Ferreri Christopher J, Bhutani Manisha
Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health Wake Forest University School of Medicine, Charlotte, NC, United States.
Front Oncol. 2024 May 21;14:1396490. doi: 10.3389/fonc.2024.1396490. eCollection 2024.
Chimeric antigen receptor (CAR) T cell therapies have dramatically improved treatment outcomes for patients with relapsed or refractory B-cell acute lymphoblastic leukemia, large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, and multiple myeloma. Despite unprecedented efficacy, treatment with CAR T cell therapies can cause a multitude of adverse effects which require monitoring and management at specialized centers and contribute to morbidity and non-relapse mortality. Such toxicities include cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, neurotoxicity distinct from ICANS, immune effector cell-associated hemophagocytic lymphohistiocytosis-like syndrome, and immune effector cell-associated hematotoxicity that can lead to prolonged cytopenias and infectious complications. This review will discuss the current understanding of the underlying pathophysiologic mechanisms and provide guidelines for the grading and management of such toxicities.
嵌合抗原受体(CAR)T细胞疗法显著改善了复发或难治性B细胞急性淋巴细胞白血病、大B细胞淋巴瘤、滤泡性淋巴瘤、套细胞淋巴瘤和多发性骨髓瘤患者的治疗结果。尽管CAR T细胞疗法具有前所未有的疗效,但该疗法可能会导致多种不良反应,这些不良反应需要在专科中心进行监测和管理,并会导致发病率和非复发死亡率。此类毒性包括细胞因子释放综合征、免疫效应细胞相关神经毒性综合征、与免疫效应细胞相关噬血细胞性淋巴组织细胞增生症样综合征,以及可导致长期血细胞减少和感染并发症的免疫效应细胞相关血液毒性。本综述将讨论对潜在病理生理机制的当前认识,并提供此类毒性分级和管理的指南。