Abstract
Background:
The prognosis of myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML) is very heterogeneous.
Patients and methods:
We analyzed the prognostic value of several genes in a cohort of 85 MDS and AML patients.
Results:
Overexpression of glycogen synthase 1 and macrophage migration inhibitory factor genes had an adverse outcome in multivariate analysis (P = .003 and P < .001, respectively). Furthermore, the higher expression of myelocytomatosis oncogene was associated with a lower response to azacitidine (P = .03).
Conclusion:
In the current study we identified a specific gene expression profile as prognostic factors for response to azacitidine and survival in MDS and AML.
Keywords:
Acute leukemia; Azacitidine; Gene expression; Myelodysplastic syndromes; Prognosis.
Copyright © 2015 Elsevier Inc. All rights reserved.
MeSH terms
-
Aged
-
Aged, 80 and over
-
Antimetabolites, Antineoplastic / therapeutic use
-
Azacitidine / therapeutic use
-
Gene Expression Profiling
-
Gene Expression*
-
Genes, myc*
-
Glycogen Synthase / genetics*
-
Humans
-
Hypoxia / genetics
-
Intramolecular Oxidoreductases / genetics*
-
Leukemia, Myeloid, Acute / diagnosis
-
Leukemia, Myeloid, Acute / drug therapy*
-
Leukemia, Myeloid, Acute / genetics*
-
Leukemia, Myeloid, Acute / mortality
-
Macrophage Migration-Inhibitory Factors / genetics*
-
Middle Aged
-
Myelodysplastic Syndromes / diagnosis
-
Myelodysplastic Syndromes / drug therapy*
-
Myelodysplastic Syndromes / genetics*
-
Myelodysplastic Syndromes / mortality
-
Prognosis
-
Survival Analysis
-
Treatment Outcome
Substances
-
Antimetabolites, Antineoplastic
-
Macrophage Migration-Inhibitory Factors
-
Glycogen Synthase
-
Intramolecular Oxidoreductases
-
MIF protein, human
-
Azacitidine