医学
嵌合抗原受体
细胞疗法
细胞因子释放综合征
汽车T细胞治疗
淋巴瘤
单采
T细胞
免疫疗法
肿瘤科
癌症
免疫学
细胞
内科学
免疫系统
血小板
遗传学
生物
作者
Leila Amini,Sara Silbert,Shannon L. Maude,Loretta J. Nastoupil,Carlos A. Ramos,Renier J. Brentjens,Craig S. Sauter,Nirali N. Shah,Mohamed Abou‐El‐Enein
标识
DOI:10.1038/s41571-022-00607-3
摘要
Chimeric antigen receptor (CAR) T cells have emerged as a potent therapeutic approach for patients with certain haematological cancers, with multiple CAR T cell products currently approved by the FDA for those with relapsed and/or refractory B cell malignancies. However, in order to derive the desired level of effectiveness, patients need to successfully receive the CAR T cell infusion in a timely fashion. This process entails apheresis of the patient’s T cells, followed by CAR T cell manufacture. While awaiting infusion at an authorized treatment centre, patients may receive interim disease-directed therapy. Most patients will also receive a course of pre-CAR T cell lymphodepletion, which has emerged as an important factor in enabling durable responses. The time between apheresis and CAR T cell infusion is often not a simple journey, with each milestone being a critical step that can have important downstream consequences for the ability to receive the infusion and the strength of clinical responses. In this Review, we provide a summary of the many considerations for preparing patients with B cell non-Hodgkin lymphoma or acute lymphoblastic leukaemia for CAR T cell therapy, and outline current limitations and areas for future research.
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