| Literature DB >> 29330221 |
Gerrit J Schuurhuis1, Michael Heuser2, Sylvie Freeman3, Marie-Christine Béné4, Francesco Buccisano5, Jacqueline Cloos1,6, David Grimwade7, Torsten Haferlach8, Robert K Hills9, Christopher S Hourigan10, Jeffrey L Jorgensen11, Wolfgang Kern8, Francis Lacombe12, Luca Maurillo5, Claude Preudhomme13, Bert A van der Reijden14, Christian Thiede15, Adriano Venditti5, Paresh Vyas16, Brent L Wood17,18, Roland B Walter17,19, Konstanze Döhner20, Gail J Roboz21, Gert J Ossenkoppele1.
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.Entities:
Mesh:
Year: 2018 PMID: 29330221 PMCID: PMC5865231 DOI: 10.1182/blood-2017-09-801498
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476