GVHD prophylaxis after cord blood transplantation in patients with high-risk AML: a nationwide Japanese cohort study.
코호트
3/5 보강
TL;DR
MMF led to faster engraftment but higher GVHD than MTX in CBT for high-risk AML, suggesting benchmarks for individualized GVHD prevention strategies.
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
환자: high-risk acute myeloid leukemia (AML), including therapy-related AML (t-AML)
I · Intervention 중재 / 시술
their first CBT in Japan between 2010 and 2023
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Although MMF accelerates engraftment, this benefit is offset by greater GVHD and viral complications. These real-world, nationwide data highlight the need to individualize GVHD prophylaxis based on patient and transplant characteristics and provide essential benchmarks for future multicenter prospective studies.
OpenAlex 토픽 ·
Hematopoietic Stem Cell Transplantation
Acute Myeloid Leukemia Research
Neutropenia and Cancer Infections
MMF led to faster engraftment but higher GVHD than MTX in CBT for high-risk AML, suggesting benchmarks for individualized GVHD prevention strategies.
- p-value P < .001
- 연구 설계 cohort study
APA
Satoshi Yamasaki, Masamitsu Yanada, et al. (2026). GVHD prophylaxis after cord blood transplantation in patients with high-risk AML: a nationwide Japanese cohort study.. Blood advances, 10(8), 2648-2660. https://doi.org/10.1182/bloodadvances.2025018626
MLA
Satoshi Yamasaki, et al.. "GVHD prophylaxis after cord blood transplantation in patients with high-risk AML: a nationwide Japanese cohort study.." Blood advances, vol. 10, no. 8, 2026, pp. 2648-2660.
PMID
41538306 ↗
Abstract 한글 요약
Cord blood transplantation (CBT) is a curative option for patients with high-risk acute myeloid leukemia (AML), including therapy-related AML (t-AML). However, the optimal prophylaxis for graft-versus-host disease (GVHD) remains unclear. We conducted a nationwide, retrospective cohort study including 3222 adults with high-risk AML (t-AML and non-t-AML) who underwent their first CBT in Japan between 2010 and 2023. GVHD prophylaxis consisted of cyclosporine or tacrolimus combined with mycophenolate mofetil (CSP/TAC + MMF) or methotrexate (CSP/TAC + MTX). MMF regimens were associated with faster neutrophil engraftment than MTX regimens (P < .001). However, CSP/TAC + MMF showed significantly higher incidences of grades 2 to 4 acute GVHD (P < .001) and chronic GVHD (P < .001). Two-year transplant-related mortality and relapse rates were 26 to 38% and 41 to 46%, respectively. Overall survival and disease-free survival at 2 years were higher with MTX than with MMF (P < .001 and P = .003, respectively), indicating a modest survival advantage for MTX. Multivariable analysis identified older age (≥55 years), male sex, Karnofsky performance status <80, higher hematopoietic cell transplantation-specific comorbidity index, and no remission at transplantation as adverse prognostic factors. Notably, MMF use was associated with an increased risk of human herpesvirus 6 encephalitis. Both CSP/TAC + MMF and CSP/TAC + MTX regimens support successful CBT in high-risk AML. Although MMF accelerates engraftment, this benefit is offset by greater GVHD and viral complications. These real-world, nationwide data highlight the need to individualize GVHD prophylaxis based on patient and transplant characteristics and provide essential benchmarks for future multicenter prospective studies.
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