Applying molecular measurable residual disease testing in acute myeloid leukaemia.


Journal

Pathology
ISSN: 1465-3931
Titre abrégé: Pathology
Pays: England
ID NLM: 0175411

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 29 09 2022
revised: 12 11 2022
accepted: 14 11 2022
pubmed: 13 12 2022
medline: 11 1 2023
entrez: 12 12 2022
Statut: ppublish

Résumé

Molecular testing in acute myeloid leukaemia (AML) has continued to dramatically advance in recent years, facilitating the ability to detect residual disease at exponentially lower levels. With the advent of the recently updated ELN consensus recommendations, there is increasing complexity to ordering and interpreting measurable residual disease (MRD) assays in AML. We outline the technology itself in conjunction with the relevant testing timepoints, clinically significant thresholds and potential prognostic and therapeutic significance of MRD testing for the major molecular targets in AML. This practical overview should assist haematologists in incorporating molecular MRD assays routinely into their personalised AML clinical management.

Identifiants

pubmed: 36503638
pii: S0031-3025(22)00312-9
doi: 10.1016/j.pathol.2022.11.003
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Informations de copyright

Copyright © 2022 Royal College of Pathologists of Australasia. Published by Elsevier B.V. All rights reserved.

Auteurs

Michael Krigstein (M)

Department of Haematology, St Vincent's Hospital, Sydney, NSW, Australia. Electronic address: michael.krigstein@health.nsw.gov.au.

Harry J Iland (HJ)

Department of Haematology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

Andrew H Wei (AH)

Department of Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Vic, Australia.

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Classifications MeSH