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: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.
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.
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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。
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。
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.
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