TP53 in AML and MDS: The new (old) kid on the block.
Acute myeloid leukemia
International consensus classification
Myelodysplastic syndrome
TP53
World Health Organization
Journal
Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558
Informations de publication
Date de publication:
07 2023
07 2023
Historique:
received:
25
12
2022
revised:
07
02
2023
accepted:
08
02
2023
medline:
3
7
2023
pubmed:
26
2
2023
entrez:
25
2
2023
Statut:
ppublish
Résumé
MDS and AML are clonal hematopoietic stem cell disorders of increasing incidence, having a variable prognosis based, among others, on co-occurring molecular abnormalities. TP53 mutations are frequently detected in these myeloid neoplasms and portend a poor prognosis with known therapeutic resistance. This article provides a timely review of the complexity of TP53 alterations, providing updates in diagnosis and prognosis based on new 2022 International Consensus Classification (ICC) and World Health Organization (WHO) guidelines. The article addresses optimal testing strategies and reviews current and arising therapeutic approaches. While the treatment landscape for this molecular subgroup is under active development, further exploration is needed to optimize the care of this group of patients with unmet needs.
Identifiants
pubmed: 36841672
pii: S0268-960X(23)00016-4
doi: 10.1016/j.blre.2023.101055
pii:
doi:
Substances chimiques
TP53 protein, human
0
Tumor Suppressor Protein p53
0
Banques de données
ClinicalTrials.gov
['NCT04755244', 'NCT02663518']
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
101055Informations de copyright
Copyright © 2023 Elsevier Ltd. All rights reserved.