First-line PD-1/PD-L1 inhibitor plus chemotherapy vs chemotherapy alone for negative or < 1% PD-L1-expressing metastatic non-small-cell lung cancers

被引:16
|
作者
Landre, Thierry [1 ]
Guetz, Gaetan Des [2 ]
Chouahnia, Kader [3 ]
Taleb, Cherifa [4 ]
Vergnenegre, Alain [5 ]
Chouaid, Christos [6 ]
机构
[1] Hop Rene Muret, APHP, UCOG 93, Sevran, France
[2] Ctr Hosp Delafontaine, Serv Oncol Med, St Denis, Reunion, France
[3] Hop Avicenne, APHP, Serv Oncol Med, Bobigny, France
[4] Hop Rene Muret, APHP, Serv Oncogeriatrie, Sevran, France
[5] Unite Oncol Thorac, Serv Oncol Med, Limoges, France
[6] Ctr Hosp Intercommunal CHI Creteil, Serv Pneumol, Creteil, France
关键词
Non-small-cell lung cancer; PD-L1; Anti-PD-1; Immunotherapy; Meta-analysis; Management; Chemotherapy; CHECKPOINT INHIBITORS; DOCETAXEL; NIVOLUMAB;
D O I
10.1007/s00432-019-03070-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims Single-agent anti-PD-1/PD-L1 clinical efficacy against < 1% PD-L1-expressing non-small-cell lung cancers (NSCLCs) is controversial. Methods This meta-analysis examined randomized-trial data comparing first-line PD-1/PD-L1-inhibitor + chemotherapy (CT) vs CT alone for advanced < 1% PD-L1 NSCLCs. Outcome measures included overall survival (OS), progression-free survival (PFS) and objective response rate (ORR). Results IMpower (atezolizumab + CT), Keynote (pembrolizumab + CT) and CheckMate (nivolumab + CT) trials included 2037 NSCLCs (1246 PD-L1-negative; 791 < 1% PD-L1 expression). Anti-PD-1/PD-L1 + CT was significantly associated (hazard ratio [95% confidence interval]) with prolonged OS (0.75 [0.63-0.89]; p = 0.0008) and PFS (0.72 [0.65-0.80]; p < 0.0001), and higher ORR (odds ratio 2.06 [1.50-2.83]; p < 0.0001). Conclusions First-line anti-PD-1/PD-L1 + CT combination appears superior to CT alone for advanced, < 1% PD-L1-expressing NSCLCs for OS, PFS and ORR.
引用
收藏
页码:441 / 448
页数:8
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