Anti-CTLA-4 Antibody Therapy: Immune Monitoring During Clinical Development of a Novel Immunotherapy

被引:178
作者
Callahan, Margaret K. [1 ,2 ]
Wolchok, Jedd D. [1 ,2 ,3 ]
Allison, James P. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
[2] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[3] Sloan Kettering Inst, Ludwig Ctr Canc Immunotherapy, New York, NY USA
[4] Mem Sloan Kettering Canc Ctr, Dept Immunol, New York, NY 10065 USA
[5] Howard Hughes Med Inst, Chevy Chase, MD USA
关键词
REGULATORY T-CELLS; LYMPHOCYTE-ASSOCIATED ANTIGEN-4; METASTATIC MELANOMA PATIENTS; OVERCOMING IMMUNOLOGICAL-TOLERANCE; PHASE-I TRIAL; CTLA-4; BLOCKADE; COMBINATION IMMUNOTHERAPY; ANTITUMOR IMMUNITY; PROGNOSTIC-FACTORS; TUMOR-REGRESSION;
D O I
10.1053/j.seminoncol.2010.09.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cytotoxic T-lymphocyte-associated antigen (CTLA-4), also known as CD! 52, is a co-inhibitory molecule that functions to regulate T-cell activation. Antibodies that block the interaction of CTLA-4 with its ligands B7.1 and B7.2 can enhance immune responses, including antitumor immunity. Two CTLA-4 - blocking antibodies are presently under clinical investigation: ipilimumab and tremelimumab. CTLA-4 blockade has shown promise in treatment of patients with metastatic melanoma, with a recently completed randomized, double-blind phase III trial demonstrating a benefit in overall survival (OS) in the treated population. However, this approach appears to benefit only a subset of patients. Understanding the mechanism(s) of action of CTLA-4 blockade and identifying prognostic immunologic correlates of clinical endpoints to monitor are presently areas of intense investigation. Several immunologic endpoints have been proposed to correlate with clinical activity. This review will focus on the endpoints of immune monitoring described in studies to date and discuss future areas of additional work needed. Semin Oncol 37:473-484 (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:473 / 484
页数:12
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