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Acute Myeloid Leukemia Patients With Myelodysplasia-Related Gene Mutations Benefit From Post-Transplant Hypomethylating Agent Maintenance.

1/5 보강
Transplantation and cellular therapy 📖 저널 OA 26.4% 2025: 2/13 OA 2026: 22/78 OA 2025~2026 2025
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
469 patients ultimately included for analysis.
I · Intervention 중재 / 시술
allo-HSCT between January 2017 and April 2023 were screened, with 469 patients ultimately included for analysis
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Meta-analysis indicated that treatment efficacy across different centers was comparable. Our findings reported the specific subgroups of adverse-risk AML patients who might benefit from post-transplant HMA maintenance.

Huang J, Xia Y, Xiang M, Zhang R, Yang Y, Chen H, Dong C, Li S, Zhu J, Jin C, Wang L, Jiang C, Huo W, Pan Z, Ma Y, Lu H, Tian Z, Zhang Z, Zhang J, Chen C, Cao W, Shi W, Zhao Y, Chen J, Cao Y, Mo X, Hu X

📝 환자 설명용 한 줄

Relapse remains the major cause of mortality in adverse-risk acute myeloid leukemia (AML) patients receiving allogeneic hematopoietic stem cell transplantation (allo-HSCT).

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 표본수 (n) 136
  • p-value P < .001
  • p-value P = .026
  • 연구 설계 Meta-analysis

이 논문을 인용하기

↓ .bib ↓ .ris
APA Huang J, Xia Y, et al. (2025). Acute Myeloid Leukemia Patients With Myelodysplasia-Related Gene Mutations Benefit From Post-Transplant Hypomethylating Agent Maintenance.. Transplantation and cellular therapy. https://doi.org/10.1016/j.jtct.2025.12.951
MLA Huang J, et al.. "Acute Myeloid Leukemia Patients With Myelodysplasia-Related Gene Mutations Benefit From Post-Transplant Hypomethylating Agent Maintenance.." Transplantation and cellular therapy, 2025.
PMID 41423033 ↗

Abstract

Relapse remains the major cause of mortality in adverse-risk acute myeloid leukemia (AML) patients receiving allogeneic hematopoietic stem cell transplantation (allo-HSCT). Hypomethylating agent (HMA) maintenance is a strategy to prevent post-transplant relapse, but its value among different genetically defined subgroups is still controversial. The study was designed to evaluate the efficacy of HMA maintenance in adverse-risk AML. In this retrospective, multicenter study, consecutive adverse-risk AML patients who received allo-HSCT between January 2017 and April 2023 were screened, with 469 patients ultimately included for analysis. These patients were divided into a HMA maintenance treatment group (MT group, n = 136) and a nonmaintenance group (NMT group, n = 333). Adverse-risk patients transplanted in first complete remission (CR1) pre-HSCT had significantly better 3-year transplant outcomes compared to those in non-CR1. Baseline characteristics of patients in the MT and NMT groups were well balanced except for conditioning regimen, with more patients in the MT group receiving myeloablative conditioning (94.1% versus 76.0%, P < .001). HMA maintenance reduced the 3-year cumulative incidence of relapse (19.2% versus 34.0%, P = .026) and improved the 3-year probabilities of event-free survival (EFS) (68.6% versus 43.4%, P < .001), relapse-free survival (69.1% versus 48.6%, P = .001), and overall survival (72.1% versus 61.0%, P = .034). The benefit of HMA maintenance was most evident in AML patients with myelodysplasia-related gene mutations (e.g., for EFS, hazard ratio 0.47, P = .002), and those receiving allo-HSCT in first remission and with undetectable measurable residual disease might not benefit from this strategy. Meta-analysis indicated that treatment efficacy across different centers was comparable. Our findings reported the specific subgroups of adverse-risk AML patients who might benefit from post-transplant HMA maintenance.

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