Sharma Naman, Reagan Patrick M, Liesveld Jane L
Department of Hematology-Oncology, Baystate Medical Center, University of Massachusetts Medical School, Springfield, MA 100107, USA.
Department of Medicine, Hematology-Oncology, James P. Wilmot Cancer Institute, University of Rochester, Rochester, NY 14642, USA.
Cancers (Basel). 2022 Mar 15;14(6):1501. doi: 10.3390/cancers14061501.
Chimeric Antigen Receptor T-cell (CAR-T) immunotherapy has emerged as an efficacious and life extending treatment modality with high response rates and durable remissions in patients with relapsed and refractory non-Hodgkin lymphoma (NHL), follicular lymphoma, and B-cell acute lymphoblastic leukemia (B-ALL) as well as in other diseases. Prolonged or recurrent cytopenias after CAR-T therapy have increasingly been reported at varying rates, and the pathogenesis of this complication is not yet well-understood but is likely contributed to by multiple factors. Current studies reported are primarily retrospective, heterogeneous in terms of CAR-Ts used and diseases treated, non-uniform in definitions of cytopenias and durations for end points, and vary in terms of recommended management. Prospective studies and correlative laboratory studies investigating the pathophysiology of prolonged cytopenias will enhance our understanding of this phenomenon. This review summarizes knowledge of these cytopenias to date.
嵌合抗原受体T细胞(CAR-T)免疫疗法已成为一种有效的、延长生命的治疗方式,在复发难治性非霍奇金淋巴瘤(NHL)、滤泡性淋巴瘤、B细胞急性淋巴细胞白血病(B-ALL)以及其他疾病患者中具有高缓解率和持久缓解。越来越多的报告显示,CAR-T治疗后会出现不同程度的长期或复发性血细胞减少,这种并发症的发病机制尚未完全明确,但可能是多种因素共同作用的结果。目前报道的研究主要是回顾性的,在使用的CAR-T和治疗的疾病方面存在异质性,血细胞减少的定义和终点持续时间不统一,推荐的管理方法也各不相同。研究长期血细胞减少病理生理学的前瞻性研究和相关实验室研究将增进我们对这一现象的理解。本综述总结了迄今为止关于这些血细胞减少的知识。