Department of Medicine, Diakonie Hospital, Stuttgart, Germany.
Department of Neuropathology, University of Tübingen, Tübingen, Germany; and.
Blood Adv. 2021 Oct 12;5(19):3789-3793. doi: 10.1182/bloodadvances.2021004889.
Treatment with CD19-directed (CAR) T cells has evolved as a standard of care for multiply relapsed or refractory large B-cell lymphoma (r/r LBCL). A common side effect of this treatment is the immune effector cell-associated neurotoxicity syndrome (ICANS). Severe ICANS can occur in up to 30% to 40% of patients treated with axicabtagene-ciloleucel (axi-cel), usually within the first 4 weeks after administration of the dose and usually responding well to steroids. We describe a case of progressive central neurotoxicity occurring 9 months after axi-cel infusion in a patient with r/r LBCL who had undergone a prior allogeneic hematopoietic cell transplant. Despite extensive systemic and intrathecal immunosuppression, neurological deterioration was inexorable and eventually fatal within 5 months. High CAR T-cell DNA copy numbers and elevated levels of interleukin-1 (IL-1) and IL-6 were found in the cerebral spinal fluid as clinical symptoms emerged, and CAR T-cell brain infiltration was observed on autopsy, suggesting that CAR T cells played a major pathogenetic role. This case of unexpected, devastating, late neurotoxicity warrants intensified investigation of neurological off-target effects of CD19-directed CAR T cells and highlights the need for continuous monitoring for late toxicities in this vulnerable patient population.
嵌合抗原受体 T 细胞(CAR-T)治疗已发展成为复发性或难治性大 B 细胞淋巴瘤(r/r LBCL)的标准治疗方法。这种治疗的常见副作用是免疫效应细胞相关神经毒性综合征(ICANS)。接受 axicabtagene-ciloleucel(axi-cel)治疗的患者中,高达 30%至 40%可能会出现严重的 ICANS,通常在给药后 4 周内发生,且通常对类固醇反应良好。我们描述了一例 r/r LBCL 患者在接受 axi-cel 输注 9 个月后出现进行性中枢神经毒性的病例,该患者曾接受过异基因造血细胞移植。尽管进行了广泛的全身和鞘内免疫抑制治疗,但神经功能恶化仍不可避免,在 5 个月内最终导致死亡。在出现临床症状时,脑脊液中发现 CAR T 细胞 DNA 拷贝数升高和白细胞介素-1(IL-1)和白细胞介素-6(IL-6)水平升高,尸检观察到 CAR T 细胞脑浸润,提示 CAR T 细胞在发病机制中起主要作用。这种意料之外、严重、迟发性神经毒性的病例需要加强对 CD19 定向 CAR-T 细胞的神经毒性的非靶向作用的研究,并强调需要对这一脆弱患者群体的迟发性毒性进行持续监测。