Nivolumab plus ipilimumab in non-small-cell lung cancer

被引:43
|
作者
Reck, Martin [1 ]
Borghaei, Hossein [2 ]
O'Byrne, Kenneth J. [3 ,4 ]
机构
[1] German Ctr Lung Res, Airway Res Ctr North, LungenClin Grosshansdorf, Woehrendamm 80, D-22927 Grosshansdorf, Germany
[2] Fox Chase Canc Ctr, Dept Hematol Oncol, Div Thorac Med Oncol, 333 Cottman Ave, Philadelphia, PA 19111 USA
[3] Princess Alexandra Hosp, Translat Res Inst, Brisbane, Qld 4102, Australia
[4] Queensland Univ Technol, Brisbane, Qld 4102, Australia
关键词
atezolizumab; CTLA-4; immunotherapy; ipilimumab; nivolumab; non-small-cell lung cancer; pembrolizumab; PD-1; PD-L1; tumor mutational burden; TUMOR MUTATIONAL BURDEN; OPEN-LABEL; PHASE-III; ANTI-PD-1; ANTIBODY; 1ST-LINE TREATMENT; STAGE IV; MAINTENANCE BEVACIZUMAB; CTLA-4; BLOCKADE; SOLID TUMORS; DOCETAXEL;
D O I
10.2217/fon-2019-0031
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nivolumab and ipilimumab, two therapeutic immune checkpoint inhibitor antibodies that block PD-1 and CTLA-4, respectively, have indications in cancer as single agents and in combination. In this Review, we examine the potential role of dual immune checkpoint inhibition with nivolumab plus ipilimumab in the management of patients with previously untreated advanced non-small-cell lung cancer, based on results from the Phase III CheckMate 227 study. Immunotherapies with indications in the first-line treatment of non-small-cell lung cancer include pembrolizumab alone and combined with chemotherapy, and atezolizumab combined with bevacizumab and chemotherapy. CheckMate 227 is the first Phase III study evaluating first-line chemotherapy-sparing combination immunotherapy and including tumor mutational burden as a biomarker for patient selection.
引用
收藏
页码:2287 / 2302
页数:16
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