Department of Medical Oncology and Hematology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
J Immunother Cancer. 2023 Jan;11(1). doi: 10.1136/jitc-2022-006059.
Immune effector cell-associated neurotoxicity syndrome (ICANS) is a common adverse event of CD19-directed chimeric antigen receptor (CAR) T cell therapy. Other neurological adverse events, however, have not methodically been described and studied. Furthermore, safety data on CAR-T cell therapy in patients with central nervous system (CNS) lymphoma remain limited.
We here report occurrence of a Guillain-Barré-like syndrome (GBS) and central diabetes insipidus (cDI) following tisagenlecleucel therapy for relapsed high-grade lymphoma with CNS involvement. Both complications were refractory to standard treatment of ICANS. Weakness of respiratory muscles required mechanical ventilation and tracheostomy while cDI was treated with desmopressin substitution for several weeks. Muscle-nerve biopsy and nerve conduction studies confirmed an axonal pattern of nerve damage. T cell-rich infiltrates and detection of the CAR transgene in muscle-nerve sections imply a direct or indirect role of CAR-T cell-mediated inflammation. In line with current treatment guidelines for GBS, intravenous immunoglobulin was administered and gradual but incomplete recovery was observed over the course of several months.
This case report highlights the risk of rare but severe neurological adverse events, such as acute GBS or cDI, in patients treated with CAR-T cells. It further underlines the importance of appropriate patient surveillance and systematic reporting of rare complications to eventually improve treatment.
免疫效应细胞相关神经毒性综合征(ICANS)是 CD19 导向嵌合抗原受体(CAR)T 细胞治疗的常见不良反应。然而,其他神经系统不良事件尚未系统地描述和研究。此外,CAR-T 细胞治疗中枢神经系统(CNS)淋巴瘤患者的安全性数据仍然有限。
我们在此报告一例复发高级别伴 CNS 受累淋巴瘤患者在接受 tisagenlecleucel 治疗后发生格林-巴利样综合征(GBS)和中枢性尿崩症(cDI)。这两种并发症均对 ICANS 的标准治疗无效。呼吸肌无力需要机械通气和气管切开,而 cDI 则用去氨加压素替代治疗数周。肌肉神经活检和神经传导研究证实存在轴索性神经损伤。富含 T 细胞的浸润和肌肉神经切片中 CAR 转基因的检测提示 CAR-T 细胞介导的炎症具有直接或间接作用。根据 GBS 的现行治疗指南,给予了静脉注射免疫球蛋白,在几个月的时间里观察到逐渐但不完全的恢复。
本病例报告强调了接受 CAR-T 细胞治疗的患者存在罕见但严重的神经系统不良事件(如急性 GBS 或 cDI)的风险。它进一步强调了适当的患者监测和对罕见并发症的系统报告的重要性,最终可以改善治疗。