Abstract
The prognosis of acute myeloid leukemia (AML) in elderly (≥65 years) patients is poor and treatment remains non-consensual especially for those who are not eligible for intensive therapies. Our group has shown that in vitro the iron chelator deferasirox (DFX) synergizes with vitamin D (VD) to promote monocyte differentiation in primary AML cells. Herein, we present results from a retrospective case-control study in which the association of DFX (1-2 g/d) and 25-hydroxycholecalciferol (100,000 IU/week) (DFX/VD) was proposed to patients following demethylating agents failure. Median survival of patients treated with DFX/VD combination (n = 17) was significantly increased in comparison with matched patients receiving best supportive care (BSC) alone (n = 13) (10.4 versus 4 months respectively). In addition, the only factor associated to an increased overall survival in DFX/VD-treated patients was serum VD levels. We conclude that DFX/VD treatment correlated with increased overall survival of AML patients in this retrospective cohort of elderly patients.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aged
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Aged, 80 and over
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Antineoplastic Combined Chemotherapy Protocols / pharmacology
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Azacitidine / pharmacology*
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Azacitidine / therapeutic use
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Benzoates / administration & dosage
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Case-Control Studies
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Cell Differentiation / drug effects
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DNA (Cytosine-5-)-Methyltransferases / antagonists & inhibitors
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Deferasirox
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Drug Resistance, Neoplasm
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Drug Synergism
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Female
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Humans
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Kaplan-Meier Estimate
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Leukemia, Myeloid, Acute / drug therapy*
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Leukemia, Myeloid, Acute / mortality
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Leukemia, Myeloid, Acute / pathology
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Male
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Middle Aged
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Myeloid Cells / drug effects
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Myeloid Cells / physiology
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Proportional Hazards Models
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Retrospective Studies
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Treatment Outcome
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Triazoles / administration & dosage
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Vitamin D / administration & dosage
Substances
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Benzoates
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Triazoles
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Vitamin D
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DNA (Cytosine-5-)-Methyltransferases
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Azacitidine
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Deferasirox
Grants and funding
The Fondation pour la Recherche Médicale (FRM), the fondation de France, Ligue contre le cancer, le cancéropole, Institut National du Cancer (INCA), association Laurette Fugain and the Association pour la Recherche contre le Cancer (ARC) supported this work. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.