From clonal hematopoiesis to myeloid leukemia and what happens in between: Will improved understanding lead to new therapeutic and preventive opportunities?

CCUS CHIP Clonal hematopoiesis Genetic testing ICUS Myeloid neoplasm

Journal

Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558

Informations de publication

Date de publication:
09 2019
Historique:
received: 10 02 2019
revised: 22 06 2019
accepted: 02 07 2019
pubmed: 12 8 2019
medline: 25 1 2020
entrez: 12 8 2019
Statut: ppublish

Résumé

Clonal hematopoiesis (CH) as defined by the presence of somatic mutations in genes associated with myeloid neoplasms (MN) is common in healthy elderly individuals and does not necessarily constitute a premalignant state. Several acronyms (idiopathic cytopenia of undetermined significance [ICUS], clonal cytopenia of undetermined significance [CCUS], CH of indeterminate potential [CHIP]) related to CH have been coined to describe patients who do not meet the diagnostic criteria for other hematologic disorders. CHIP carries an annual progression rate to MN of 0.5-1.0% as well as an increased risk of cardiovascular mortality and development of therapy-related MN in patients with solid tumors. Further studies on the natural history of ICUS, CCUS, and CHIP and to assess the risk for progression to MN are needed. Herein, we review the current understanding and clinical significance of these conditions to guide physicians in the interpretation of genetic testing results in various clinical settings.

Identifiants

pubmed: 31400824
pii: S0268-960X(19)30012-8
doi: 10.1016/j.blre.2019.100587
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

100587

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK102792
Pays : United States

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

Jan Philipp Bewersdorf (JP)

Section of Hematology, Department of Internal Medicine, Yale University School of Medicine and Yale Comprehensive Cancer Center, New Haven, USA.

Anastasia Ardasheva (A)

Section of Hematology, Department of Internal Medicine, Yale University School of Medicine and Yale Comprehensive Cancer Center, New Haven, USA.

Nikolai A Podoltsev (NA)

Section of Hematology, Department of Internal Medicine, Yale University School of Medicine and Yale Comprehensive Cancer Center, New Haven, USA.

Abhay Singh (A)

State University at Buffalo-Jacobs School of Medicine and Biomedical Sciences, Roswell Park Comprehensive Cancer Center, Buffalo, USA.

Giulia Biancon (G)

Section of Hematology, Department of Internal Medicine, Yale University School of Medicine and Yale Comprehensive Cancer Center, New Haven, USA.

Stephanie Halene (S)

Section of Hematology, Department of Internal Medicine, Yale University School of Medicine and Yale Comprehensive Cancer Center, New Haven, USA; Yale Stem Cell Center and Yale RNA Center, Yale University School of Medicine, New Haven, USA.

Amer M Zeidan (AM)

Section of Hematology, Department of Internal Medicine, Yale University School of Medicine and Yale Comprehensive Cancer Center, New Haven, USA. Electronic address: amer.zeidan@yale.edu.

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Classifications MeSH