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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Cognitive impairment in hematology patients planned for chimeric antigen receptor T-cell therapy.
Cognitive impairment in hematology patients planned for chimeric antigen receptor T-cell therapy.
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研究结果显示了广泛的认知和心理症状,强调了基线评估对于发现 CAR-T 后可能出现的认知症状的重要性。
CAR-T 细胞疗法用于治疗多种复发/难治性血液系统恶性肿瘤,并与认知方面的副作用相关。CAR-T 后认知障碍的准确诊断需要了解治疗前的基线认知状态。
晚期血液系统或实体器官恶性肿瘤的成年患者在接受CAR-T 前接受了认知评估,包括精神病理学和主观认知功能的自我报告问卷。一部分个体还完成了蒙特利尔认知评估(MoCA),以检验认知筛查的效用。
纳入的60例患者中,16例(27%)存在认知障碍,表现为六种独特的功能障碍模式。记忆障碍是最常见的发现(15%)。受损患者更可能患有B细胞急性淋巴细胞白血病(p = 0.024,BF 10 = 9.30)、更年轻(p = 0.007,BF 10 = 7.76)、有骨髓受累(p = 0.037,BF 10 = 5.18),或有精神病理学证据(p = 0.004,BF 10 = 31.30)。分析不支持认知筛查的效用。在完成精神病理学自评量表的患者中,九例(16%)在至少一个症状领域得分升高。
Chimeric antigen receptor T-cell (CAR-T) therapy is used to treat several types of relapsed and refractory hematological malignancies and is associated with cognitive side-effects. The accurate diagnosis of cognitive impairment following CAR-T requires knowledge of baseline cognitive status prior to the therapy. RESEARCH DESIGN AND METHODS: Adult patients with advanced hematologic or solid organ malignancies underwent cognitive assessment, including a self-report questionnaire of psychopathology and subjective cognitive function, prior to receiving CAR-T. A subset of individuals also completed the Montreal Cognitive Assessment (MoCA) to examine utility of cognitive screening.
Of 60 patients included, 16 (27%) had cognitive impairment, with six unique patterns of dysfunction. Memory impairment was the most common finding (15%). Impaired patients were more likely to have B-cell acute lymphoblastic leukemia ( p = 0.024, BF 10 = 9.30), be younger ( p = 0.007, BF 10 = 7.76), have bone marrow involvement ( p = 0.037, BF 10 = 5.18), or have evidence of psychopathology ( p = 0.004, BF 10 = 31.30). Analyses did not support the utility of cognitive screening. Of those patients who completed a self-report measure of psychopathology, nine (16%) were elevated on at least one symptom domain.
The findings demonstrate a broad spectrum of cognitive and psychological symptoms, emphasizing the importance of baseline evaluation for detecting cognitive symptoms that might arise after CAR-T.
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