PD-1/PD-L1 inhibitors

被引:420
|
作者
Sunshine, Joel [1 ]
Taube, Janis M. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Med Inst, Dept Dermatol, Baltimore, MD 21205 USA
[2] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Dept Oncol, Baltimore, MD 21205 USA
关键词
ANTI-PD-1; MONOCLONAL-ANTIBODY; CLINICAL ACTIVITY; PATIENTS PTS; NIVOLUMAB ANTI-PD-1; PD-L1; EXPRESSION; SAFETY; EFFICACY; IPILIMUMAB; RESPONSES; MELANOMA;
D O I
10.1016/j.coph.2015.05.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tumors may adopt normal physiologic checkpoints for immunomodulation leading to an imbalance between tumor growth and host surveillance. Antibodies targeting the PD-1/PD-L1 checkpoint have shown dynamic and durable tumor regressions, suggesting a rebalancing of the host tumor interaction. Nivolumab and pembrolizumab are the anti-PD-1 antibodies that are currently the furthest in clinical development, and anti-PD-L1 agents under investigation include MPDL3280A, MEDI4736, and BMS-936559. These agents have been used to treat advanced melanoma, non-small cell lung cancer, renal cell carcinoma, bladder cancer and Hodgkin lymphoma, amongst other tumor types. In this article, we review the updated response results for early clinical trials, note recent FDA actions regarding this class of agents, and summarize results across trials looking at PD-L1 status as a predictor of response to anti-PD-1/PD-L1.
引用
收藏
页码:32 / 38
页数:7
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