CAR T- cell therapy provides an opportunity for further consolidation treatment for relapsed or refractory adult Burkitt lymphoma patients

CAR-T细胞疗法为复发或难治性成人伯基特淋巴瘤患者提供了进一步巩固治疗的机会。

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Abstract

BACKGROUND: Relapsed or refractory (R/R) Burkitt lymphoma (BL) in adults is aggressive and lacks standardized salvage options. Data on the efficacy and safety of chimeric antigen receptor T (CAR-T) cell therapy in this population remains limited. METHODS: We retrospectively analyzed 25 adult patients with relapsed or refractory Burkitt lymphoma who received CAR T-cell therapy. Clinical data, treatment responses, and survival outcomes were collected from medical records. Bridging therapy and lymphodepleting regimens varied based on disease status. Treatment-related toxicities and CAR-T expansion were monitored. Primary endpoints included efficacy, safety, and survival. Risk factors associated with treatment outcomes were explored using univariate analyses. RESULTS: One month objective response rate (ORR) was 52%(13/25)(95%CI: 31.3-72.2), with a complete response rate (CRR) of 28% (7/25). Sixteen patients (64%) received sequential consolidation therapy including 9 who received a second CAR-T infusion, and 7 who proceeded to autologous or allogeneic hematopoietic stem cell transplantation. The median follow-up time was 26.10 months (range 14.50-57.17). The median OS was 5.49 months(95%CI 1.74-9.25), and the median PFS was 2.96(95%CI 1.62-4.3)months. At last follow-up(2024-08-22), 28% achieved disease-free survival, with one patient disease-free for 5 years. CONCLUSIONS: CAR-T therapy shows promising activity in relapsed/refractory Burkitt lymphoma, but its effectiveness is limited by short response duration. High-risk features may predict poor outcomes, and a higher number of long-term survivors were observed in patients who received transplant sequential consolidation. However, due to the small sample size, larger studies are needed to validate these findings.

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