Anti-programmed cell death protein-1/ligand-1 therapy in different cancers

被引:208
作者
Moreno, B. Homet [1 ]
Ribas, A. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, Dept Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Surg, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Med & Mol Pharmacol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, JCCC, Los Angeles, CA 90095 USA
关键词
ANTI-PD-L1; ANTIBODY; ADVANCED MELANOMA; PD-1; BLOCKADE; REGULATORY T; LIGAND; EXPRESSION; SAFETY; IPILIMUMAB; NIVOLUMAB; RESPONSES;
D O I
10.1038/bjc.2015.124
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunologic checkpoint blockade with antibodies against the programmed cell death protein-1 (PD-1) or its ligand (PD-L1) is an effective method for reversing cancer immunosuppression and thereby promoting immune responses against several cancer types. Anti-PD-1 and anti-PD-L1 antibodies have resulted in long-term responses with minimal side effects in significant numbers of patients with melanoma, lung, kidney, bladder and triple-negative breast cancer, as well as in chemotherapy-refractory Hodgkin disease. There is already evidence from at least one randomised trial that anti-PD-1 therapy is superior to chemotherapy in the treatment of patients with metastatic melanoma, and two anti-PD-1 antibodies, pembrolizumab and nivolumab, have been approved by the US Food and Drug Administration for the treatment of patients previously treated for metastatic melanoma. It is anticipated that approvals by drug regulatory bodies will be forthcoming in several cancers in the next months.
引用
收藏
页码:1421 / 1427
页数:7
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