Predictive effect of PD-L1 expression for immune checkpoint inhibitor (PD-1/PD-L1 inhibitors) treatment for non-small cell lung cancer: A meta-analysis

无容量 阿替唑单抗 医学 彭布罗利珠单抗 危险系数 内科学 肿瘤科 PD-L1 肺癌 荟萃分析 生物标志物 科克伦图书馆 免疫疗法 癌症 置信区间 化学 生物化学
作者
Binbin Zhang,Yi Liu,Sijing Zhou,Huihui Jiang,Ke Zhu,Ran Wang
出处
期刊:International Immunopharmacology [Elsevier BV]
卷期号:80: 106214-106214 被引量:48
标识
DOI:10.1016/j.intimp.2020.106214
摘要

Programmed death-ligand-1 (PD-L1) is a well-known predictive biomarker in non-small cell lung cancer (NSCLC) patients, however, its accuracy remains controversial. Here, we investigated the correlation between PD-L1 expression level and efficacy of its inhibitors, and hence assessed the predictive effect of PD-L1 expression.Studies that evaluated the efficacy of programmed death-1 (PD-1)/ PD-L1 inhibitors in advanced NSCLC patients according to tumor PD-L1 expression levels were searched for on Medline, Cochrane Library, and Embase. The pooled risk ratio (RR) and 95% confidence intervals (95% CIs) were calculated for the objective response rate (ORR) with overall survival (OS) and progression-free survival (PFS) were measured in terms of hazard ratio (HR) and the corresponding 95% CIs.1432 NSCLC patients from six randomized controlled trials (RCTs) were included and three PD-1/PD-L1 inhibitors (atezolizumab, nivolumab, and pembrolizumab) were used to treat the patients. A significantly higher ORR was observed in the high PD-L1 expression group compared to the low expression group (0.35 [95% CI, 0.30-0.40] vs 0.11 [95% CI, 0.09-0.14]). The results of the subgroup analysis, grouped by the type of drugs and antibodies which assess immune checkpoint inhibitors were identical with the pooled result. However, our study showed that PD-L1 expression was neither prognostic nor predictive of overall survival (OS) or progression-free survival (PFS) in patients treated with PD-1/PD-L1 inhibitors compared to chemotherapy.PD-L1 can be a predictive biomarker for ORR. Nevertheless, PD-L1 expression is not a good predictive tool for OS and PFS.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
orixero应助勤恳的从波采纳,获得10
刚刚
hayden发布了新的文献求助10
1秒前
1234hai发布了新的文献求助10
1秒前
1秒前
鹿七七啊完成签到 ,获得积分10
1秒前
jojodan应助大大怪采纳,获得10
1秒前
fmd123发布了新的文献求助10
2秒前
可爱的函函应助sonder采纳,获得10
2秒前
3秒前
xingyi发布了新的文献求助10
3秒前
祖f完成签到,获得积分10
4秒前
ChengYonghui完成签到,获得积分10
4秒前
所所应助kkk采纳,获得10
4秒前
4秒前
boltos完成签到,获得积分10
4秒前
彭于彦祖应助liars采纳,获得30
5秒前
5秒前
范范范发布了新的文献求助10
6秒前
脑洞疼应助qweasdzxcqwe采纳,获得30
6秒前
6秒前
思苇完成签到,获得积分10
6秒前
7秒前
飘逸秋荷发布了新的文献求助10
7秒前
lw发布了新的文献求助10
8秒前
8秒前
简单酸奶完成签到,获得积分10
9秒前
9秒前
dddd完成签到,获得积分10
9秒前
林小雨完成签到,获得积分10
9秒前
a水爱科研完成签到,获得积分10
9秒前
量子星尘发布了新的文献求助10
10秒前
干脆苹果发布了新的文献求助10
10秒前
10秒前
乐观囧发布了新的文献求助10
10秒前
10秒前
Jaho完成签到,获得积分10
10秒前
sci完成签到 ,获得积分10
11秒前
Oyster发布了新的文献求助30
12秒前
北珏完成签到,获得积分10
13秒前
13秒前
高分求助中
A new approach to the extrapolation of accelerated life test data 1000
‘Unruly’ Children: Historical Fieldnotes and Learning Morality in a Taiwan Village (New Departures in Anthropology) 400
Indomethacinのヒトにおける経皮吸収 400
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 330
Robot-supported joining of reinforcement textiles with one-sided sewing heads 320
Aktuelle Entwicklungen in der linguistischen Forschung 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3986829
求助须知:如何正确求助?哪些是违规求助? 3529292
关于积分的说明 11244137
捐赠科研通 3267685
什么是DOI,文献DOI怎么找? 1803843
邀请新用户注册赠送积分活动 881223
科研通“疑难数据库(出版商)”最低求助积分说明 808600