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Article: Systemic Treatment of Advanced Unresectable Hepatocellular Carcinoma after First-Line Therapy: Expert Recommendations from Hong Kong, Singapore, and Taiwan

TitleSystemic Treatment of Advanced Unresectable Hepatocellular Carcinoma after First-Line Therapy: Expert Recommendations from Hong Kong, Singapore, and Taiwan
Authors
Issue Date17-Jun-2022
PublisherKarger Publishers
Citation
Liver Cancer, 2022, v. 11, n. 5, p. 426-439 How to Cite?
Abstract

Background: Asia has a high burden of hepatocellular carcinoma (HCC) due to the high rates of chronic hepatitis B infection and accounts for 70% of HCC cases globally. In the past 20 years, the systemic treatment landscape of advanced HCC has evolved substantially - from tyrosine kinase inhibitors to immune-oncology agents plus anti-vascular endothelial growth factor agents. The appropriate sequence of therapies has become critical in optimizing patient outcomes given the increase in systemic therapeutic options. This article evaluates the evidence and provides expert recommendations for the use of systemic therapies after first-line treatment in patients with advanced HCC.

Summary: Based on three virtual meetings held in early 2021, a team of 17 experts comprising oncologists, a hepatologist, and a hepatobiliary surgeon from Hong Kong, Singapore, and Taiwan reviewed available data about systemic treatments for HCC after first line and formulated 28 statements. These statements aimed to provide expert guidance on selecting first and subsequent lines of therapies as well as recommending therapies in special circumstances, such as poor liver function, posttransplantation, recent gastrointestinal bleeding, or autoimmune diseases. Data supporting the statements were drawn from clinical trials and real-world studies. The 28 statements were then evaluated anonymously using a 5-point Likert scale, and 24 reached consensus, predefined as achieving 75% agreement. Statements generated covered the selection of first-line systemic therapy, considerations and goals of second-line systemic therapies, treatment selection following first-line therapy, and treatment recommendations following first-line tyrosine kinase inhibitors, immune-oncology monotherapy, or immune-oncology combination therapy. The authors also shared expert opinion on the use of second-line systemic therapy in patients with liver dysfunction, liver transplantation, and recent gastrointestinal or autoimmune disease.


Persistent Identifierhttp://hdl.handle.net/10722/359728
ISSN
2023 Impact Factor: 11.6
2023 SCImago Journal Rankings: 3.599

 

DC FieldValueLanguage
dc.contributor.authorYau, Thomas-
dc.contributor.authorTai, David-
dc.contributor.authorChan, Stephen Lam-
dc.contributor.authorHuang, Yi-Hsiang-
dc.contributor.authorChoo, Su Pin-
dc.contributor.authorHsu, Chiun-
dc.contributor.authorCheung, Tan To-
dc.contributor.authorLin, Shi-Ming-
dc.contributor.authorYong, Wei Peng-
dc.contributor.authorLee, Joycelyn-
dc.contributor.authorLeung, Thomas-
dc.contributor.authorShum, Tracy-
dc.contributor.authorYeung, Cynthia S.Y.-
dc.contributor.authorTai, Anna Yin-Ping-
dc.contributor.authorLaw, Ada Lai Yau-
dc.contributor.authorCheng, Ann-Lii-
dc.contributor.authorChen, Li-Tzong-
dc.date.accessioned2025-09-10T00:31:07Z-
dc.date.available2025-09-10T00:31:07Z-
dc.date.issued2022-06-17-
dc.identifier.citationLiver Cancer, 2022, v. 11, n. 5, p. 426-439-
dc.identifier.issn2235-1795-
dc.identifier.urihttp://hdl.handle.net/10722/359728-
dc.description.abstract<p><strong>Background: </strong>Asia has a high burden of hepatocellular carcinoma (HCC) due to the high rates of chronic hepatitis B infection and accounts for 70% of HCC cases globally. In the past 20 years, the systemic treatment landscape of advanced HCC has evolved substantially - from tyrosine kinase inhibitors to immune-oncology agents plus anti-vascular endothelial growth factor agents. The appropriate sequence of therapies has become critical in optimizing patient outcomes given the increase in systemic therapeutic options. This article evaluates the evidence and provides expert recommendations for the use of systemic therapies after first-line treatment in patients with advanced HCC.</p><p><strong>Summary: </strong>Based on three virtual meetings held in early 2021, a team of 17 experts comprising oncologists, a hepatologist, and a hepatobiliary surgeon from Hong Kong, Singapore, and Taiwan reviewed available data about systemic treatments for HCC after first line and formulated 28 statements. These statements aimed to provide expert guidance on selecting first and subsequent lines of therapies as well as recommending therapies in special circumstances, such as poor liver function, posttransplantation, recent gastrointestinal bleeding, or autoimmune diseases. Data supporting the statements were drawn from clinical trials and real-world studies. The 28 statements were then evaluated anonymously using a 5-point Likert scale, and 24 reached consensus, predefined as achieving 75% agreement. Statements generated covered the selection of first-line systemic therapy, considerations and goals of second-line systemic therapies, treatment selection following first-line therapy, and treatment recommendations following first-line tyrosine kinase inhibitors, immune-oncology monotherapy, or immune-oncology combination therapy. The authors also shared expert opinion on the use of second-line systemic therapy in patients with liver dysfunction, liver transplantation, and recent gastrointestinal or autoimmune disease.</p>-
dc.languageeng-
dc.publisherKarger Publishers-
dc.relation.ispartofLiver Cancer-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleSystemic Treatment of Advanced Unresectable Hepatocellular Carcinoma after First-Line Therapy: Expert Recommendations from Hong Kong, Singapore, and Taiwan-
dc.typeArticle-
dc.identifier.doi10.1159/000525582-
dc.identifier.volume11-
dc.identifier.issue5-
dc.identifier.spage426-
dc.identifier.epage439-
dc.identifier.eissn1664-5553-
dc.identifier.issnl1664-5553-

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