医学
肿瘤科
内科学
肺癌
荟萃分析
贝叶斯网络
PD-L1
贝叶斯概率
免疫疗法
癌症研究
癌症
计算机科学
人工智能
作者
Abdulaali R. Almutairi,Nimer S. Alkhatib,Jennifer Martin,Hani M. Babiker,Linda L. Garland,Ali McBride,Ivo Abraham
标识
DOI:10.1016/j.critrevonc.2019.07.004
摘要
Two PD-1 (pembrolizumab, nivolumab) and one PD-L1(atezolizumab) inhibitors are approved for previously treated advanced non-small cell lung cancer but have not been compared in head-to-head trials.A network meta-analysis was conducted to compare efficacy/safety of PD-1/PD-L1 inhibitors.In five-trials (including long-term updates) with docetaxel as common comparator there were no differences in OS and PFS between PD-1/PD-L1 inhibitors. Pembrolizumab (odds ratio(OR) = 2.22, 95%CrI = 1.28-3.70) and nivolumab (OR = 1.92, 95%CrI = 1.15-3.23) had higher ORRs than atezolizumab and at PD-L1 expression ≥50% and ≥1%. Probabilistically, pembrolizumab ranked first in OS and ORR, and in OS sub-analyses for adenocarcinoma, EGFR-mutant, ECOG-score-1, male, and age <65 years. Nivolumab ranked first in PFS, and in OS sub-analyses for squamous-cell disease, EGFR-wild-type, and ECOG-score-0. Pembrolizumab and nivolumab ranked the best option for most of adverse events.While pembrolizumab and nivolumab prevailed in rank in OS and ORR benefit, patient characteristics, safety and tolerance should be considered in treatment decision-making.
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