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Donor- and patient-derived interleukin 6 knockdown CD19-targeted chimeric antigen receptor T cells exhibit similar efficacy and safety in treating relapsed B-cell acute lymphoblastic leukemia patients after allogeneic hematopoietic stem cell transplantation.

Cytotherapy 2026 Vol.28(6) p. 102118

Sun T, Ma JF, Jia X, Xu SZ, Liu SH, Lyu XY, Huang SM, Wu YJ, Yao Z, Qian CS, Li Z, Yu L, Dai HP, Gong WJ, Xue SL

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[BACKGROUND AIMS] Chimeric antigen receptor (CAR) T-cell therapy has significantly improved the prognosis of relapsed B-cell acute lymphoblastic leukemia (B-ALL) patients with recurrent disease after

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 18
  • p-value P = 0.061
  • p-value P = 0.0198

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APA Sun T, Ma JF, et al. (2026). Donor- and patient-derived interleukin 6 knockdown CD19-targeted chimeric antigen receptor T cells exhibit similar efficacy and safety in treating relapsed B-cell acute lymphoblastic leukemia patients after allogeneic hematopoietic stem cell transplantation.. Cytotherapy, 28(6), 102118. https://doi.org/10.1016/j.jcyt.2026.102118
MLA Sun T, et al.. "Donor- and patient-derived interleukin 6 knockdown CD19-targeted chimeric antigen receptor T cells exhibit similar efficacy and safety in treating relapsed B-cell acute lymphoblastic leukemia patients after allogeneic hematopoietic stem cell transplantation.." Cytotherapy, vol. 28, no. 6, 2026, pp. 102118.
PMID 41930803

Abstract

[BACKGROUND AIMS] Chimeric antigen receptor (CAR) T-cell therapy has significantly improved the prognosis of relapsed B-cell acute lymphoblastic leukemia (B-ALL) patients with recurrent disease after allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, whether to use donor- or patient-derived CAR T cells has not yet been clarified.

[METHODS] This was a retrospective analysis to compare the efficacy and safety of donor- and patient-derived super and safe CD19-targeted CAR T cells.

[RESULTS] No significant difference was found between the donor-derived (n = 18) and patient-derived (n = 16) CAR T-cell subgroups in terms of efficacy. Complete remission/complete remission with incomplete count recovery rate (94.4% versus 75.0%, P = 0.1642), duration of response (median, 633.0 versus 373.0 days, P = 0.8562), overall survival (median, 67.12 months versus undefined, P = 0.061) and event-free survival (median, 17.0 versus 12.42 months, P = 0.773) were comparable. With regard to safety, the incidence (55.6% versus 62.5%, P = 0.7385) and severity (P = 0.1802) of cytokine release syndrome were similar, as were the serum levels of interleukin 6 (median, 30.8 versus 40.0 pg/mL, P = 0.8329) and ferritin (median, 3788.6 versus 1781.3 μg/L, P = 0.3552). The incidence of acute graft-versus-host disease was significantly higher in the donor-derived super and safe CAR T-cell subgroup (33.33% versus 0.00%, P = 0.0198). The peak level of CAR T-cell amplification (median, 114 169 versus 316 000 copies, P = 0.2204) and the day reaching the peak (median, 9.5 versus 9.5 days, P = 0.8143) were both similar.

[CONCLUSIONS] B-ALL patients who relapse after allo-HSCT may benefit from either donor- or patient-derived CAR T-cell therapy, but the risk of graft-versus-host disease may be higher for donor-derived products.

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