Chimeric Antigen Receptor (CAR) T-Cell Therapy for Thoracic Malignancies

被引:72
|
作者
Kiesgen, Stefan [1 ]
Chicaybam, Leonardo [1 ]
Chintala, Navin K. [1 ]
Adusumilli, Prasad S. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Thorac Serv, 1275 York Ave, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Ctr Cell Engn, 1275 York Ave, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
T-cell therapy; Adoptive cell therapy; Immunotherapy; Thoracic cancers; LUNG-CANCER; MESOTHELIN OVEREXPRESSION; IMMUNE MICROENVIRONMENT; ADOPTIVE IMMUNOTHERAPY; METASTATIC MELANOMA; ANTITUMOR IMMUNITY; STROMAL CELLS; SOLID TUMORS; LYMPHOCYTES; CARCINOMA;
D O I
10.1016/j.jtho.2017.10.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chimeric antigen receptor (CAR) T cells are patient T cells that are transduced with genetically engineered synthetic receptors to target a cancer cell surface antigen. The remarkable clinical response rates achieved by adoptive transfer of T cells that target CD19 in patients with leukemia and lymphoma have led to a growing number of clinical trials exploring CAR T-cell therapy for solid tumors. Herein, we review the evolution of adoptive T-cell therapy; highlight advances in CAR T-cell therapy for thoracic malignancies; and summarize the targets being investigated in clinical trials for patients with lung cancer, malignant pleural mesothelioma, and esophageal cancer. We further discuss the barriers to successfully translating CAR T-cell therapy for solid tumors and present strategies that have been investigated to overcome these hurdles. (C) 2017 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 26
页数:11
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