Donor-derived CD7 CAR-T Cells for Pediatric and Adult Relapsed/Refractory T-ALL/LBL

2025.10.04
44
Blood

Publication Brief

Phase 2 trial establishing donor-derived CD7 CAR-T as a highly effective salvage therapy for both pediatric and adult patients with relapsed/refractory T-cell acute lymphoblastic leukemia/lymphoma.

Abstract

This phase 2 trial assessed CD7 chimeric antigen receptor (CAR) T cells derived  from previous transplant or newly HLA-matched donors for relapsed/refractory  T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL). Early termination from  departmental closure yielded 55 treated patients out of 70 planned. Within 3  months, 89% of treated patients achieved best overall response of partial  remission or better. A total of 19 received stem cell transplantation at a  median of 1.3 (range, 1.0-10.6) months. After a 26.3-month median follow-up,  median event-free survival was 5.0 months (95% confidence interval [4.1-8.4]),  with median 8.5-month overall survival (95% confidence interval [6.1-15.6]). No  deaths occurred within 30 days; adverse events included cytokine release  syndrome in 87% at grades 1 to 2 and 11% at grade 3 and neurotoxicity in 9% at  grade 1. In addition, graft-versus-host disease was in 38% at grades 1 to 2 and  2% at grade 3. Grades 1 and 2 infections occurred in 29%. Cytopenias occurred in  4% at grade 2 and 96% at grades 3 and 4. After 30 days, grades 3 to 5 adverse  events included cytopenias (grade 3 in 24%; grade 4 in 67%), infections (grade 3  in 9%; grade 4 in 5%; grade 5 in 9%), graft-versus-host disease (grade 3 in 4%;  grade 5 in 4%), thrombotic microangiopathy (grade 5 in 4%), and hepatic failure  (grade 5 in 2%). Furthermore, 11 encountered nonrelapse mortality after 30 days,  representing 20% of treated patients and 35% of responders without consolidatory  transplantation. Although effective at inducing remission, death in remission  beyond 30 days is a concern. This trial was registered at www.clinicaltrials.gov  as #NCT04689659.

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Journal: Blood. 2025 Dec 4.

Volume / Pages: 146(23):2745-2757

DOI: 10.1182/blood.2025029299

PubMed: PubMed: 40712157

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