Ipilimumab and nivolumab in advanced hepatocellular carcinoma after failure of prior immune checkpoint inhibitor-based combination therapies: a multicenter retrospective study

无容量 易普利姆玛 医学 内科学 联合疗法 肿瘤科 肝细胞癌 贝伐单抗 实体瘤疗效评价标准 癌症 胃肠病学 外科 临床研究阶段 免疫疗法 临床试验 化疗
作者
Daniel Roessler,Osman Öcal,Alexander Philipp,Daniel Markwardt,S Munker,Julia Mayerle,Leonie S. Jochheim,Katharina Hammer,Christian M. Lange,Andreas Geier,Max Seidensticker,Florian P. Reiter,Enrico N. De Toni,Najib Ben Khaled
出处
期刊:Journal of Cancer Research and Clinical Oncology [Springer Science+Business Media]
卷期号:149 (7): 3065-3073 被引量:2
标识
DOI:10.1007/s00432-022-04206-8
摘要

Abstract Introduction Immune checkpoint inhibitor (ICI)-based regimens are transforming the landscape of hepatocellular carcinoma (HCC) treatment. We describe the effect of combined ipilimumab and nivolumab in patients with advanced HCC after the failure of prior ICI-based combination treatments. Methods The clinical course of patients with advanced HCC who received combined ipilimumab and nivolumab after prior ICI-based combination therapies was assessed. Progression-free survival (PFS), overall response rate (ORR) and disease control rate (DCR) per RECIST v1.1 and mRECIST, overall survival (OS), and safety were analyzed. Results Of 109 patients treated with atezolizumab and bevacizumab or other ICI-based combination treatments, ten patients received subsequent therapy with ipilimumab and nivolumab. The majority of patients had Barcelona Clinic Liver Cancer (BCLC) Stage C (80%) HCC and a preserved liver function as defined by Child–Pugh A (80%). At a median follow-up of 15.3 months, ORR for ipilimumab and nivolumab was 30% with a DCR of 40%. Median PFS was 2.9 months and the median OS was 7.4 months. Conclusion This retrospective study demonstrates that combined ipilimumab and nivolumab can be effective and tolerable after prior ICI-based combination therapies and provides a rationale for the prospective clinical evaluation of this treatment sequencing.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
悲凉的幻巧完成签到 ,获得积分10
刚刚
英姑应助大神装采纳,获得10
刚刚
刚刚
Lucas应助proteo采纳,获得10
刚刚
刚刚
上官若男应助大神装采纳,获得10
1秒前
科研通AI6.2应助大神装采纳,获得10
1秒前
十二应助楠楠DAYTOY采纳,获得10
1秒前
ddsyg126完成签到,获得积分10
1秒前
tingalan发布了新的文献求助10
1秒前
是哈密瓜大王完成签到,获得积分10
1秒前
缥缈的觅风完成签到 ,获得积分10
1秒前
xuxu完成签到 ,获得积分10
1秒前
突突突完成签到 ,获得积分20
2秒前
甜蜜一兰发布了新的文献求助10
2秒前
2秒前
yi完成签到,获得积分10
2秒前
wuzhizhongbin完成签到,获得积分10
3秒前
wxm完成签到,获得积分10
3秒前
嘉梦完成签到,获得积分10
3秒前
AAA发布了新的文献求助10
3秒前
Lydia完成签到,获得积分10
3秒前
秋风应助belly采纳,获得10
4秒前
小雯钱来完成签到,获得积分10
4秒前
4秒前
4秒前
crystal发布了新的文献求助10
4秒前
ahaha完成签到,获得积分10
5秒前
Zxz完成签到,获得积分10
5秒前
正直的绮南完成签到 ,获得积分10
5秒前
xyx2999发布了新的文献求助10
6秒前
6秒前
老和山完成签到,获得积分10
6秒前
7秒前
飘逸谷蕊发布了新的文献求助10
7秒前
科研通AI6.4应助飘逸的达采纳,获得10
7秒前
无穷爱科研完成签到,获得积分10
7秒前
123发布了新的文献求助10
7秒前
忐忑的远山完成签到,获得积分10
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The anomeric effect 1000
Principles of town planning: translating concepts to applications 1000
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Perfectionism in School: When Achievement Is not So Perfect 600
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7726651
求助须知:如何正确求助?哪些是违规求助? 9278850
关于积分的说明 20129835
捐赠科研通 7303669
什么是DOI,文献DOI怎么找? 3302240
关于科研通互助平台的介绍 2455591
邀请新用户注册赠送积分活动 2310164