晚期不可切除肝癌在一线治疗后的全身治疗:来自香港、新加坡和台湾的专家建议。

IF 11.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Liver Cancer Pub Date : 2022-06-17 eCollection Date: 2022-09-01 DOI:10.1159/000525582
Thomas Yau, David Tai, Stephen Lam Chan, Yi-Hsiang Huang, Su Pin Choo, Chiun Hsu, Tan To Cheung, Shi-Ming Lin, Wei Peng Yong, Joycelyn Lee, Thomas Leung, Tracy Shum, Cynthia S Y Yeung, Anna Yin-Ping Tai, Ada Lai Yau Law, Ann-Lii Cheng, Li-Tzong Chen
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引用次数: 9

摘要

背景:由于慢性乙型肝炎感染率高,亚洲的肝细胞癌(HCC)负担高,占全球HCC病例的70%。在过去的20年里,晚期HCC的全身治疗已经发生了巨大的变化——从酪氨酸激酶抑制剂到免疫肿瘤药物加上抗血管内皮生长因子药物。考虑到系统治疗选择的增加,适当的治疗顺序已成为优化患者预后的关键。本文评估了证据,并为晚期HCC患者在一线治疗后使用全身治疗提供了专家建议。摘要:基于2021年初举行的三次虚拟会议,由来自香港、新加坡和台湾的肿瘤学家、肝病学家和肝胆外科医生组成的17名专家组成的团队回顾了一线后肝细胞癌全身治疗的现有数据,并制定了28项声明。这些声明旨在为选择一线和后续治疗提供专家指导,以及在特殊情况下推荐治疗,如肝功能不良、移植后、近期胃肠道出血或自身免疫性疾病。支持这些说法的数据来自临床试验和现实世界的研究。然后使用5分李克特量表对28个陈述进行匿名评估,其中24个达成共识,预定义为达到75%的一致性。产生的陈述包括一线全身治疗的选择、二线全身治疗的考虑和目标、一线治疗后的治疗选择、一线酪氨酸激酶抑制剂、免疫肿瘤单一治疗或免疫肿瘤联合治疗后的治疗建议。作者还分享了对肝功能障碍、肝移植和近期胃肠道或自身免疫性疾病患者使用二线全身治疗的专家意见。关键信息:这些专家陈述总结了一线治疗后选择全身治疗的最新数据和专家意见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systemic Treatment of Advanced Unresectable Hepatocellular Carcinoma after First-Line Therapy: Expert Recommendations from Hong Kong, Singapore, and Taiwan.

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.

Key messages: These expert statements summarize the latest data and expert opinion on selecting systemic treatment following first-line therapy in patients with unresectable advanced or metastatic HCC.

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来源期刊
Liver Cancer
Liver Cancer Medicine-Oncology
CiteScore
20.80
自引率
7.20%
发文量
53
审稿时长
16 weeks
期刊介绍: Liver Cancer is a journal that serves the international community of researchers and clinicians by providing a platform for research results related to the causes, mechanisms, and therapy of liver cancer. It focuses on molecular carcinogenesis, prevention, surveillance, diagnosis, and treatment, including molecular targeted therapy. The journal publishes clinical and translational research in the field of liver cancer in both humans and experimental models. It publishes original and review articles and has an Impact Factor of 13.8. The journal is indexed and abstracted in various platforms including PubMed, PubMed Central, Web of Science, Science Citation Index, Science Citation Index Expanded, Google Scholar, DOAJ, Chemical Abstracts Service, Scopus, Embase, Pathway Studio, and WorldCat.
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