决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Persistent Cognitive Dysfunction After Chimeric Antigen Receptor T-Cell Therapy in Adolescents and Young Adults.
Persistent Cognitive Dysfunction After Chimeric Antigen Receptor T-Cell Therapy in Adolescents and Young Adults.
我们的病例发现表明,持续性认知功能障碍可能是青少年和年轻成人 B 细胞急性淋巴细胞白血病患者因 CAR-T 治疗所致神经毒性的一种潜在未被充分认识的结果。
背景:血液系统恶性肿瘤CAR-T治疗可引起神经系统并发症,即免疫效应细胞相关神经毒性综合征(ICANS),其神经认知病理仍未完全阐明。本研究旨在明确CAR-T潜在神经毒性所致的持续认知功能障碍。方法:本单中心连续病例研究纳入CAR-T治疗B细胞急性淋巴细胞白血病后发生ICANS的患者,在ICANS症状出现时评估认知功能,并随后于神经科随访。结果:2020至2022年接受CAR-T治疗的10例中,3例出现ICANS,均未发生癫痫。3例中的青春期前患者出现意识水平下降、震颤和纹状体体征,但无认知功能障碍。另2例青少年及年轻成人患者出现认知下降、短期和长期记忆丧失及情绪障碍。虽然免疫效应细胞相关脑病评分仍低,但两例认知损害均严重并致残。所有患者的神经系统状态均在1个月内完全恢复至CAR-T治疗前水平。结论:本病例系列提示,青少年及年轻成人B细胞急性淋巴细胞白血病患者接受CAR-T治疗后,持续认知功能障碍可能是一种尚未充分认识的神经毒性结局。开展详细神经心理评估可能有益。
BACKGROUND: Chimeric antigen receptor T-cell (CAR-T) therapy for hematological malignancies causes a neurological complication known as immune effector cell-associated neurotoxicity syndrome (ICANS). The precise neurocognitive pathology underlying ICANS remains incompletely described. The aim of this study is to elucidate that persistent cognitive dysfunction as potential neurotoxicity of CAR-T therapy. METHODS: This was a single-center consecutive study of ICANS caused by CAR-T therapy for B-cell acute lymphoblastic leukemia. We determined the cognitive functions of all patients with ICANS at the onset of ICANS symptoms and followed them up in the neurology department thereafter. RESULTS: Among the 10 CAR-T cases between 2020 and 2022, three patients had ICANS. None of the patients experienced seizures. Of the three patients, the preadolescent patient showed decreased levels of consciousness, tremors, and striatal signs without cognitive dysfunction. The other two adolescent and young adult patients presented with cognitive decline, short- and long-term memory loss, and emotional disturbances. Although the Immune Effector Cell-Associated Encephalopathy score remained low, the cognitive impairment was profound and disabling in both cases. The neurological status of all patients fully recovered to pre-CAR-T status within one month. CONCLUSIONS: The findings in our cases indicate that persistent cognitive dysfunction may be a potentially under-recognized outcome of neurotoxicity due to CAR-T therapy for B-cell acute lymphoblastic leukemia in adolescents and young adults. Detailed neuropsychologic assessments may be beneficial for CAR-T therapy.
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