Antagonists of PD-1 and PD-L1 in Cancer Treatment

被引:263
|
作者
Lipson, Evan J. [1 ,2 ]
Forde, Patrick M. [1 ,2 ]
Hammers, Hans-Berg [1 ,2 ]
Emens, Leisha A. [1 ,2 ]
Taube, Janis M. [1 ,2 ,3 ,4 ]
Topalian, Suzanne L. [2 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[2] Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Dermatol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Dept Surg, Baltimore, MD 21205 USA
关键词
TUMOR-INFILTRATING LYMPHOCYTES; ANTI-PD-1; MONOCLONAL-ANTIBODY; RENAL-CELL CARCINOMA; CLINICAL ACTIVITY; NIVOLUMAB ANTI-PD-1; BREAST-CANCER; PATIENTS PTS; ADVANCED MELANOMA; POOR-PROGNOSIS; SAFETY;
D O I
10.1053/j.seminoncol.2015.05.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The PD-1 pathway, comprising the immune cell co-receptor Programmed Death 1 (PD-1) and its ligands, PD-L1 (B7-H1) and PD-L2 (B7-DC), mediates local immunosuppression in the tumor microenvironment. Drugs designed to block PD-1 or PD-L1 "release the brakes" on anti-tumor immunity and have demonstrated clinical activity in several types of advanced cancers, validating this pathway as a target for cancer therapy. Two such drugs have recently been approved to treat melanoma and lung cancers, and regulatory approvals in first- and second-line settings for additional cancer types are anticipated. The manageable safety profile of PD-1/PD-L1 blocking drugs identifies them as suitable for outpatient administration and the development of combinatorial therapies. Ongoing studies aim to identify biomarkers to guide patient selection, which would further improve the risk:benefit ratio for these drugs. (C) 2015 Elsevier Inc. All rights reserved.
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页码:587 / 600
页数:14
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