CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Long-term Neurologic Safety in Patients With B-Cell Lymphoma Treated With Anti-CD19 Chimeric Antigen Receptor T-Cell Therapy.
Long-term Neurologic Safety in Patients With B-Cell Lymphoma Treated With Anti-CD19 Chimeric Antigen Receptor T-Cell Therapy.
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在这组患者中,接受抗 CD19 CAR-T 细胞治疗 2 年后未观察到明显的神经认知或神经系统障碍。
抗CD19嵌合抗原受体(CAR)T细胞治疗是复发B细胞淋巴瘤的有前景疗法,但常伴急性神经毒性。其长期神经安全性尚未得到充分评估。
本中心连续收治的所有难治性淋巴瘤CAR-T 患者均接受神经系统检查、全面神经心理评估及脑部MRI(1例除外),并在基线时填写自评问卷。治疗2年仍无病的患者接受相同复评。所有神经评估均由资深神经科医生完成。
19例无病患者中,无人出现相较基线新增神经功能缺损或MRI改变。治疗前与2年后认知表现无差异,包括曾出现CAR-T 急性神经毒性的11例患者。自评问卷显示,32%的患者在2年时报告认知方面困扰,且总体稳定。与基线相比,治疗后2年医院焦虑抑郁量表(HADS)焦虑评分下降(中位数7/21比4/21,p=0.01)。 讨论:总之,该队列患者在抗CD19 CAR-T 治疗后2年未观察到显著神经认知或神经系统障碍。
Anti-CD19 chimeric antigen receptor (CAR) T-cell therapy is a promising treatment in relapsing B-cell lymphoma but is frequently associated with acute neurotoxicity. Neurologic long-term safety has not been thoroughly assessed.
All patients with consecutive refractory lymphoma admitted in our center for CAR T-cell therapy underwent neurologic examination, extensive neuropsychological assessment, and brain MRI (except 1 patient) and completed self-administrated questionnaires at baseline. The patients who remained disease-free at 2 years were re-evaluated similarly. All neurologic assessments were conducted by senior neurologists.
None of the 19 disease-free patients developed new neurologic deficits or MRI changes when compared with baseline. There was no difference in cognitive performances before and 2 years after, even for the 11 patients who had developed acute neurotoxicity after CAR T cells. In self-questionnaire assessments, cognitive complaint was stable, reported by 32% of the patients at 2 years. We observed a reduction in HADS anxiety scores 2 years after treatment when compared with baseline (median score: 7/21 vs 4/21, p = 0.01). DISCUSSION: In conclusion, no significant neurocognitive or neurologic disorders were observed in this cohort of patients, 2 years after treatment with anti-CD19 CAR T cells.
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