Checkpoint Modulation in Melanoma: An Update on Ipilimumab and Future Directions

被引:14
|
作者
Page, David B. [1 ]
Postow, Michael A. [1 ]
Callahan, Margaret K. [1 ]
Wolchok, Jedd D. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
关键词
Ipilimumab; Checkpoint; Immunotherapy; Melanoma; Anti-programmed cell death 1; PHASE-II TRIAL; METASTATIC MELANOMA; TUMOR MICROENVIRONMENT; MALIGNANT-MELANOMA; ANTIGEN-4; BLOCKADE; ANTITUMOR IMMUNITY; BRAIN METASTASES; CTLA-4; OPEN-LABEL; ANTIBODY;
D O I
10.1007/s11912-013-0337-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ipilimumab, an anti-cytotoxic T-lymphocyte antigen 4 antibody, was the first therapy demonstrated to improve overall survival in melanoma. Since ipilimumab's approval by the FDA in 2011, a wealth of data has amassed, helping clinicians to optimize its use. We have learned how to mitigate the adverse effects of ipilimumab, identified its effects in melanoma subpopulations such as those with brain metastases, uveal melanoma, and mucosal melanoma, discovered potential biomarkers of activity, and investigated its use in combination with other therapeutic modalities. These discoveries have paved the way for rapid development of second-generation immunomodulatory antibodies such as inhibitors of the programmed cell death 1 receptor axis. These new agents hold promise as monotherapy, but perhaps the greatest allure lies in the possibility of combining these agents in synergistic multidrug regimens.
引用
收藏
页码:500 / 508
页数:9
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