Document Detail


Hydralazine and magnesium valproate as epigenetic treatment for myelodysplastic syndrome. Preliminary results of a phase-II trial.
MedLine Citation:
PMID:  20922525     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Decitabine and azacitidine, two DNA methyltransferase (DNMT) inhibitors, are the current standard of treatment for myelodysplastic syndrome (MDS). Histone deacetylase (HDAC) inhibitors are also being tested against MDS. Both drug classes synergize in their gene reactivating and anticancer activities. The combination of hydralazine and valproate (Transkrip®), a DNMT and HDAC inhibitor, respectively), has been developed as epigenetic therapy under the drug repositioning concept. To evaluate the clinical efficacy and safety of hydralazine and valproate against MDS, an open phase-II study for previously treated patients with MDS was conducted. The hydralazine dose was given according with the acetylator phenotype, and valproate was dosed at 30 mg/kg/day. Response was graded with International Working Group criteria. Toxicity was evaluated by the Common Toxemia Criteria-National Cancer Institute version 3 scale. From November 2007 to January 2010, 12 patients were included. Median age±SD was 53±19.78 years (range, 23-79 years); median time from diagnosis to inclusion in the study was 7.9 months (range 2.6-36.1 months). Median of previous treatment was 2 (range, 1-6). Refractory cytopenia with multilineage dysplasia was diagnosed in ten cases, and refractory anemia with excess of blasts in two. Overall response was documented in six (50%) of 12 cases, including one CR, one PR, and four hematological improvements of the erythroid series. Two patients (16.6%) progressed to acute myeloid leukemia. Hemoglobin increased from 7.4 to 10.3 g/dL (in 13 weeks), neutrophils, from 1.1 to 2.0 (in 3 weeks), and platelets, from 66×10(9) to 72×10(9)/L (in 2 weeks). Transfusional requirements decreased from 2.3 to 0 U bi-monthly for red blood cells and from 0.5 to 0 U bi-monthly for platelets in responding patients. Main toxicities were mild, including somnolence and nausea. Preliminary results of this phase-II study suggest that the combination of hydralazine and valproate is a promising non-toxic and effective therapy for MDS.
Authors:
Myrna Candelaria; Aquileo Herrera; Juan Labardini; Aurora González-Fierro; Catalina Trejo-Becerril; Lucía Taja-Chayeb; Enrique Pérez-Cárdenas; Erick de la Cruz-Hernández; Daymi Arias-Bofill; Silvia Vidal; Eduardo Cervera; Alfonso Dueñas-Gonzalez
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Publication Detail:
Type:  Clinical Trial, Phase II; Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-10-05
Journal Detail:
Title:  Annals of hematology     Volume:  90     ISSN:  1432-0584     ISO Abbreviation:  Ann. Hematol.     Publication Date:  2011 Apr 
Date Detail:
Created Date:  2011-03-10     Completed Date:  2011-05-16     Revised Date:  2013-06-03    
Medline Journal Info:
Nlm Unique ID:  9107334     Medline TA:  Ann Hematol     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  379-87     Citation Subset:  IM    
Affiliation:
Division de Investigación Clínica, Instituto Nacional de Cancerología (INCan), Mexico City, Mexico.
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Azacitidine / analogs & derivatives,  therapeutic use
Cytogenetic Analysis
DNA (Cytosine-5-)-Methyltransferase / antagonists & inhibitors
DNA Modification Methylases / antagonists & inhibitors
Epigenomics*
Female
Histone Deacetylase Inhibitors / blood,  therapeutic use
Humans
Hydralazine / blood,  therapeutic use*
Kaplan-Meier Estimate
Male
Middle Aged
Myelodysplastic Syndromes / blood,  drug therapy*,  genetics*
Treatment Outcome
Valproic Acid / blood,  therapeutic use*
Young Adult
Chemical
Reg. No./Substance:
0/Histone Deacetylase Inhibitors; 320-67-2/Azacitidine; 776B62CQ27/decitabine; 86-54-4/Hydralazine; 99-66-1/Valproic Acid; EC 2.1.1.-/DNA Modification Methylases; EC 2.1.1.37/DNA (Cytosine-5-)-Methyltransferase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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