Pediatric Oncology Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD, USA.
Seattle Children's Research Institute, Seattle, WA, USA.
Nat Rev Clin Oncol. 2021 Jun;18(6):363-378. doi: 10.1038/s41571-020-00456-y. Epub 2021 Jan 25.
As clinical advances with chimeric antigen receptor (CAR) T cells are increasingly described and the potential for extending their therapeutic benefit grows, optimizing the implementation of this therapeutic modality is imperative. The recognition and management of cytokine release syndrome (CRS) marked a milestone in this field; however, beyond the understanding gained in treating CRS, a host of additional toxicities and/or potential late effects of CAR T cell therapy warrant further investigation. A multicentre initiative involving experts in paediatric cell therapy, supportive care and/or study of late effects from cancer and haematopoietic stem cell transplantation was convened to facilitate the comprehensive study of extended CAR T cell-mediated toxicities and establish a framework for new systematic investigations of CAR T cell-related adverse events. Together, this group identified six key focus areas: extended monitoring of neurotoxicity and neurocognitive function, psychosocial considerations, infection and immune reconstitution, other end organ toxicities, evaluation of subsequent neoplasms, and strategies to optimize remission durability. Herein, we present the current understanding, gaps in knowledge and future directions of research addressing these CAR T cell-related outcomes. This systematic framework to study extended toxicities and optimization strategies will facilitate the translation of acquired experience and knowledge for optimal application of CAR T cell therapies.
随着嵌合抗原受体 (CAR) T 细胞的临床进展不断被描述,并且扩展其治疗效益的潜力不断增加,优化这种治疗方式的实施势在必行。细胞因子释放综合征 (CRS) 的识别和管理标志着该领域的一个里程碑;然而,除了在治疗 CRS 方面获得的认识之外,CAR T 细胞治疗的一系列其他毒性和/或潜在的迟发性效应需要进一步研究。一项涉及儿科细胞治疗、支持性护理和/或癌症和造血干细胞移植迟发效应研究专家的多中心倡议被召集起来,以促进对扩展的 CAR T 细胞介导的毒性的全面研究,并建立一个新的 CAR T 细胞相关不良事件系统研究的框架。该小组共同确定了六个重点关注领域:神经毒性和神经认知功能的扩展监测、社会心理考虑因素、感染和免疫重建、其他终末器官毒性、继发肿瘤的评估,以及优化缓解持续时间的策略。在此,我们介绍了针对这些 CAR T 细胞相关结果的当前认识、知识空白和未来研究方向。这个研究扩展毒性和优化策略的系统框架将促进所获得的经验和知识的转化,以实现 CAR T 细胞治疗的最佳应用。