Identification of predictive factors for overall survival at baseline and during azacitidine treatment in high-risk myelodysplastic syndrome patients treated in the clinical practice.
Adult
Aged
Aged, 80 and over
Antimetabolites, Antineoplastic
/ therapeutic use
Azacitidine
/ therapeutic use
Drug Administration Schedule
Female
Humans
Male
Middle Aged
Myelodysplastic Syndromes
/ drug therapy
Opportunistic Infections
/ drug therapy
Prognosis
Retrospective Studies
Risk Factors
Survival Analysis
Treatment Outcome
Azacitidine
Hypomethylating agent
Myelodysplastic syndromes
Real-life
Journal
Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
03
03
2019
accepted:
28
05
2019
pubmed:
7
6
2019
medline:
26
7
2019
entrez:
7
6
2019
Statut:
ppublish
Résumé
The outcome of high-risk myelodysplastic syndrome (MDS) patients treated with 5-azacitidine (5-AZA) in the real-life setting remains largely unknown. We evaluated 110 MDS patients (IPSS intermediate 2/high) treated outside of clinical trials at a single institution between September 2003 and January 2017. Median duration of therapy was 9.5 cycles. The overall survival (OS) of the whole cohort was 66.1% at 1 year and 38.3% at 2 years. No differences in terms of OS were observed with regard to gender (p = 0.622) and age at baseline (< 65 years, 65-75, and > 75 years, p = 0.075). According to the IPSS-R, the very high-risk group had an inferior 2-year OS (17%) compared with intermediate-group patients (64%, p < 0.001). Transfusion independency at baseline was identified as a favorable prognostic factor on 1-year (66.8%) and 2-year OS (43.4%) (p < 0.001). After four cycles, the persistence of bone marrow blasts > 10% identified patients with a worse outcome, with a 2-year OS of 9.4% (p = 0.002). The occurrence of an infection during the first four cycles impacted on the 2-year OS (31.6% vs 58.3% in patients without infections, p = 0.032). Patients receiving at least 24 cycles of the drug have a 5-year OS of 38.2%. This analysis allowed to identify features at baseline or during treatment with 5-AZA associated with a different 2-year OS.
Identifiants
pubmed: 31168652
doi: 10.1007/s00277-019-03724-9
pii: 10.1007/s00277-019-03724-9
doi:
Substances chimiques
Antimetabolites, Antineoplastic
0
Azacitidine
M801H13NRU
Types de publication
Journal Article
Langues
eng