不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Neurological management and work-up of neurotoxicity associated with CAR T cell therapy.
Neurological management and work-up of neurotoxicity associated with CAR T cell therapy.
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在我们的队列中,ICANS 仅每 4 例患者中发生 1 例,且在每日检查中发现的神经毒性级别相当低。
本研究为单中心前瞻性观察研究,纳入汉诺威医学院一年内连续接受替沙仑赛治疗的15例r/r DLBCL患者。CAR-T 细胞输注前进行了全面的神经系统评估,包括临床检查、认知测试(蒙特利尔认知评估)、脑部MRI、脑电图、神经电图和脑脊液分析。输注后连续10天进行神经系统检查,此后至少每周评估一次。
15例患者中有4例(27%)在CAR-T 细胞输注后6天内(第4至第6天)发生ICANS。3例2级ICANS患者出现相似的神经系统症状,包括失用、表达性失语、定向障碍和幻觉;这些患者的脑部MRI均未见明显异常。3例患者接受地塞米松治疗后,临床症状均迅速缓解。比较CAR-T 细胞治疗前的基线参数,发生和未发生ICANS的患者之间没有差异。
在本队列中,约每四名患者中有一名发生ICANS,日常检查发现的神经毒性总体较轻。研究结果表明,规范的神经系统基线检查和密切监测有助于及早发现CAR-T 细胞相关神经毒性,并可能预防更高级别的神经毒性。
Single center, prospective observational study of fifteen consecutive r/r DLBCL patients treated with Tisagenlecleucel within 1 year at Hannover Medical School. Extensive neurological work-up prior to CAR T cell infusion included clinical examination, cognitive testing (Montreal-Cognitive-Assessment), brain MRI, electroencephalogram, electroneurography, and analysis of cerebrospinal fluid. After CAR T cell infusion, patients were neurologically examined for 10 consecutive days. Afterwards, all patients were assessed at least once a week.
ICANS occurred in 4/15 patients (27%) within 6 days (4-6 days) after CAR T cell infusion. Patients with ICANS grade 2 (n = 3) exhibited similar neurological symptoms including apraxia, expressive aphasia, disorientation, and hallucinations, while brain MRI was inconspicuous in either case. Treatment with dexamethasone rapidly resolved the clinical symptoms in all three patients. Regarding baseline parameters prior to CAR T cell treatment, patients with and without ICANS did not differ.
In our cohort, ICANS occurred in only every fourth patient and rather low grade neurotoxicity was found during daily examination. Our results demonstrate that a structured neurological baseline examination and close monitoring are helpful to detect CAR T cell related neurotoxicity already at an early stage and to potentially prevent higher grade neurotoxicity.
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