Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italia.
Department of Neurology, IRCCS Humanitas Research Hospital, Milan, Italy.
J Neurol. 2023 May;270(5):2659-2673. doi: 10.1007/s00415-023-11595-4. Epub 2023 Mar 4.
To investigate neurotoxicity clinical and instrumental features, incidence, risk factors, and early and long-term prognosis in lymphoma patients who received CAR T-cell therapy.
In this prospective study, consecutive refractory B-cell non-Hodgkin lymphoma patients who received CAR T-cell therapy were included. Patients were comprehensively evaluated (neurological examination, EEG, brain MRI, and neuropsychological test) before and after (two and twelve months) CAR T-cells. From the day of CAR T-cells infusion, patients underwent daily neurological examinations to monitor the development of neurotoxicity.
Forty-six patients were included in the study. The median age was 56.5 years, and 13 (28%) were females. Seventeen patients (37%) developed neurotoxicity, characterized by encephalopathy frequently associated with language disturbances (65%) and frontal lobe dysfunction (65%). EEG and brain FDG-PET findings also supported a predominant frontal lobe involvement. The median time at onset and duration were five and eight days, respectively. Baseline EEG abnormalities predicted ICANS development in the multivariable analysis (OR 4.771; CI 1.081-21.048; p = 0.039). Notably, CRS was invariably present before or concomitant with neurotoxicity, and all patients who exhibited severe CRS (grade ≥ 3) developed neurotoxicity. Serum inflammatory markers were significantly higher in patients who developed neurotoxicity. A complete neurological resolution following corticosteroids and anti-cytokines monoclonal antibodies was reached in all patients treated, except for one patient developing a fatal fulminant cerebral edema. All surviving patients completed the 1-year follow-up, and no long-term neurotoxicity was observed.
In the first prospective Italian real-life study, we presented novel clinical and investigative insights into ICANS diagnosis, predictive factors, and prognosis.
研究接受嵌合抗原受体 T 细胞(CAR T)治疗的淋巴瘤患者的神经毒性的临床和仪器特征、发生率、危险因素以及早期和长期预后。
在这项前瞻性研究中,纳入了接受 CAR T 细胞治疗的连续难治性 B 细胞非霍奇金淋巴瘤患者。在接受 CAR T 细胞治疗前后(治疗后 2 个月和 12 个月)对患者进行全面评估(包括神经检查、脑电图、脑 MRI 和神经心理学测试)。从 CAR T 细胞输注的那天开始,患者每天接受神经检查以监测神经毒性的发展。
研究共纳入 46 例患者,中位年龄为 56.5 岁,13 例(28%)为女性。17 例(37%)患者发生神经毒性,表现为常伴有语言障碍(65%)和额叶功能障碍(65%)的脑病。脑电图和脑 FDG-PET 检查结果也支持主要累及额叶。发病中位时间和持续时间分别为 5 天和 8 天。基线脑电图异常在多变量分析中预测 ICANS 的发生(OR 4.771;95%CI 1.081-21.048;p=0.039)。值得注意的是,CRS 总是在神经毒性之前或同时出现,所有出现严重 CRS(等级≥3)的患者均发生神经毒性。发生神经毒性的患者血清炎症标志物明显升高。除 1 例患者发生致命性暴发性脑水肿外,所有接受治疗的患者均在皮质类固醇和抗细胞因子单克隆抗体治疗后完全缓解神经毒性。所有存活患者完成了 1 年的随访,未观察到长期神经毒性。
在意大利首例前瞻性真实世界研究中,我们提出了关于 ICANS 诊断、预测因素和预后的新的临床和研究见解。