Novel immunotherapeutic drugs for the treatment of lung cancer

被引:15
|
作者
Peng, Ling [1 ]
Wang, Zibing [2 ,3 ]
Stebbing, Justin [4 ]
Yu, Zhentao [5 ,6 ]
机构
[1] Zhejiang Prov Peoples Hosp, Affiliated Peoples Hosp, Hangzhou Med Coll, Dept Resp Dis, Hangzhou, Zhejiang, Peoples R China
[2] Zhengzhou Univ, Affiliated Canc Hosp, Dept Immunotherapy, Zhengzhou, Henan, Peoples R China
[3] Henan Canc Hosp, Zhengzhou, Henan, Peoples R China
[4] Imperial Coll London, Dept Surg & Canc, Div Canc, London, England
[5] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, Dept Thorac Surg,Natl Canc Ctr, Shenzhen, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Shenzhen Hosp, Shenzhen, Peoples R China
关键词
cancer vaccine; immune checkpoint inhibitor; immunotherapy; lung cancer; tumor microenvironment; PATIENTS PTS; T-CELLS; ANTITUMOR; CHALLENGES; EFFICACY; VACCINES; NSCLC; TIM-3; VISTA; LAG-3;
D O I
10.1097/CCO.0000000000000800
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review Cancer cells evade immune surveillance partly due to the immunosuppressive features of the tumor microenvironment (TME). Currently approved immuno-oncology drugs for the treatment of lung cancer are aimed to inhibit immune checkpoints, such as programmed death protein-1 (PD-1), PD ligand-1 (PD-L1) and cytotoxic T lymphocyte-associated antigen 4. Despite these, researchers are currently racing to create the optimal cancer immunotherapy treatments. Recent findings Novel immunotherapeutic drugs mainly act on activated immune cells and exert their therapeutic effects by enhancing antitumor responses. In this article, we review new therapies for the treatment of lung cancer that enhance T cell priming, remove coinhibitory signals, supply costimulatory signals and condition the TME. As more immunotherapeutic targets are in studies, designing multimodal strategies to provide greater efficacy with lower toxicity will be necessary.
引用
收藏
页码:89 / 94
页数:6
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