Author:
Shah Bijal D.,Ghobadi Armin,Oluwole Olalekan O.,Logan Aaron C.,Boissel Nicolas,Cassaday Ryan D.,Leguay Thibaut,Bishop Michael R.,Topp Max S.,Tzachanis Dimitrios,O’Dwyer Kristen M.,Arellano Martha L.,Lin Yi,Baer Maria R.,Schiller Gary J.,Park Jae H.,Subklewe Marion,Abedi Mehrdad,Minnema Monique C.,Wierda William G.,DeAngelo Daniel J.,Stiff Patrick,Jeyakumar Deepa,Dong Jinghui,Adhikary Sabina,Zhou Lang,Schuberth Petra C.,Faghmous Imi,Masouleh Behzad Kharabi,Houot Roch
Abstract
Abstract
Background
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.
Methods
Adults with R/R B-ALL received a single infusion of KTE-X19 (1 × 106 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.
Results
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.
Conclusions
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.
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology,Molecular Biology,Hematology
Cited by
38 articles.
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