Minimal/measurable residual disease in AML: a consensus document from the European LeukemiaNet MRD Working Party

Author:

Schuurhuis Gerrit J.1ORCID,Heuser Michael2,Freeman Sylvie3,Béné Marie-Christine4ORCID,Buccisano Francesco5ORCID,Cloos Jacqueline16ORCID,Grimwade David7,Haferlach Torsten8,Hills Robert K.9,Hourigan Christopher S.10ORCID,Jorgensen Jeffrey L.11,Kern Wolfgang8ORCID,Lacombe Francis12,Maurillo Luca5,Preudhomme Claude13,van der Reijden Bert A.14ORCID,Thiede Christian15ORCID,Venditti Adriano5ORCID,Vyas Paresh16,Wood Brent L.1718ORCID,Walter Roland B.1719ORCID,Döhner Konstanze20,Roboz Gail J.21,Ossenkoppele Gert J.1

Affiliation:

1. Department of Hematology, VU University Medical Center, Amsterdam, The Netherlands;

2. Department of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany;

3. Department of Clinical Immunology, Institute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom;

4. Hematology Biology, University Hospital Nantes, Nantes, France;

5. Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy;

6. Department of Pediatric Oncology, VU University Medical Center, Amsterdam, The Netherlands;

7. Division of Genetics & Molecular Medicine, King’s College, London, United Kingdom;

8. MLL Munich Leukemia Laboratory, Munich, Germany;

9. Centre for Trials Research, Cardiff University, Cardiff, United Kingdom;

10. Myeloid Malignancies Section, National Institutes of Health, Bethesda, MD;

11. Division of Pathology/Laboratory Medicine, Department of Hematopathology, MD Anderson Cancer Center, Houston, TX;

12. Flow Cytometry Platform, University Hospital, Bordeaux, France;

13. Center of Pathology, Laboratory of Hematology, University Hospital of Lille, Lille, France;

14. Department of Laboratory Medicine, Laboratory of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands;

15. Universitätsklinikum Carl Gustav Garus an der Technischen Universität Dresden, Dresden, Germany;

16. Medical Research Council Molecular Haematology Unit, Oxford Centre for Haematology, University of Oxford and Oxford University Hospitals National Health Service Trust, Oxford, United Kingdom;

17. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

18. Department of Laboratory Medicine and

19. Division of Hematology, Department of Medicine, University of Washington, Seattle, WA;

20. Department of Internal Medicine III, University Hospital of Ulm, Ulm, Germany; and

21. Weill Cornell Medicine and New York Presbyterian Hospital, New York, NY

Abstract

Abstract Measurable residual disease (MRD; previously termed minimal residual disease) is an independent, postdiagnosis, prognostic indicator in acute myeloid leukemia (AML) that is important for risk stratification and treatment planning, in conjunction with other well-established clinical, cytogenetic, and molecular data assessed at diagnosis. MRD can be evaluated using a variety of multiparameter flow cytometry and molecular protocols, but, to date, these approaches have not been qualitatively or quantitatively standardized, making their use in clinical practice challenging. The objective of this work was to identify key clinical and scientific issues in the measurement and application of MRD in AML, to achieve consensus on these issues, and to provide guidelines for the current and future use of MRD in clinical practice. The work was accomplished over 2 years, during 4 meetings by a specially designated MRD Working Party of the European LeukemiaNet. The group included 24 faculty with expertise in AML hematopathology, molecular diagnostics, clinical trials, and clinical medicine, from 19 institutions in Europe and the United States.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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