Discontinuing Immune Checkpoint Inhibitor-Based Therapy After Complete Response in Unresectable Hepatocellular Carcinoma: Evidence, Bias, and a Research Framework.

IF 3.9 3区 医学 Q2 ONCOLOGY
Journal of Hepatocellular Carcinoma Pub Date : 2026-10-09 eCollection Date: 2026-01-01 DOI:10.2147/JHC.S645986
Yujia He, Zhe Wang
{"title":"Discontinuing Immune Checkpoint Inhibitor-Based Therapy After Complete Response in Unresectable Hepatocellular Carcinoma: Evidence, Bias, and a Research Framework.","authors":"Yujia He, Zhe Wang","doi":"10.2147/JHC.S645986","DOIUrl":null,"url":null,"abstract":"<p><p>Immune checkpoint inhibitor (ICI)-based regimens can induce radiographic complete response (CR) in a small but clinically important subset of patients with unresectable hepatocellular carcinoma (HCC). Whether treatment can then be stopped safely remains unresolved. Evidence comes predominantly from retrospective cohorts and post hoc analyses: selected complete responders have durable disease control after cessation, but neither patient-selection criteria nor an optimal post-CR treatment duration has been validated. This structured critical narrative review distinguishes direct evidence in HCC complete responders from indirect HCC studies, local-treatment-assisted CR, and evidence from other tumors. Interpretation depends on the response criterion, confirmation of CR, reason for stopping, residual treatment exposure, and the alignment of treatment assignment with follow-up. Chronic liver disease adds competing mortality and can reduce the opportunity for salvage independently of tumor recurrence. We integrate these issues into a clinical assessment pathway and a framework for prospective research, with attention to recurrence phenotype, hepatic reserve, toxicity, treatment burden, and treatment-free outcomes. Priorities include reproducible CR definitions, longitudinal registries, comparisons of prespecified treatment strategies, and prospective evaluation of surveillance and salvage. Current evidence supports individualized discussion of cessation rather than its routine use after CR or a fixed treatment duration.</p>","PeriodicalId":15906,"journal":{"name":"Journal of Hepatocellular Carcinoma","volume":"13 ","pages":"645986"},"PeriodicalIF":3.9000,"publicationDate":"2026-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13660773/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Hepatocellular Carcinoma","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/JHC.S645986","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Immune checkpoint inhibitor (ICI)-based regimens can induce radiographic complete response (CR) in a small but clinically important subset of patients with unresectable hepatocellular carcinoma (HCC). Whether treatment can then be stopped safely remains unresolved. Evidence comes predominantly from retrospective cohorts and post hoc analyses: selected complete responders have durable disease control after cessation, but neither patient-selection criteria nor an optimal post-CR treatment duration has been validated. This structured critical narrative review distinguishes direct evidence in HCC complete responders from indirect HCC studies, local-treatment-assisted CR, and evidence from other tumors. Interpretation depends on the response criterion, confirmation of CR, reason for stopping, residual treatment exposure, and the alignment of treatment assignment with follow-up. Chronic liver disease adds competing mortality and can reduce the opportunity for salvage independently of tumor recurrence. We integrate these issues into a clinical assessment pathway and a framework for prospective research, with attention to recurrence phenotype, hepatic reserve, toxicity, treatment burden, and treatment-free outcomes. Priorities include reproducible CR definitions, longitudinal registries, comparisons of prespecified treatment strategies, and prospective evaluation of surveillance and salvage. Current evidence supports individualized discussion of cessation rather than its routine use after CR or a fixed treatment duration.

不可切除肝细胞癌完全缓解后停止基于免疫检查点抑制剂的治疗:证据、偏倚和研究框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.50
自引率
2.40%
发文量
108
审稿时长
16 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书