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:Anti-CD19 chimeric antigen receptor (CAR)-T cell therapy vs. CD20xCD3 bispecific antibody as third- or later-line treatment in follicular lymphoma: a meta-analysis.
Anti-CD19 chimeric antigen receptor (CAR)-T cell therapy vs. CD20xCD3 bispecific antibody as third- or later-line treatment in follicular lymphoma: a meta-analysis.
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抗CD19嵌合抗原受体(CAR)-T细胞疗法和CD20xCD3双特异性抗体(BsAbs)均被推荐为滤泡性淋巴瘤(FL)三线及后续治疗的优选方案。
我们旨在比较CAR-T 和BsAbs在复发/难治性(R/R)FL三线或更后线治疗中的疗效和安全性。我们检索了PubMed、Embase和Cochrane Library数据库中截至2025年1月31日的试验。主要终点为总缓解率(ORR)。次要终点包括完全缓解率(CRR)、12个月无进展生存期(PFS),以及细胞因子释放综合征(CRS)、神经毒性和感染相关的3级不良事件。本meta分析共纳入8项研究,包含725例在接受2线全身治疗后出现R/R疾病的1-3a级FL患者。CAR-T 的合并ORR为0.93(95% CI,0.84 0.97),BsAbs为0.81(95% CI,0.77 0.85)(P = 0.02)。在安全性方面,两组在3级CRS、神经毒性和感染方面未观察到显著差异。作为R/R FL的三线或更后线治疗,抗CD19 CAR-T 细胞疗法较CD20xCD3 BsAbs表现出更高的ORR,且毒性相当。注册号:PROSPERO 2025 CRD420251005804。
Both anti-CD19 chimeric antigen receptor (CAR)-T cell therapy and CD20xCD3 bispecific antibodies (BsAbs) are recommended as preferred regimens of third-line and subsequent treatment for follicular lymphoma (FL).
We aimed to compare the efficacy and safety of CAR-T and BsAbs in third- or later-line treatments for relapsed or refractory (R/R) FL.
We reviewed trials from PubMed, Embase and Cochrane Library databases up to January 31, 2025. Primary endpoint was overall response rate (ORR). Secondary endpoints included complete response rate (CRR), 12-month progression-free survival (PFS), and grade 3 adverse events of cytokine release syndrome (CRS), neurotoxicity, and infection. Eight studies comprising 725 grade 1-3a FL patients with R/R disease after 2 lines of systemic therapy were included in the meta-analysis.
The pooled ORR was 0. 93 (95% CI, 0. 84 0. 97) for CAR-T and 0. 81 (95% CI, 0. 77 0. 85) for BsAbs (P = 0. 02). For safety profiles, no significant difference was observed between the two groups in terms of grade 3 CRS, neurotoxicity, and infections. Anti-CD19 CAR-T cell therapy exhibited higher ORR compared to CD20xCD3 BsAbs as third- or later-line treatment for R/R FL with comparable toxicities. Registration: PROSPERO 2025 CRD420251005804.
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