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ZUMA-3 中接受 brexucabtagene autoleucel 治疗的复发/难治性 B 细胞急性淋巴细胞白血病成人患者的 3 年分析

英文原题:Three-year analysis of adult patients with relapsed or refractory B-cell acute lymphoblastic leukemia treated with brexucabtagene autoleucel in ZUMA-3.

查看英文原题

Three-year analysis of adult patients with relapsed or refractory B-cell acute lymphoblastic leukemia treated with brexucabtagene autoleucel in ZUMA-3.

PubMed 2025/03/19(内容时间) Leukemia Q1 · IF 8.8(JCR 2025)

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中文摘要

Brexucabtagene autoleucel(brexu-cel)是一种自体抗 CD19 CAR-T 疗法,在美国获批用于治疗成人复发/难治性(R/R)B 急性淋巴细胞白血病(B-ALL)患者;年龄范围为 18 岁及以上(欧盟为 26 岁及以上)。在 ZUMA-3 研究中,78 例 R/R B-ALL 患者接受治疗并随访 2 年后,brexu-cel 的总体完全缓解(CR)/血液学恢复不完全的 CR(CRi)率为 73%(CR 率 60%),总生存期(OS)中位数为 25.4 个月。本文报告中位随访超过 3 年后的更新结局。

截至 2022 年 7 月 23 日,所有患者(N = 78)的中位随访时间为 41.6 个月。OS 中位数(95% CI)为 25.6 个月(1.2–47.0;N = 78);应答者(n = 58)为 38.9 个月(25.4–无法估计),其中 9 例患者在未接受后续治疗的情况下持续缓解。自上一次数据截止后又发生 5 例死亡(均未被认为与 brexu-cel 有关)。无论年龄、既往治疗或后续异基因干细胞移植(alloSCT)情况如何,brexu-cel 获益均得以维持。在应答者中,与未接受后续 alloSCT 的应答者相比,接受后续 alloSCT 未显示生存获益。ZUMA-3 长期随访未报告继发性 T 细胞恶性肿瘤。

展开英文摘要原文

Brexucabtagene autoleucel (brexu-cel) is an autologous anti-CD19 CAR T-cell therapy approved in the US to treat adults aged 18 years ( 26 years in the EU) with relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL). Brexu-cel showed an overall complete remission (CR)/CR with incomplete hematologic recovery (CRi) rate of 73% (CR rate 60%) and median overall survival (OS) of 25. 4 months in 78 patients with R/R B-ALL after 2 years in ZUMA-3.

Here, we report updated outcomes after >3 years median follow-up. As of July 23, 2022, median follow-up in all patients (N = 78) was 41. 6 months. Median OS (95% CI) was 25. 6 months (1. 2-47. 0; N = 78) and was 38. 9 months (25. 4-not estimable) for responders (n = 58), with 9 patients in ongoing remission without subsequent therapies. Five deaths (none deemed brexu-cel-related) occurred since prior data cut.

Benefits from brexu-cel were maintained regardless of age, prior therapies, and subsequent allogeneic stem cell transplantation (alloSCT). Subsequent alloSCT was not associated with survival benefit among responders versus responders without subsequent alloSCT. No secondary T-cell malignancies were reported in ZUMA-3 with long-term follow-up.

论文信息

作者
Shah BD、Cassaday RD、Park JH、Houot R、Logan AC、Boissel N、Leguay T、Bishop MR
单位
Moffitt Cancer Center, Tampa, FL, USA. bijal.shah@moffitt.org.United States
期刊
Leukemia2025 May
原文标识
PubMed 40108332 · DOI 10.1038/s41375-025-02532-7