From the Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY.
Cancer J. 2021;27(2):126-133. doi: 10.1097/PPO.0000000000000507.
Chimeric antigen receptor (CAR) T-cell therapy is a highly effective new treatment for relapsed and refractory hematological cancers but is associated with the novel treatment-limiting toxicities of cytokine release syndrome and neurotoxicity. Neurotoxicity, now more commonly referred to as immune effector cell-associated neurotoxicity syndrome (ICANS), is a clinical and neuropsychiatric syndrome that can occur in the days to weeks following CAR T-cell and other T-cell-engaging therapies. While the clinical characteristics of ICANS have been well described, its pathophysiology is poorly understood, and best treatment and preventive strategies remain elusive. Clinical trial experience and animal models suggest a central role for endothelial cell dysfunction, myeloid cells, blood-brain barrier disruption, and elevated central nervous system cytokine levels in the development of ICANS. Here we discuss ICANS incidence, clinical features, risk factors, biomarkers, pathophysiology, and grading and management.
嵌合抗原受体 (CAR) T 细胞疗法是一种治疗复发和难治性血液系统癌症的高效新方法,但与细胞因子释放综合征和神经毒性等新型治疗限制毒性有关。神经毒性,现在更常被称为免疫效应细胞相关神经毒性综合征 (ICANS),是一种在 CAR T 细胞和其他 T 细胞参与的治疗后数天至数周内发生的临床和神经精神综合征。虽然已经很好地描述了 ICANS 的临床特征,但它的病理生理学仍不清楚,最佳的治疗和预防策略仍难以捉摸。临床试验经验和动物模型表明,内皮细胞功能障碍、髓样细胞、血脑屏障破坏和中枢神经系统细胞因子水平升高在 ICANS 的发展中起核心作用。在这里,我们讨论了 ICANS 的发病率、临床特征、危险因素、生物标志物、病理生理学以及分级和管理。