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Clinical outcomes of modified busulfan plus cyclophosphamide versus total body irradiation plus cyclophosphamide for T-cell acute lymphoblastic leukemia/lymphoma.

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Leukemia & lymphoma 📖 저널 OA 8.7% 2022: 1/1 OA 2025: 2/55 OA 2026: 14/137 OA 2022~2026 2026 Vol.67(3) p. 685-698
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유사 논문
P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
Clinical outcomes of modified busulfan plus cyclophosphamide
C · Comparison 대조 / 비교
total body irradiation plus cyclophosphamide for T
O · Outcome 결과 / 결론
Among patients transplanted in first complete remission (CR1), outcomes were not significantly different between regimens. These findings suggest TBI-Cy may provide improved composite outcomes, mainly reflected by GRFS, and inform conditioning regimen selection in T-ALL/LBL.

Guo J, Li M, Zhang L, Zhang Q, Wang N, Wei Y

📝 환자 설명용 한 줄

T-cell acute lymphoblastic leukemia/lymphoblastic lymphoma (T-ALL/LBL) remains a challenging malignancy with poor prognosis.

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APA Guo J, Li M, et al. (2026). Clinical outcomes of modified busulfan plus cyclophosphamide versus total body irradiation plus cyclophosphamide for T-cell acute lymphoblastic leukemia/lymphoma.. Leukemia & lymphoma, 67(3), 685-698. https://doi.org/10.1080/10428194.2025.2605516
MLA Guo J, et al.. "Clinical outcomes of modified busulfan plus cyclophosphamide versus total body irradiation plus cyclophosphamide for T-cell acute lymphoblastic leukemia/lymphoma.." Leukemia & lymphoma, vol. 67, no. 3, 2026, pp. 685-698.
PMID 41489116 ↗

Abstract

T-cell acute lymphoblastic leukemia/lymphoblastic lymphoma (T-ALL/LBL) remains a challenging malignancy with poor prognosis. Allogeneic hematopoietic stem cell transplantation (allo-HCT) remains a key curative option, but the optimal conditioning regimen is unclear. We retrospectively analyzed 93 T-ALL/LBL patients undergoing allo-HCT between January 2010 and July 2023, including 72 with modified busulfan plus cyclophosphamide (mBuCy) and 21 with total body irradiation plus cyclophosphamide (TBI-Cy). Propensity score matching (PSM) was applied to adjust baseline differences. Prior to PSM, survival outcomes were not significantly different, though numerical trends favored TBI-Cy. After PSM, 3-year graft-versus-host disease-free, relapse-free survival (GRFS) was higher with TBI-Cy (52% vs. 22%;  = 0.036), while other endpoints remained comparable in terms of statistical significance. Among patients transplanted in first complete remission (CR1), outcomes were not significantly different between regimens. These findings suggest TBI-Cy may provide improved composite outcomes, mainly reflected by GRFS, and inform conditioning regimen selection in T-ALL/LBL.

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