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:Predictors of cytopenias after treatment with axicabtagene ciloleucel in patients with large B-cell lymphoma.
Predictors of cytopenias after treatment with axicabtagene ciloleucel in patients with large B-cell lymphoma.
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血细胞减少是嵌合抗原受体工程化T细胞(CAR-T)治疗后重要但研究较少的不良事件。本研究分析接受axicabtagene ciloleucel(axi-cel)治疗的大细胞淋巴瘤患者,旨在确定临床显著短期血细胞减少的发生率及危险因素。短期血细胞减少定义为axi-cel治疗后第20至30天发生3级中性粒细胞减少、贫血或血小板减少,或接受生长因子/血制品输注。研究期间53例患者接受axi-cel,其中32例(60%)出现重度血细胞减少。未应答者(疾病稳定或进展)的显著血细胞减少发生率高于应答者(部分或完全缓解)(100%比70%;p=0.01)。多变量模型显示,白细胞单采前一个月内输注血小板、单采至淋巴细胞清除期间红细胞和血小板输注次数、淋巴细胞清除前绝对中性粒细胞计数、淋巴细胞清除前乳酸脱氢酶水平,以及CAR-T 治疗后地塞米松使用次数,均与axi-cel治疗后重度血细胞减少显著相关。
Cytopenias are important but less studied adverse events following chimeric antigen receptor-engineered T cell (CAR-T) therapy. In our analysis of patients with large cell lymphoma who received axicabtagene ciloleucel (axi-cel), we sought to determine the rate and risk factors of clinically significant short term cytopenias defined as grade 3 neutropenia, anemia, or thrombocytopenia, or treatment with growth factors or blood product transfusions between days 20-30 after axi-cel. Fifty-three pts received axi-cel during the study period and severe cytopenias were observed in 32 (60%) pts.
Significant cytopenias were more common in non-responders (stable or progressive disease) vs. responders (partial or complete response) (100% vs. 70%; p = . 01). In the multivariable model, platelet transfusion within a month before leukapheresis, number of red blood cell and platelet transfusions between leukapheresis to lymphodepletion, pre-lymphodepletion absolute neurophil count, pre-lymphodepletion lactate dehydrogenase, and number of dexamethasone treatments after CAR-T were significantly associated with severe cytopenias after axi-cel.
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