Hay Kevin A, Turtle Cameron J
Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Clinical Research Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave., Seattle, WA, 98109, USA.
Drugs. 2017 Mar;77(3):237-245. doi: 10.1007/s40265-017-0690-8.
Adoptive immunotherapy with chimeric antigen receptor-modified (CAR)-T cells is a rapidly growing therapeutic approach to treating patients with refractory cancer, with over 100 clinical trials in various malignancies in progress. The enthusiasm for CAR-T cells has been driven by the clinical success of CD19-targeted CAR-T cell therapy in B-cell acute lymphoblastic leukemia, and the promising data in B-cell non-Hodgkin's lymphoma and chronic lymphocytic leukemia. Despite the success of targeting CD19 with CAR-T cells in early clinical studies, many challenges remain to improve outcomes, reduce toxicity, and determine the appropriate settings for CAR-T cell immunotherapy. Reviewing the lessons learned thus far in CD19 CAR-T cell trials and how some of these challenges may be overcome will help guide the development of CAR-T cell therapy for malignancies of B-cell origin, as well as for other hematopoietic and non-hematopoietic cancers.
嵌合抗原受体修饰(CAR)-T细胞过继性免疫疗法是一种发展迅速的治疗难治性癌症患者的方法,目前有100多项针对各种恶性肿瘤的临床试验正在进行。靶向CD19的CAR-T细胞疗法在B细胞急性淋巴细胞白血病中的临床成功,以及在B细胞非霍奇金淋巴瘤和慢性淋巴细胞白血病中获得的有前景的数据,推动了人们对CAR-T细胞的热情。尽管在早期临床研究中,CAR-T细胞靶向CD19取得了成功,但仍有许多挑战需要应对,以改善治疗效果、降低毒性,并确定CAR-T细胞免疫疗法的合适应用场景。回顾迄今为止在CD19 CAR-T细胞试验中吸取的经验教训,以及如何克服其中一些挑战,将有助于指导针对B细胞起源的恶性肿瘤以及其他血液系统和非血液系统癌症的CAR-T细胞疗法的发展。
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