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:Safety and efficacy of chimeric antigen receptor T-cell therapy for acute myeloid leukemia: A subgroup based meta-analysis.
Safety and efficacy of chimeric antigen receptor T-cell therapy for acute myeloid leukemia: A subgroup based meta-analysis.
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本荟萃分析强调了 CAR-T 细胞疗法在 AML 治疗中的潜力,尤其是与某些既往治疗和预处理方案联合时。
我们依据PRISMA指南,对多个数据库开展全面文献综述,聚焦CAR-T 细胞治疗AML的研究。纳入英文原创论文,排除非原创综述、摘要及非英语研究。采用Cochrane ROBINS-I工具评估偏倚风险。统计分析采用Cochrane Q检验和I²统计量进行荟萃分析,使用固定效应和随机效应模型,并评估发表偏倚。
检索纳入的研究共涉及57例接受CAR-T 细胞治疗的AML患者。荟萃分析显示CAR-T 治疗完全缓解率为48%,且不同研究设计、地点、既往移植史、预处理方案和CAR-T 来源亚组之间存在显著差异。中国患者、既往接受过造血细胞移植的患者,以及接受氟达拉滨和环磷酰胺预处理的患者完全缓解率最高。不良事件包括移植物抗宿主病(7%)和细胞因子释放综合征(53%)。
本荟萃分析凸显CAR-T 细胞治疗AML的潜力,尤其是在结合特定既往治疗和预处理方案时。结果提示,既往接受造血细胞移植及采用特定预处理方案的患者疗效可能更高。仍需开展更大规模随机试验以验证这些发现,并确立CAR-T 细胞疗法作为AML标准治疗的地位。
We conducted a comprehensive literature review across multiple databases, adhering to PRISMA guidelines and focusing on studies concerning CAR T-cell therapy in AML. We included original articles in English and excluded non-original reviews, abstracts, and non-English studies. The risk of bias was assessed using the Cochrane ROBINS-I tool. Statistical analysis involved meta-analysis with Cochrane's Q-test and I statistic, using both fixed-effect and random-effects models, and assessed for publication bias.
Our search yielded studies encompassing 57 AML patients treated with CAR T-cell therapy. The meta-analysis revealed a 48% incidence of complete remission with CAR T-cell therapy, varying significantly across subgroups based on study design, location, prior transplantation, conditioning regimen, and CAR T-cell source. The highest complete remission rates were observed in patients from China, those who had undergone prior hematopoietic cell transplantation, and those treated with fludarabine and cyclophosphamide conditioning regimen. Adverse events included graft-versus-host disease (7%) and cytokine release syndrome (53%).
This meta-analysis highlights the potential of CAR T-cell therapy in AML treatment, especially when integrated with certain prior treatments and conditioning regimens. The findings suggest a higher efficacy in patients with previous hematopoietic cell transplantation and specific conditioning regimens. Further large-scale, randomized trials are essential to confirm these findings and establish CAR T-cell therapy as a standard treatment for AML.
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