Immunotherapy in the treatment of non-small cell lung cancer

被引:100
|
作者
Sundar, Raghav [1 ]
Soong, Richie [2 ,3 ]
Cho, Byoung-Chul [4 ]
Brahmer, Julie R. [5 ]
Soo, Ross A. [1 ,2 ,6 ]
机构
[1] Natl Univ Hlth Syst, Natl Univ Canc Inst, Dept Haematol Oncol, Singapore 119228, Singapore
[2] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore 117548, Singapore
[3] Natl Univ Hlth Syst, Dept Pathol, Singapore 119228, Singapore
[4] Yonsei Canc Ctr, Div Med Oncol, Seoul, South Korea
[5] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Baltimore, MD USA
[6] Univ Western Australia, Dept Surg, Nedlands, WA 6009, Australia
基金
新加坡国家研究基金会;
关键词
Immunotherapy; Non-small cell lung cancer; PD-L1; CTLA-4; Ipilimumab; Nivolumab; TUMOR-NECROSIS-FACTOR; LYMPHOCYTE-ASSOCIATED ANTIGEN-4; REGULATORY T; INFILTRATING LYMPHOCYTES; COSTIMULATORY MOLECULE; ANTI-CTLA-4; ANTIBODY; LIGAND-1; EXPRESSION; DRIVER MUTATIONS; CD40; DOUBLE-BLIND;
D O I
10.1016/j.lungcan.2014.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Advances in the understanding of the role of the immune system in tumor immunosurveillance have resulted in the recognition that tumors can evade immune destruction via the dysregulation of co-inhibitory or checkpoint signals. This has led to the development of a generation immunotherapeutic agents targeting the immune checkpoint pathway. Recent early phase studies of immune checkpoint modulators, such as CTLA-4, PD-1 and PD-L1 inhibitors in NSCLC have reported promising results with prolonged clinical responses and tolerable toxicity. This article provides an overview of co-stimulatory and inhibitory molecules that regulate the immune response to tumors, recent therapies that have been developed to exploit these interactions and the role of predictive biomarkers in treatment selection. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:101 / 109
页数:9
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