chronic hepatitis B or C. This recommendation is in concordance with AASLD, European Association for the Study of the Liver (EASL), APASL, and other guidelines from major academic organizations [
11,
16,
20-
23]. Histological proof is required when the clinical diagnostic criteria of HCC are not satisfied or the diagnosis of HCC is not of high certainty. TLCA guidelines promote an active biopsy strategy and specify the requirement of histological proof for liver tumors. Although histological subtypes and gene signatures have not yet become key informations before HCC treatment, clinical trials and research are dependent on the availability of HCC tissues. Risks associated with biopsy, including bleeding and needle track tumor spreading tumor spreading [
24], although small, should be considered when contemplating tumor biopsy.
Real-world practice
With the recommendation of histological proof in the TLCA guidelines and the increasing number of immunotherapy combination trials in HCC, physicians in Taiwan have adopted a more aggressive attitude toward active tumor biopsy, particularly in medical centers with clinical trial participation. In 2019, 48.2% of HCC diagnoses were supported by pathology or cytology, which contrasts with the rate <40% being supported by pathology or cytology before 2000 according to the Taiwan Cancer Registry report.
STAGING
Clinical practice guidelines
The Barcelona Clinic Liver Cancer (BCLC) staging system stratifies patients with HCC into very early, early, intermediate, and advanced stages, with 5-year survival rates of 40–70%, 14–45%, 6–14%, and 10%, respectively, and the terminal stage, for patients with tumors beyond the transplantation threshold [
25]. Because of improvements in the HCC surveillance program, the proportion of patients with HCC diagnosed in the early stage has increased from 5–10% to 40–60%, leading to more patients eligible for curative treatments [
26].
Accurate identification of the tumor (T) stage is crucial for extending disease-free survival after curative treatment because tumor size, tumor number, and microvascular invasion are significant predictors of survival [
27,
28]. These tumor characteristics can be examined through preoperative imaging such as liver dynamic CT and MRI [
29]. The strengths of MRI include low operator dependence, no radiation exposure, and ability to analyze the whole liver parenchyma. Furthermore, EOB-MRI has detected more HCCs than dynamic CT in 16.4% of patients receiving concurrent EOB-MRI [
17]. Studies have suggested that higher numbers of HCCs necessitate a change in BCLC staging system, TNM staging, and treatment strategy [
18,
30]. However, liver MRI usually do not visualize lung clearly, which may be the most common area of metastasis in HCC. Therefore, additional liver MRI is suggested in patients with very-early to early-stage HCC, and whole-body CT is recommended for patients with intermediate to advanced HCC.
TLCA guidelines recognize the BCLC staging system as the most common in Taiwan in terms of prognostic prediction [
2]. The BCLC staging system used in Taiwan has two modifications from the original system. One is that, since 2002, a single tumor of size >5 cm has been classified as BCLC stage B [
31]; the other is that a patient with Eastern Cooperative Oncology Group (ECOG) performance status 1 can still be classified as stage 0, stage A, or stage B according to the tumor burden (
Table 2). These differences must be noted when comparing the prognosis of patients with HCC of various BCLC stages in Taiwan and with those in other countries. Other staging systems, including the HKLC staging system [
32], CLIP score [
33], Tokyo score [
34], Japan Integrated Staging score [
35], and TNM system, also provide meaningful prognosis predictions. Another key goal of staging systems is to inform treatment selection. Although the BCLC staging system is the most used in Taiwan, the treatment guidance recommended by the BCLC staging system does not reflect true daily practice in Taiwan and other Asian countries. Such practice is characterized by availability of diverse locoregional therapy and endorsement of chemotherapy (systemic and hepatic arterial infusion chemotherapy [HAIC]).
TREATMENT
Surgery and liver transplantation
Surgical intervention plays a major role in HCC management. Taiwan’s 2019 cancer statistics indicate that, among 8,521 patients newly diagnosed with HCC, 2,289 (26.9%) underwent resection and 44 (0.5%) underwent liver transplantation [
36]. Safe liver resection for HCC is performed in accordance with Makuuchi’s criteria including ascites, serum total bilirubin, and indocyanine green clearance tests; these tests are commonly employed to determine the limit of the liver to be resected [
37]. Additionally, in patients without liver cirrhosis, no limitations (e.g., tumor size or number and involvement of portal vein invasion) preclude resection [
2].
Liver reserve is a relative term denoting the interplay between underlying liver disease (cirrhosis, fatty liver, and hepatitis/fibrosis) and the resected functional parenchyma excluding the tumor mass. If the remnant liver reserve is sufficient, the surgical method for HCC resection should be selected based on surgeon capability and experience. Resection can be performed through an open approach or a minimally invasive approach (laparoscopic or robotic assistance); robotic assistance is gaining popularity, with comparable survival duration [
38]. Surgeons can conduct anatomical or parenchymal-sparing (non-anatomical) liver resection. TLCA guidelines recommend a surgical strategy of adequate surgical margin (>1 cm) when possible [
2]. However, a narrow surgical margin, even a null-margin, may achieve cure after resection [
2].
Repeated resection or resection after other local or systemic therapy for HCC recurrence is common in Taiwan. Long-term survival can also be achieved [
39]. Rapid progress of HCC therapeutics (systemic therapy and local treatments) and surgical innovation (Associating Liver Partition and Portal vein Ligation for Staged hepatectomy [ALPPLS]) may further contribute to the trend of treatment migration [
40].
A shortage of transplantable organs from deceased individuals in Taiwan necessitates the development of living-donor liver transplantation. The Milan criteria and UCSF criteria for liver transplantation for eligible patients with HCC are practiced [
2]. Salvage transplantation using liver resection as the primary treatment for patients, followed by transplantation in the event of HCC recurrence or liver failure does not increase the risk of recurrence or similar long-term outcomes compared with primary liver transplantation [
2]. The overall transplantable pool of patients after resection has not decreased [
41]. Downstaging and bridging treatment should be offered to all patients to avoid waitlist dropout. The estimated wait time for transplantation is more than 6 months [
2]. Less strict criteria and incorporation of biological markers are being used in patient selection worldwide, and their long-term effects in Taiwan require investigation [
42].
Radiofrequency ablation (RFA) is a safe and effective curative therapy for patients with very early or early stage HCC who are unsuitable for surgery [
2,
25,
43]. Furthermore, the percutaneous approach for RFA has the advantages of lower morbidity and a shorter length of hospital stay because of its minimal invasiveness [
44]. Because of its safety, simplicity, and low cost, ultrasound is vital in guiding needle insertion and monitoring the ablation effect during RFA [
45,
46]. Moreover, in ultrasound-guided RFA, many strategies (e.g., artificial ascites or pleural effusion creation, real-time ultrasound-CT/MRI fusion imaging, and CEUS) can be used to decrease the incidence of complications and increase the rate of complete ablation [
47,
48]. However, because of the limitations in the ultrasound window and resolution, ultrasound-guided RFA in tumors with difficult locations and poor visibility is associated with a higher local recurrence rate [
49].
In contrast, CT-guided RFA presents no limitation to the depth and field of view. However, one study have reported comparable efficacy and complications between ultrasound- and CT-guided RFA for HCC [
50]. Additionally, the combination of transarterial chemoembolization (TACE) and RFA may lead to longer hospital stays and increased patient discomfort [
51]. Wu et al. [
52] reported that CT-guided RFA after intra-arterial iodized oil injection may achieve more prolonged recurrence-free survival than ultrasound guidance, and that CT-guided RFA is more suitable in this clinical context.
TACE has served as a first-line treatment for intermediate to advanced HCC for over a decade [
43]. Other intra-arterial therapies, such as drug-eluting beads (DEBs), transarterial radioembolization, and HAIC, are available in Taiwan. These techniques provide interventional radiologists in Taiwan with more options for unresectable HCC treatment [
53]. Although the NHI program does not reimburse DEB-TACE or transarterial radioembolization, a consensus exists in Taiwan on the DEB-TACE recommendation, and physicians have experience attending randomized controlled trials of transarterial radioembolization [
54,
55]. HAIC is also recommended for patients with portal vein thrombosis, but no consensus or large-scale randomized controlled trial exists. Practice guidelines recommend DEB-TACE, transarterial radioembolization, and HAIC for patients with multiple tumors or vascular invasion [
11].
SYSTEMIC THERAPY
Clinical guidelines
TLCA guidelines recommends sorafenib and lenvatinib therapy for treatment-naive patients with Child–Pugh A liver function, Eastern Cooperative Oncology Group (ECOG) performance status ≤2, and HCC that is unresectable and not amenable to locoregional therapy [
1] or is refractory to TACE [
11]. Atezolizumab and bevacizumab combination therapy can be used for treating patients with unresectable HCC who have not received prior systemic therapy and do not have a high risk of upper gastrointestinal bleeding [
11]. Sorafenib or nivolumab immunotherapy may be considered for selected patients with Child Pugh class B liver function whose tumors are unresectable and not amenable to locoregional therapy, but the evidence remains insufficient [
11].
In cases of disease progression after sorafenib, additional treatment with regorafenib, cabozantinib, and ramucirumab (when Alpha-fetoprotein ≥400 ng/mL) extend the survival of patients with HCC and Child Pugh class A liver function, whose tumors are unresectable and not amenable to locoregional therapy [
11]. Nivolumab with or without ipilimumab or pembrolizumab can be considered for patients who are intolerant to or have progressed when treated with approved tyrosine kinase inhibitors (
Table 3) [
11,
14,
56-
58].
A paradigm shift in adopting systemic therapy in BCLC stage B HCC has occurred [
59]. TLCA guidelines and clinical studies suggest that targeted therapy combined with TACE can be considered in highly selected patients with unresectable BCLC stage B HCC with Child Pugh class A and ECOG performance status 0-1 [
11].
Because of economic factors, real-world practice mainly depends on the reimbursement criteria of the NHI program. The NHI program has reimbursed sorafenib and lenvatinib as first-line therapy since 2012 and 2020, respectively. To receive sorafenib and lenvatinib treatment, HCC must exhibit extrahepatic spread, major vascular invasion (Vp 2-4), or be refractory to TACE, which is defined as failure to respond to more than 3 TACE sessions within 12 months. Lee et al. [
60] investigated 22 and 44 BCLC stage C patients who received first-line lenvatinib and sorafenib, respectively. The objective response rate (ORR; 36.4% vs. 11.4%,
P=0.023) and disease control rate (DCR) (81.9% vs. 56.9%,
P=0.039) were higher in the lenvatinib group than in the sorafenib group, but patients had a similar overall survival of approximately 9 months [
60].
No first-line immunotherapy is currently reimbursed by the NHI program in Taiwan. In clinical practice, patients receive treatment regimens such as atezolizumab with bevacizumab or lenvatinib with pembrolizumab based on shared decision-making between physician and patient. Shao et al. evaluated 40 participants from Taiwan in the IMbrave 150 and the GO30140 trials. The ORR was 37.5%, including 3 (7.5%) complete responses, and the median duration of response was 21.4 months (95% confidence interval, 16.6-not reached) [
61], which was consistent with the findings for the global intentto-treat populations. Wu et al. [
62] evaluated 71 patients who received lenvatinib plus pembrolizumab for unresectable HCC and reported an ORR of 34.1% in the first-line setting and of 18.5% for systemic therapy-experienced cases. Regorafenib and ramucirumab are reimbursed by the NHI program as second-line therapy in cases of failed first-line sorafenib administration. Nivolumab monotherapy had previously been reimbursed after failure of sorafenib; however, since April 2020, it is no longer reimbursed for new cases.
CLINICAL TRIALS, HEPATIC ARTERY INFUSION CHEMOTHERAPY, SYSTEMIC CHEMOTHERAPY, AND EXTERNAL BEAM RADIATION THERAPY
Clinical trial participation is highly encouraged in Taiwan and is supported by the government (
https://www.taiwanclinicaltrials.tw/). Many landmark trials are spearheaded by investigators in Taiwan, including those for sorafenib (A-P study) [
63], lenvatinib (REFLECT study) [
64], nivolumab (CheckMate 040 study) [
65], and the atezolizumab–bevacizumab combination (IMbrave 150, GO30140) [
66,
67]. Taiwan has an outstanding health-care system with 23 medical centers and up to 99.96% population coverage by the NHI program, which provides an excellent environment for clinical trial implementation. Medical centers in Taiwan actively recruit patients to clinical trials involving early-, intermediate-, and advanced-stage HCC with the belief that all suitable patients should be offered the opportunity to be considered for participation.
TLCA guidelines endorse the use of chemotherapy for HCC as both systemic and locoregional therapy. Systemic chemotherapy commonly demonstrates 5–10% response rates in patients with HCC with acceptable performance status and liver reserve [
68]. However, HAIC is a form of locoregional therapy with a response rate up to 30% and is valuable for intrahepatic tumor control [
69,
70]. A phase III study demonstrated the survival benefit of combining sorafenib with FOLFOX compared with sorafenib alone in patients with portal vein tumor thrombosis (PVTT) [
71]. This response rate of sorafenib with FOLFOX was 40.8%, which may be of great value in patients with large intrahepatic tumor burden or PVTT. Although phase III studies of systemic chemotherapy (FOLFOX, PIAF, or doxorubicin) have not demonstrated a clear survival benefit for patients with advanced HCC [
68,
72] and only one clinical trial reported survival benefit of adding sorafenib to HAIC-FOLFOX, both systemic therapy and HAIC remain in the armamentarium of the physician treating HCC in Taiwan because of the high response rate for intrahepatic tumor control and reimbursement by the NHI program.
TLCA guidelines support the administration of external beam radiation therapy (EBRT), including photon and proton therapy, for various stages of HCC [
2,
73]. For BCLC stage A, EBRT can be considered when HCC is inaccessible to ablation or is unresectable, as a bridge therapy before liver transplantation, or when the patient refuses standard treatment. For BCLC stage B, EBRT can be considered in cases where HCC is inaccessible or unsuitable for TACE or is refractory to TACE, as a bridge to liver transplantation, or when localized tumor with symptoms or a threat to liver reserve is present. For BCLC stage C, EBRT can be considered in patients with portal vein tumor thrombus, in those with HCC unsuitable or refractory to TACE, or in those with a localized tumor with symptoms or a threat to liver reserve. For BCLC stage D, EBRT can be considered for symptomatic metastasis or for oligometastases as palliation. In real practice, EBRT in addition to standard therapy is not uncommon and is favored by a subset of patients and physicians in Taiwan.
DISCUSSION
Because of the high disease burden of HCC and the highquality medical care reimbursed by the NHI program in Taiwan, TLCA guidelines devote considerable attention to preventing the development, pursuing the early diagnosis, and improving the overall survival of HCC. Compared with the BCLC guidelines [
74], TLCA guidelines advocate a more aggressive attitude toward curative treatment (e.g., surgical resection) [
2]. Whenever possible, surgical intervention is considered first for managing HCC. Liver transplantation is not yet widely applied to patients with HCC, even in the setting of living donor predominance.
The introduction of systemic therapy has greatly contributed to the management strategies available for intermediateand advanced-stage HCC. Physicians in Taiwan typically attempt to downstage HCC for curative therapy. The BCLCguided treatment is advanced or modified according to the therapeutic effectiveness of locoregional or systemic therapy in each scenario. For intermediate-stage HCC, systemic therapy may be neoadjuvant, early-switch therapy, adjuvant, or even initial therapy. However, the major limitation is lack of reimbursement by the NHI program in Taiwan. Currently, first-line immunotherapy is not reimbursed, which may reduce the overall treatment responses in advanced HCC.
HCC management is characterized by a constant struggle between treating the tumor and preserving residual liver function. Through a multidisciplinary team approach, application of antiviral therapy, and improvement of supportive care, liver reserve can be maintained after HCC management. In-depth, cross-professional communication between surgeons, hepatologists, oncologists, and interventional radiologists may provide the greatest benefits in caring for patients with HCC.
Randomized phase III trials may not provide optimal benefits for patients with HCC. Thus, in addition to randomized trials, high-quality real-world data and real-world evidence are required and will gradually play a greater role in drug approval. Considerable discrepancies exist between HCC guidelines and real-life practice. Academic organizations should recognize the inherent value of a multidisciplinary team approach in HCC treatment and endorse various modalities that may help patients with HCC.
ACKNOWLEDGMENTS
This work was supported by grants from the Ministry of Science and Technology, Taiwan (grant numbers MOST 109-2326-B-002 -012 -MY3, MOST 110-2326-B-400-004, MOST 110-2628-B-002-041), Ministry of Health and Welfare (MOHW111-TDU-B-221-014003), National Taiwan University Hospital (grant numbers 110-N01, 110-T20), and the Liver Disease Prevention & Treatment Research Foundation, Taiwan.
FOOTNOTES
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Authors’ contribution
Tung-Hung Su: study concept and design, acquisition of data, analysis and interpretation of data, drafting the manuscript. Chih-Horng Wu: acquisition of data, analysis and interpretation of data, drafting the manuscript. Tsung-Hao Liu: acquisition of data, analysis and interpretation of data, drafting the manuscript. Cheng-Maw Ho: acquisition of data, analysis and interpretation of data, drafting the manuscript. Chun-Jen Liu: study concept and design, acquisition of data, analysis and interpretation of data, critical review and revise the manuscript, study supervision.
-
Conflicts of Interest
T.-H. S. received research grant from Gilead Sciences, served as a consultant for Gilead Sciences, and was on speaker’s bureaus for Abbvie, Bayer, Bristol-Myers Squibb, Gilead Sciences, Lilly, Merck Sharp and Dohme, Roche, and Takeda.
Table 1.Comparison of HCC surveillance programs between international and Taiwan guidelines and real-world practice
Table 1.
|
HCC surveillance |
International/other guidelines [13,14,16,20,21] |
Taiwan guideline [2,11] |
Real-world practice |
|
Ultrasound |
Yes |
Yes |
Yes |
|
Alpha-fetoprotein |
No: EASL |
Yes |
Yes |
|
Optional: AASLD |
|
Yes: APASL, NCCN |
|
PIVKA-II |
Yes: JSH |
No |
Yes (cirrhosis/HCC curative therapy) |
|
CT/MRI/CEUS |
CT/MRI in extremely high risk patients (JSH) |
Yes in extremely high risk patients (6–12 months) |
Yes, but not reimbursed by National Health Insurance |
|
Interval |
6 months |
6 months (3–12 months) |
3–12 months |
Table 2.Comparison between the current BCLC staging and the modified BCLC staging used in Taiwan
Table 2.
|
Stage |
BCLC staging system (2022)
|
Modified BCLC staging system used in Taiwan
|
|
Tumor burden |
Liver function |
Performance status |
Tumor burden |
Liver function |
Performance status |
|
0 |
Single ≤2 cm |
Preserved liver function |
0 |
Single ≤2 cm |
Child-Pugh A |
0–1 |
|
A |
Single or ≤3 nodules each ≤3 cm |
Preserved liver function |
0 |
Single ≤5 cm or ≤3 nodules each ≤3 cm |
Child-Pugh A-B |
0–1 |
|
B |
Multinodular |
Preserved liver function |
0 |
Single >5 cm or Multinodular |
Child-Pugh A-B |
0–1 |
|
C |
Portal invasion, N1, M1 |
Preserved liver function |
1–2 |
Portal invasion, N1, M1 |
Child-Pugh A-B |
0–2 |
|
D |
Any |
End-stage liver function |
3–4 |
Any |
Child-Pugh C |
3–4 |
Table 3.Comparison between international and Taiwan guidelines and real-world practice for systemic therapy
Table 3.
|
Systemic treatments |
International guideline |
Taiwan guideline [11] |
Real-world practice |
|
First line |
|
|
|
|
Target therapy |
Sorafenib, [14,56,57,74] lenvatinib [14,56,57,74] |
Sorafenib, lenvatinib |
Sorafenib,* lenvatinib*
|
|
Immunotherapy or immunotherapy combinations |
Atezolizumab+bevacizumab [14,56,57,74] |
Atezolizumab+bevacizumab |
Atezolizumab+bevacizumab, lenvatinib+ pembrolizumab, bevacizumab+anti-PD-1 monoclonal antibody†
|
|
Durvalumab±Tremelimumab [58,74] |
|
Cytotoxic chemotherapy |
No |
Selected patients (regimen not specified) |
FOLFOX, Cisplatin+infusional 5-FU, doxorubicin |
|
Second line |
|
|
|
|
Target therapy |
Regorafenib, [14,56,57,74] cabozantinib, [14,56,57,74] ramucirumab [14,56,57,74] |
Regorafenib, cabozantinib, ramucirumab |
Regorafenib, Ramucirumab |
|
Immunotherapy or immunotherapy combinations |
Nivolumab+ipilimumab, [14,56] Nivolumab, [14,56] pembrolizumab [14,56] |
Nivolumab±ipilimumab, pembrolizumab |
Nivolumab±ipilimumab, pembrolizumab, multikinase inhibitor+anti-PD-1/PD-L1 monoclonal antibody,‡ bevacizumab+anti- PD-1 monoclonal antibody†
|
Abbreviations
protein induced by vitamin K absence or antagonist-II
Barcelona Clinic Liver Cancer
transarterial chemoembolization
National Health Insurance
Taiwan Liver Cancer Association
Gastroenterological Society of Taiwan
magnetic resonance imaging
Gadolinium ethoxybenzyl-diethylenetriaminepentaacetic acid enhanced MRI
contrast-enhanced ultrasound
Asian Pacific Association for the Study of the Liver
American Association for the Study of Liver Disease
Liver Imaging Reporting and Data System
European Association for the Study of the Liver
hepatic arterial infusion chemotherapy
Associating Liver Partition and Portal vein Ligation for Staged hepatectomy
external beam radiation therapy
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