Department of Pharmacy Practice and Science, College of Pharmacy, University of Arizona, Tucson, AZ, USA; Center for Health Outcomes and PharmacoEconomic Research, College of Pharmacy, University of Arizona, Tucson, AZ, USA.
Department of Pharmacy Practice and Science, College of Pharmacy, University of Arizona, Tucson, AZ, USA; Arizona Health Sciences Library, University Libraries, University of Arizona, Tucson, AZ, USA.
Crit Rev Oncol Hematol. 2019 Oct;142:16-25. doi: 10.1016/j.critrevonc.2019.07.004. Epub 2019 Jul 10.
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.
两种 PD-1(派姆单抗、纳武利尤单抗)和一种 PD-L1(阿替利珠单抗)抑制剂已被批准用于治疗先前治疗的晚期非小细胞肺癌,但尚未在头对头试验中进行比较。
进行了一项网络荟萃分析,以比较 PD-1/PD-L1 抑制剂的疗效/安全性。
在五项试验(包括长期更新)中,以多西他赛为共同比较剂,PD-1/PD-L1 抑制剂在 OS 和 PFS 方面无差异。派姆单抗(优势比(OR)=2.22,95%可信区间(CrI)=1.28-3.70)和纳武利尤单抗(OR=1.92,95%CrI=1.15-3.23)的 ORR 高于阿替利珠单抗,在 PD-L1 表达≥50%和≥1%时也是如此。概率上,派姆单抗在 OS 和 ORR 方面排名第一,在腺癌、EGFR 突变、ECOG 评分 1、男性和年龄<65 岁的 OS 亚分析中也是如此。纳武利尤单抗在 PFS 方面排名第一,在鳞状细胞疾病、EGFR 野生型和 ECOG 评分 0 的 OS 亚分析中也是如此。派姆单抗和纳武利尤单抗在大多数不良反应方面是最佳选择。
虽然派姆单抗和纳武利尤单抗在 OS 和 ORR 获益方面排名靠前,但在治疗决策中应考虑患者特征、安全性和耐受性。