Prognostic value of TP53 gene mutations in myelodysplastic syndromes and acute myeloid leukemia treated with azacitidine
Abstract
TP53 mutations are found in 5-10% of MDS and AML, where they are generally associated with complex karyotype and an overall poor prognosis. However, the impact of TP53 mutations in MDS treated with azacitidine (AZA) remains unclear. We analyzed TP53 mutations in 62 patients with high risk MDS or AML treated with AZA. A TP53 mutation was found in 23 patients (37.1%), associated with complex karyotype in 18 (78.3%) of them. TP53 mutations had no significant impact on response or complete response to AZA (p=0.60 and p=0.26, respectively). By univariate analysis, OS was negatively influenced by the presence of TP53 mutation (median OS 12.4 months versus 23.7 months, p<10(-4)), abnormal cytogenetics (median OS 14.4 months vs 33 months, p=0.02) complex cytogenetics (median OS 12.7 months versus 23.7 months, p=0.0005), and a diagnosis of AML (median 14.5 months vs 21.2 months for MDS or CMML, p=0.02). By multivariate analysis, only TP53 mutational status (HR 2.89 (95% confidence interval 1.38-6.04; p=0.005) retained statistical significance for OS. Results were similar when the analysis was restricted to MDS and CMML patients, excluding AML (HR=2.46 (95% confidence interval: 1.1-6.4); p=0.04)). Thus, TP53 mutations strongly correlated with poorer survival in higher risk MDS and AML treated with AZA.
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Remissions in TP53-mutant patients are brief, with a median overall survival ranging from 5 to 12 months.
“However, remissions in TP53-mutant patients are brief with a median overall survival (OS) ranging from 5 to 12 months,8,9,12,13,15-17”
From Eprenetapopt (APR-246) and Azacitidine in <i>TP53</i> -Mutant Myelodysplastic Syndromes (2021) · cites this paper as [15]
In mTP53 mutant MDS with HMA, the CR rate is ~20% with a median OS of less than 12 months.
“In mTP53 mutant MDS with HMA, the CR rate is ~20% with a median OS of less than 12 months.”
From Long‐term follow‐up and combined Phase 2 results of eprenetapopt and azacitidine in patients with <i>TP53</i> mutant MDS/AML (2025) · cites this paper as [16]
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- Authors
- Bally, C., Adès, L., Renneville, A., Sebert, M., Eclache, V., Preudhomme, C., Mozziconacci, M.-J., de The, H., Lehmann-Che, J., & Fenaux, P.
- Affiliations
- Assistance Publique – Hôpitaux de Paris (FR)
- Centre Hospitalier Universitaire de Lille (FR)
- Corresponding author
- Fenaux, Pierre
- Venue
- Leukemia Research
- Publisher
- Elsevier BV
- Published
- 2014-07
- Volume
- 38
- Issue
- 7
- Pages
- 751-755
- ISSN
- 0145-2126 (ISSN-L)
- OpenAlex
- W2062135903
- Cited by
- 162
- References
- 30
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 9 · 2023: 16 · 2022: 7 · 2021: 16 · 2020: 18 · 2019: 9 · 2018: 15 · 2017: 19 · 2016: 13 · 2015: 21 · 2014: 5
- FWCI
- 13.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Leukemia Research (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinoids in leukemia and cellular processes
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Keywords
- TP53 mutation, myelodysplastic syndrome, acute myeloid leukemia, azacitidine, prognostic factors, overall survival, complex karyotype, cytogenetics, high-risk MDS, chronic myelomonocytic leukemia, treatment response
- MeSH terms
- Adult, Aged, Aged, 80 and over, Antimetabolites, Antineoplastic, Azacitidine, Female, Humans, Male, Middle Aged, Mutation, Myelodysplastic Syndromes, Prognosis, Leukemia, Myeloid, Acute, Genes, p53
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