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ZUMA-3研究中接受brexucabtagene autoleucel治疗的复发或难治性B细胞急性淋巴细胞白血病成年患者的三年分析

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

作者信息

Shah Bijal D, Cassaday Ryan D, Park Jae H, Houot Roch, Logan Aaron C, Boissel Nicolas, Leguay Thibaut, Bishop Michael R, Topp Max S, O'Dwyer Kristen M, Tzachanis Dimitrios, Arellano Martha L, Lin Yi, Baer Maria R, Schiller Gary J, Subklewe Marion, Abedi Mehrdad, Minnema Monique C, Wierda William G, DeAngelo Daniel J, Stiff Patrick, Jeyakumar Deepa, Mao Daqin, Adhikary Sabina, Zhou Lang, Hadjivassileva Tsveta, Damico Khalid Rita, Ghobadi Armin, Oluwole Olalekan O

机构信息

Moffitt Cancer Center, Tampa, FL, USA.

University of Washington & Fred Hutchinson Cancer Center, Seattle, WA, USA.

出版信息

Leukemia. 2025 May;39(5):1058-1068. doi: 10.1038/s41375-025-02532-7. Epub 2025 Mar 19.

Abstract

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.

摘要

布雷西尤卡布他赛(brexu-cel)是一种自体抗CD19嵌合抗原受体T细胞疗法,在美国被批准用于治疗年龄≥18岁(在欧盟为≥26岁)的复发/难治性(R/R)B细胞急性淋巴细胞白血病(B-ALL)成人患者。在ZUMA-3研究中,78例R/R B-ALL患者接受治疗2年后,布雷西尤卡布他赛显示总体完全缓解(CR)/伴有血液学不完全恢复的CR(CRi)率为73%(CR率60%),中位总生存期(OS)为25.4个月。在此,我们报告了中位随访超过3年后的更新结果。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。中位OS(95%CI)为25.6个月(1.2 - 47.0;N = 78),应答者(n = 58)的中位OS为38.9个月(25.4 - 不可估计),有9例患者持续缓解且未接受后续治疗。自上次数据截止以来发生了5例死亡(均认为与布雷西尤卡布他赛无关)。无论年龄、既往治疗以及后续异基因造血干细胞移植(alloSCT)情况如何,布雷西尤卡布他赛的益处均得以维持。与未进行后续alloSCT的应答者相比,后续alloSCT并未给应答者带来生存获益。在ZUMA-3研究的长期随访中,未报告继发性T细胞恶性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a2/12055586/cdeb95e9e492/41375_2025_2532_Fig1_HTML.jpg

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