Predictive Model for Infection Risk in Myelodysplastic Syndromes, Acute Myeloid Leukemia, and Chronic Myelomonocytic Leukemia Patients Treated With Azacitidine; Azacitidine Infection Risk Model: The Polish Adult Leukemia Group Study.
Adult
Aged
Aged, 80 and over
Anti-Bacterial Agents
/ therapeutic use
Antibiotic Prophylaxis
/ methods
Antifungal Agents
/ therapeutic use
Antimetabolites, Antineoplastic
/ adverse effects
Azacitidine
/ adverse effects
Bacterial Infections
/ chemically induced
Female
Health Status Indicators
Humans
Kaplan-Meier Estimate
Leukemia, Myeloid, Acute
/ drug therapy
Leukemia, Myelomonocytic, Chronic
/ drug therapy
Male
Middle Aged
Mycoses
/ chemically induced
Myelodysplastic Syndromes
/ drug therapy
Poland
/ epidemiology
Proportional Hazards Models
Retrospective Studies
Risk Assessment
/ methods
Treatment Outcome
Acute leukemia
Azacitidine
Chronic myelomonocytic leukemia
Infections
Myelodysplastic syndromes
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:
05 2019
05 2019
Historique:
received:
22
10
2018
revised:
04
01
2019
accepted:
10
01
2019
pubmed:
23
3
2019
medline:
7
7
2020
entrez:
23
3
2019
Statut:
ppublish
Résumé
Myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), and acute myeloid leukemia (AML) patients, including those treated with azacitidine, are at increased risk for serious infections. The aim of our study was to identify patients with higher infectious risk at the beginning of azacitidine treatment. We performed a retrospective evaluation of 298 MDS/CMML/AML patients and included in the analysis 232 patients who completed the first 3 cycles of azacitidine therapy or developed Grade III/IV infection before completing the third cycle. Overall, 143 patients (62%) experienced serious infection, and in 94 patients (41%) infection occurred within the first 3 cycles. The following variables were found to have the most significant effect on the infectious risk in multivariate analysis: red blood cell transfusion dependency (odds ratio [OR], 2.38; 97.5% confidence interval [CI], 1.21-4.79), neutropenia <0.8 × 10 We selected a subset with high early risk for serious infection and worse clinical outcome among patients treated with azacitidine.
Sections du résumé
BACKGROUND
Myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), and acute myeloid leukemia (AML) patients, including those treated with azacitidine, are at increased risk for serious infections. The aim of our study was to identify patients with higher infectious risk at the beginning of azacitidine treatment.
PATIENTS AND METHODS
We performed a retrospective evaluation of 298 MDS/CMML/AML patients and included in the analysis 232 patients who completed the first 3 cycles of azacitidine therapy or developed Grade III/IV infection before completing the third cycle.
RESULTS
Overall, 143 patients (62%) experienced serious infection, and in 94 patients (41%) infection occurred within the first 3 cycles. The following variables were found to have the most significant effect on the infectious risk in multivariate analysis: red blood cell transfusion dependency (odds ratio [OR], 2.38; 97.5% confidence interval [CI], 1.21-4.79), neutropenia <0.8 × 10
CONCLUSION
We selected a subset with high early risk for serious infection and worse clinical outcome among patients treated with azacitidine.
Identifiants
pubmed: 30898482
pii: S2152-2650(18)31510-6
doi: 10.1016/j.clml.2019.01.002
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
Antifungal Agents
0
Antimetabolites, Antineoplastic
0
Azacitidine
M801H13NRU
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
264-274.e4Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.