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ZUMA-3 中 KTE-X19 治疗复发/难治性成人 B 细胞急性淋巴细胞白血病患者的 2 年随访及其与外部历史对照研究 SCHOLAR-3 的比较

英文原题:Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study.

查看英文原题

Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study.

PubMed 2022/12/10(内容时间) J Hematol Oncol Q1 · IF 47.8(JCR 2025)

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研究概要

这些数据代表了成人 R/R B-ALL 多中心研究中 CAR-T 细胞治疗的最长随访,表明 KTE-X19 在该人群中提供了具有临床意义的生存获益,且毒性可控。

研究思路结论见上方概要

Brexucabtagene autoleucel (KTE-X19) 是一种自体抗 CD19 CAR-T 细胞疗法,基于 ZUMA-3 研究结果,已在美国获批用于治疗复发/难治性 B 前体急性淋巴细胞白血病 (R/R B-ALL) 成人患者。我们报告了 ZUMA-3 的更新结局,随访时间更长,数据集扩大,并将结局与历史标准治疗进行背景化对比。

复发/难治性B-ALL成人患者接受单次KTE-X19输注(1×10^6 CAR-T 细胞/kg)。对ZUMA-3进行了长期事后亚组评估。在回顾性历史对照研究SCHOLAR-3中,评估了历史临床试验与ZUMA-3患者之间匹配患者的结局。

中位随访26.8个月后,2期治疗患者(N = 55)的总体完全缓解(CR)率(CR + 伴血液学恢复不完全的CR)为71%(CR率为56%);缓解持续时间和总生存期(OS)的中位数分别为14.6个月和25.4个月。大多数患者对KTE-X19有应答,无论年龄或基线骨髓原始细胞百分比如何,但原始细胞> 75%的患者应答较少。未观察到新的安全性信号。在1期和2期患者的汇总分析(N = 78)中观察到相似的结果。在SCHOLAR-3中,来自ZUMA-3的治疗患者(N = 49)和匹配的历史对照(N = 40)的中位OS分别为25.4个月和5.5个月。

展开英文摘要原文

Brexucabtagene autoleucel (KTE-X19) is an autologous anti-CD19 CAR T-cell therapy approved in the USA to treat adult patients with relapsed or refractory B-precursor acute lymphoblastic leukemia (R/R B-ALL) based on ZUMA-3 study results. We report updated ZUMA-3 outcomes with longer follow-up and an extended data set along with contextualization of outcomes to historical standard of care.

Adults with R/R B-ALL received a single infusion of KTE-X19 (1 10 6 CAR T cells/kg). Long-term post hoc subgroup assessments of ZUMA-3 were conducted. Outcomes from matched patients between historical clinical trials and ZUMA-3 patients were assessed in the retrospective historical control study SCHOLAR-3.

After 26.8-months median follow-up, the overall complete remission (CR) rate (CR + CR with incomplete hematological recovery) among treated patients (N = 55) in phase 2 was 71% (56% CR rate); medians for duration of remission and overall survival (OS) were 14.6 and 25.4 months, respectively. Most patients responded to KTE-X19 regardless of age or baseline bone marrow blast percentage, but less so in patients with > 75% blasts. No new safety signals were observed. Similar outcomes were observed in a pooled analysis of phase 1 and 2 patients (N = 78). In SCHOLAR-3, the median OS for treated patients from ZUMA-3 (N = 49) and matched historical controls (N = 40) was 25.4 and 5.5 months, respectively.

These data, representing the longest follow-up of CAR T-cell therapy in a multicenter study of adult R/R B-ALL, suggest that KTE-X19 provides a clinically meaningful survival benefit with manageable toxicity in this population. TRIAL REGISTRATION: NCT02614066.

论文信息

作者
Shah BD、Ghobadi A、Oluwole OO、Logan AC、Boissel N、Cassaday RD、Leguay T、Bishop MR
单位
Moffitt Cancer Center, Tampa, FL, 33612, USA. bijal.shah@moffitt.org.United States
文献类型
多中心研究
期刊
Journal of hematology & oncology2022 Dec 10
原文标识
PubMed 36494725 · DOI 10.1186/s13045-022-01379-0