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 endpoint in clinical trials. The 2025 update of the MRD guideline provides a comprehensive and refined framework for MRD assessment, aligned with the ELN 2022 genetic risk classification. Developed by members of the ELN-DAVID consortium, the guidelines incorporate expert consensus determined through a two-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 (UHS) NGS-based MRD assessment is now recommended for FLT3-ITD-mutated AML following intensive chemotherapy and prior to 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

Cloos, J., Valk, P., Thiede, C., Döhner, K., Roboz, G.j., Wood, B.l., et al. (2025). 2025 Update on MRD in Acute Myeloid Leukemia: A Consensus Document from the ELN-DAVID MRD Working Party. BLOOD, 147(11), 1147-1167 [10.1182/blood.2025031480].

2025 Update on MRD in Acute Myeloid Leukemia: A Consensus Document from the ELN-DAVID MRD Working Party

Venditti, Adriano
Validation
;
Buccisano, Francesco;
2025-12-15

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 endpoint in clinical trials. The 2025 update of the MRD guideline provides a comprehensive and refined framework for MRD assessment, aligned with the ELN 2022 genetic risk classification. Developed by members of the ELN-DAVID consortium, the guidelines incorporate expert consensus determined through a two-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 (UHS) NGS-based MRD assessment is now recommended for FLT3-ITD-mutated AML following intensive chemotherapy and prior to 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
15-dic-2025
Online ahead of print
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/15
Settore MEDS-09/B - Malattie del sangue
English
Con Impact Factor ISI
LAIP; DfN; AML; MRD; dPCR; NGS-FLT3; LAIP-based-DfN; MRD burden; Ultrahigh-sensitivity NGS; Qualitative MRD response
https://doi.org/10.1182/blood.2025031480
Cloos, J., Valk, P., Thiede, C., Döhner, K., Roboz, G.j., Wood, B.l., et al. (2025). 2025 Update on MRD in Acute Myeloid Leukemia: A Consensus Document from the ELN-DAVID MRD Working Party. BLOOD, 147(11), 1147-1167 [10.1182/blood.2025031480].
Cloos, J; Valk, Pjm; Thiede, C; Döhner, K; Roboz, Gj; Wood, Bl; Walter, Rb; Wang, Sa; Wierzbowska, A; Wei, Ah; Wu, D; Vergez, F; Venditti, A; Van Der...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/453544
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