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:Cytopenias following anti-CD19 chimeric antigen receptor (CAR) T cell therapy: a systematic analysis for contributing factors.
Cytopenias following anti-CD19 chimeric antigen receptor (CAR) T cell therapy: a systematic analysis for contributing factors.
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中性粒细胞减少是 CAR-T 治疗后最常见的血细胞减少,无论是所有级别还是 3 级。CAR-T 治疗后血细胞减少的发生率受患者年龄、性别、疾病和既往治疗线数,以及 CAR-T 细胞的靶点和共刺激结构域,以及用于生产的病毒载体的影响。关键信息:中性粒细胞减少是 CAR-T 治疗后最常见的血细胞减少。患者的临床特征、CAR-T 细胞的设计和 CAR-T 治疗方案可影响 CAR-T 治疗后血细胞减少的发生。
血细胞减少是CAR-T 细胞输注后最常见的不良事件之一,影响生活质量,并可能导致危及生命的出血和感染。本研究旨在系统综述抗CD19 CAR-T 治疗后的血细胞减少,并进一步分析其影响因素。
于2022年5月8日系统检索了包括PubMed、MEDLINE、Embase和Cochrane在内的数据库。采用随机效应meta分析估计血细胞减少的发生率,并应用亚组分析探讨异质性。
本研究共纳入68项研究,涉及2950例患者。所有级别贫血、血小板减少、中性粒细胞减少、白细胞减少、淋巴细胞减少和发热性中性粒细胞减少的总体发生率分别为65%、55%、78%、62%、70%和27%,相应的3级或更严重血细胞减少分别为33%、31%、61%、45%、46%和21%。亚组分析显示,中位年龄较低、男性比例(<65%)和桥接治疗比例(<80%)较低的亚组以及既往治疗中位线数为3的亚组中,血细胞减少的发生率增加。在疾病和治疗靶点方面,血细胞减少在ALL患者和双靶点CAR-T 疗法(靶向CD19联合其他靶点)中更为常见。此外,由慢病毒载体制造的CAR-T 产品以及具有CD28共刺激结构域的产品更易引起血液学毒性。在接受鼠源和人源化scFv CAR-T 产品治疗的患者之间,血细胞减少未观察到显著差异。
Cytopenia is one of the most common adverse events following the CAR-T cell infusion, affecting the quality of life and potentially leading to life-threatening bleeding and infection. This study aimed to systematically review the cytopenias following anti-CD19 CAR-T therapy and further analyse the contributing factors.
Databases including PubMed, MEDLINE, Embase and Cochrane were systematically searched on 8 May 2022. A random-effect meta-analysis was used to estimate the incidence of cytopenia, and subgroup analyses were applied to explore heterogeneity.
A total of 68 studies involving 2950 patients were included in this study. The overall incidence of all grade anaemia, thrombocytopenia, neutropenia, leukopoenia, lymphocytopenia and febrile neutropenia was 65%, 55%, 78%, 62%, 70% and 27%, respectively, and the corresponding cytopenias of grade 3 or worse were 33%, 31%, 61%, 45%, 46%, and 21%, respectively. Subgroup analysis showed increased incidence of cytopenias in subgroups with lower median age, proportion of males (<65%) and proportion of bridging therapy (<80%) and in the subgroup with a median line of prior therapy 3. In terms of disease and therapeutic target, cytopenias were more frequent in ALL patients and in dual-target CAR-T therapies (targeting CD19 in combination with other targets). Furthermore, CAR-T products manufactured by lentiviral vectors and those with the costimulatory domain of CD28 were more likely to cause haematological toxicity. No significant differences were observed in cytopenia between patients treated with CAR-T products with murine and humanized scFv.
In conclusion, neutropenia is the most frequent cytopenia after CAR-T therapy, both in all grades or grade 3. The incidence of cytopenias following CAR-T therapy is influenced by the age, sex, disease and number of prior therapy lines of the patients, as well as the target and costimulatory domain of CAR-T cells, and viral vectors used for manufacturing.KEY MESSAGESNeutropenia is the most frequent cytopenia after CAR-T therapy.The clinical characteristics of the patients, the design of CAR-T cells and the protocol of CAR-T treatment can influence the occurrence of cytopenias following the CAR-T therapy.
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