Impact of Bevacizumab Being Skipped due to Adverse Events of Special Interest for Bevacizumab in Patients with Unresectable Hepatocellular Carcinoma Treated with Atezolizumab plus Bevacizumab: An Exploratory Analysis of the Phase III IMbrave150 Study

贝伐单抗 阿替唑单抗 医学 内科学 危险系数 肿瘤科 不利影响 肝细胞癌 实体瘤疗效评价标准 胃肠病学 临床研究阶段 临床试验 无容量 癌症 置信区间 化疗 免疫疗法
作者
Masatoshi Kudo,Kaoru Tsuchiya,Yu‐Yun Shao,Richard S. Finn,Peter R. Galle,Michel Pierre Ducreux,Ann‐Lii Cheng,Tatsuya Yamashita,Hironori Koga,Ryosuke Take,Kyoko Yamada,Takashi Asakawa,Yuki Nakagawa,Masafumi Ikeda
出处
期刊:Liver cancer [Karger Publishers]
卷期号:13 (4): 401-412 被引量:22
标识
DOI:10.1159/000535501
摘要

Introduction: The phase III IMbrave150 study established atezolizumab + bevacizumab as the global standard of care in patients with unresectable hepatocellular carcinoma (HCC). This exploratory analysis examined the impact of bevacizumab interruption due to bevacizumab adverse events of special interest (AESIs). Methods: Patients in IMbrave150 who were randomized to atezolizumab + bevacizumab and received treatment for ≥6 months (to reduce immortal time bias) were included in group A-1 if bevacizumab had ever been skipped due to bevacizumab AESIs or to group A-2 otherwise. Efficacy analyses included overall survival (OS) and progression-free survival (PFS) by whether bevacizumab was skipped (group A-1 vs. A-2). PFS was evaluated per independent review facility (IRF)-assessed Response Evaluation Criteria in Solid Tumours (RECIST) version 1.1 and HCC-modified RECIST (IRF-HCC mRECIST). Safety was also evaluated. Results: Of the 210 patients who received ≥6 months of atezolizumab + bevacizumab, 69 were assigned to group A-1 and 141 to A-2. At data cutoff (August 20, 2020), hazard ratio (HR) for OS was 1.04 (95% CI: 0.64, 1.69) for group A-1 versus A-2. HR for PFS was 1.07 (95% CI: 0.74, 1.55) per IRF-assessed RECIST 1.1 and 1.10 (95% CI: 0.76, 1.59; 15.5 vs. 9.7 months) per IRF-HCC mRECIST for group A-1 versus A-2. Safety profiles for atezolizumab and bevacizumab were largely similar between groups. More group A-1 patients had grade 3/4 adverse events. A separate analysis investigating the impact of immortal time bias in patients who received ≥3 months of atezolizumab + bevacizumab supported the appropriateness of the ≥6-month landmark analysis. Discussion/Conclusion: Efficacy was similar between patients who skipped bevacizumab due to bevacizumab AESIs and those who did not. Although this comparison was nonrandomized and exploratory, results suggest that skipping bevacizumab due to bevacizumab AESIs did not considerably impact the efficacy and safety of atezolizumab + bevacizumab.
最长约 10秒,即可获得该文献文件

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
XiaoNing发布了新的文献求助10
刚刚
乐乐的应助被Liusy采纳,获得10
刚刚
1秒前
1秒前
1秒前
Lucas的应助被深林狼采纳,获得10
1秒前
名取周一发布了新的文献求助10
1秒前
1秒前
1秒前
1秒前
xuzhu0907发布了新的文献求助10
2秒前
灵巧的应助被天天采纳,获得10
2秒前
Brighter16发布了新的文献求助10
2秒前
科研通AI6.4的应助被天天采纳,获得10
2秒前
2秒前
852的应助被ddz采纳,获得10
3秒前
爆米花的应助被科研人采纳,获得10
3秒前
04d的应助被天天采纳,获得10
3秒前
3秒前
领导范儿的应助被天天采纳,获得10
3秒前
MYXuan发布了新的文献求助10
3秒前
打打的应助被天天采纳,获得10
3秒前
莲花盛开的应助被天天采纳,获得10
3秒前
研友_VZG7GZ的应助被天天采纳,获得30
3秒前
Orange的应助被天天采纳,获得30
4秒前
mate发布了新的文献求助10
4秒前
可爱的函函的应助被天天采纳,获得10
4秒前
丁丁完成签到,获得积分10
4秒前
小汤圆发布了新的文献求助10
4秒前
4秒前
4秒前
Raven完成签到,获得积分10
4秒前
Li发布了新的文献求助10
5秒前
huang的应助被violetlishu采纳,获得10
5秒前
爱博发布了新的文献求助20
5秒前
NexusExplorer的应助被大头会说话采纳,获得10
6秒前
玉簪完成签到,获得积分10
6秒前
6秒前
英姑的应助被十七采纳,获得10
6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
Energie-Contracting 1500
Klimaschutzrecht durch den Energiesektor im Mehrebenensystem – Ein Rechtsvergleich 1000
Stochastic Models in Operations Research,Vol. 2 600
Critical Bildung: Hegel and the Logic of Diremption 500
桑白皮エキスの実験的, 臨床的育毛効果について 500
Qualitative Methodologies in Tourism Studies: Disrupting and Co-creating Critical Research 350
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8036893
求助须知:如何正确求助?哪些是违规求助? 9472607
关于积分的说明 21260928
捐赠科研通 7606351
什么是DOI,文献DOI怎么找? 3390256
关于科研通互助平台的介绍 2522089
邀请新用户注册赠送积分活动 2427501