Measurable residual disease monitoring in AML: Prospects for therapeutic decision-making and new drug development

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Journal: American Journal of Hematology
Credit: 1.0 AMA PRA Category 1 CreditTM

Release Date: February 18, 2025

Abstract

Measurable residual disease (MRD) is strongly associated with risk of relapse and long-term survival outcomes in patients with acute myeloid leukemia (AML). Apart from its clear prognostic impact, MRD information is also increasingly used to guide therapeutic decision-making, including selection of appropriate patients for stem cell transplant, use of post-transplant maintenance, and candidacy for non-transplant maintenance therapies or MRD-directed clinical trials. While much progress has been made in accurately assessing MRD and understanding its clinical importance, many questions remain about how to optimize MRD testing and guide treatment decisions for individual patients. In this review, we discuss the common methods to assess MRD in AML and the prognostic impact of MRD across common clinical scenarios. We also review emerging and investigational strategies to target MRD and discuss some of the important unanswered questions and challenges in the field.

Activity Disclosures

The publication of this supplement has been funded by Abbvie Inc.

Nicholas J. Short has served as consultant for Pfizer Inc., GSK, NKARTA, Autolus, and Sanofi, reports receiving research grants from Takeda Oncology, Astellas Pharma Inc., Xencor, Stemline Therapeutics, Xencor, NextCure, and GSK, and has received honoraria from Amgen, Astellas Pharma Inc., Adaptive Biotechnologies, Novartis, Takeda Oncology, Pfizer Inc., Sanofi and BeiGene. Richard Dillon has served as a consultant for Astellas, Abbvie, Jazz, Pfizer and Servier and reports receiving research grants from Abbvie, Amgen, Pfizer and Jazz.

This activity underwent peer review in line with standards of editorial integrity and publication ethics. Conflicts of interest have been identified and resolved in accordance with John Wiley and Sons, Inc.’s Policy on Activity Disclosure and Conflict of Interest.

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John Wiley and Sons, Inc. is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. John Wiley and Sons, Inc. designates this journal-based CME activity for a maximum of 1.0 AMA PRA Category 1 Credit™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

For information on applicability and acceptance of continuing medical education credit for this activity, please consult your professional licensing board.

This activity is designed to be completed within 1 hour. To successfully earn credit, participants must complete the activity during the valid credit period, which is up to three years from initial publication. Additionally, a score of 70% or better is needed to pass the post test.

Link to content: American Journal of Hematology | Blood Research Journal | Wiley Online Library

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