SOHO State of the Art Updates and Next Questions: IDH Inhibition.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
09 2021
Historique:
received: 17 03 2021
revised: 23 04 2021
accepted: 03 05 2021
pubmed: 2 7 2021
medline: 9 2 2022
entrez: 1 7 2021
Statut: ppublish

Résumé

There has been extraordinary progress in the field of targeted therapy for myeloid malignancies in the last few years, especially due to the approval of various agents that can be used as monotherapy or in combination as first-line treatment or when facing a refractory or relapsed disease. Many successful trials have been conducted recently, and a consistent body of work about the efficacy of novel molecules is now available. In this review, we sought to explain how enasidenib and ivosidenib have changed the face of myeloid neoplasm treatment through isocitrate dehydrogenase inhibition and to summarize the trials results that have led to the current commercial indications for the two molecules.

Identifiants

pubmed: 34193376
pii: S2152-2650(21)00180-4
doi: 10.1016/j.clml.2021.05.004
pii:
doi:

Substances chimiques

Aminopyridines 0
Pyridines 0
Triazines 0
enasidenib 3T1SS4E7AG
Isocitrate Dehydrogenase EC 1.1.1.41
ivosidenib Q2PCN8MAM6
Glycine TE7660XO1C

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

567-572

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Matteo Dragani (M)

Hematology Department, Gustave Roussy Cancer Centre, Villejuif, France.

Stéphane de Botton (S)

Hematology Department, Gustave Roussy Cancer Centre, Villejuif, France. Electronic address: stephane.debotton@gustaveroussy.fr.

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Classifications MeSH