医学
重症监护医学
微小残留病
肿瘤科
Blinatumoab公司
指南
髓系白血病
疾病
造血细胞
内科学
德尔菲法
造血干细胞移植
临床试验
协商一致会议
临床终点
米多司他林
髓样
梅德林
化疗方案
风险评估
白血病
诱导化疗
家庭医学
作者
Jacqueline Cloos,Peter J.M. Valk,Christian Thiede,Konstanze Döhner,Gail J. Roboz,Brent L. Wood,Roland B. Walter,Sa A. Wang,Agnieszka Wierzbowska,Andrew H. Wei,David Wu,François Vergez,Adriano Venditti,Bert A. van der Reijden,Arjan A. van de Loosdrecht,Ing Soo Tiong,Felicitas Thol,Marion Subklewe,Christophe Roumier,Tom Reuvekamp
出处
期刊:Blood
[Elsevier BV]
日期:2025-12-15
卷期号:147 (11): 1147-1167
被引量:15
标识
DOI:10.1182/blood.2025031480
摘要
ABSTRACT: Measurable residual disease (MRD) monitoring has become a critical component in the management of acute myeloid leukemia (AML), to inform prognosis, guide therapy, and serve as a key end point in clinical trials. The 2025 update of the MRD guideline provides a comprehensive and refined framework for MRD assessment, aligned with the European LeukemiaNet (ELN) 2022 genetic risk classification. Developed by members of the ELN AML MRD Working Party, the guidelines incorporate expert consensus determined through a 2-stage Delphi round. They address the clinical implementation of MRD methodologies, technical considerations, integration into clinical trials, and future directions. Importantly, MRD recommendations are tailored to individual prognostic and genetic subgroups. A new qualitative MRD response category, designated as optimal, warning, or high risk of treatment failure, has been introduced to facilitate contextual interpretation of the MRD burden and its clinical relevance. Notably, ultrahigh-sensitivity next-generation sequencing-based MRD assessment is now recommended for FLT3 internal tandem duplication-mutated AML after intensive chemotherapy and before allogeneic hematopoietic cell transplantation. A total of 56 recommendations were formulated, with 53 achieving a high level of consensus (≥90%). These updated guidelines represent a major step forward toward harmonizing MRD assessments in AML and enhancing its clinical utility across diverse treatment settings.
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