Immune Checkpoint Blockade in Cancer Therapy

被引:2127
作者
Postow, Michael A. [1 ,2 ]
Callahan, Margaret K. [1 ,2 ]
Wolchok, Jedd D. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
[2] Weill Cornell Med Coll, New York, NY USA
关键词
LYMPHOCYTE-ASSOCIATED ANTIGEN-4; RESISTANT PROSTATE-CANCER; CELL LUNG-CANCER; METASTATIC MELANOMA; CTLA-4; BLOCKADE; ADVERSE EVENTS; OPEN-LABEL; AUTOIMMUNE HYPOPHYSITIS; MONOCLONAL-ANTIBODY; ANTITUMOR IMMUNITY;
D O I
10.1200/JCO.2014.59.4358
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunologic checkpoint blockade with antibodies that target cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) and the programmed cell death protein 1 pathway (PD-1/PD-L1) have demonstrated promise in a variety of malignancies. Ipilimumab (CTLA-4) and pembrolizumab (PD-1) are approved by the US Food and Drug Administration for the treatment of advanced melanoma, and additional regulatory approvals are expected across the oncologic spectrum for a variety of other agents that target these pathways. Treatment with both CTLA-4 and PD-1/PD-L1 blockade is associated with a unique pattern of adverse events called immune-related adverse events, and occasionally, unusual kinetics of tumor response are seen. Combination approaches involving CTLA-4 and PD-1/PD-L1 blockade are being investigated to determine whether they enhance the efficacy of either approach alone. Principles learned during the development of CTLA-4 and PD-1/PD-L1 approaches will likely be used as new immunologic checkpoint blocking antibodies begin clinical investigation. (C) 2015 by American Society of Clinical Oncology
引用
收藏
页码:1974 / U161
页数:10
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