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

Publication date

2022-12-10

Authors

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

Editors

Advisors

Supervisors

Document Type

Article

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cc_by

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 × 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. 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.

Keywords

Adult, Antigens, CD19/therapeutic use, Historically Controlled Study, Humans, Immunotherapy, Adoptive/methods, Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy, Receptors, Chimeric Antigen, Recurrence, Retrospective Studies, KTE-X19, ZUMA-3, CAR T-cell therapy, SCHOLAR-3, Brexucabtagene autoleucel, B-precursor acute lymphoblastic leukemia, Molecular Biology, Hematology, Oncology, Cancer Research, Multicenter Study, Journal Article

Citation

Shah, B D, Ghobadi, A, Oluwole, O O, Logan, A C, Boissel, N, Cassaday, R D, Leguay, T, Bishop, M R, Topp, M S, Tzachanis, D, O'Dwyer, K M, Arellano, M L, Lin, Y, Baer, M R, Schiller, G J, Park, J H, Subklewe, M, Abedi, M, Minnema, M C, Wierda, W G, DeAngelo, D J, Stiff, P, Jeyakumar, D, Dong, J, Adhikary, S, Zhou, L, Schuberth, P C, Faghmous, I, Masouleh, B K & Houot, R 2022, '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', Journal of hematology & oncology, vol. 15, no. 1, 170. https://doi.org/10.1186/s13045-022-01379-0