Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/22977
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dc.contributor.authorBourantas, K. L.en
dc.contributor.authorTsiara, S.en
dc.contributor.authorChristou, L.en
dc.contributor.authorRepousis, P.en
dc.contributor.authorKonstantinidou, P.en
dc.contributor.authorBai, M.en
dc.contributor.authorSeferiadis, K.en
dc.date.accessioned2015-11-24T19:29:32Z-
dc.date.available2015-11-24T19:29:32Z-
dc.identifier.issn0001-5792-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/22977-
dc.rightsDefault Licence-
dc.subjectAgeden
dc.subjectBone Marrow/pathologyen
dc.subjectErythropoietin/*therapeutic useen
dc.subjectFemaleen
dc.subjectGranulocyte-Macrophage Colony-Stimulating Factor/*therapeutic useen
dc.subjectHemoglobins/metabolismen
dc.subjectHumansen
dc.subjectInterferon-alpha/*therapeutic useen
dc.subjectLeukocyte Counten
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectPlatelet Counten
dc.subjectPrimary Myelofibrosis/blood/pathology/*therapyen
dc.subjectRecombinant Proteins/therapeutic useen
dc.subjectSpleen/pathologyen
dc.subjectbeta 2-Microglobulin/metabolismen
dc.titleCombination therapy with recombinant human erythropoietin, interferon-alpha-2b and granulocyte-macrophage colony-stimulating factor in idiopathic myelofibrosisen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/8701705-
heal.identifier.secondaryhttp://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000203720-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1996-
heal.abstractSeven patients, 3 men and 4 women 48-72 years of age and suffering from idiopathic myelofibrosis were given a combination of recombinant human erythropoietin (r-hu-Epo), interferon-alpha-2b (IFN) and GM-CSF, in an attempt to treat their pancytopenia and marrow fibrosis. The dose of r-hu-Epo was 200 U/kg 3 times weekly, that of IFN was 3 x 10(6)/U 3 times weekly, and that of GM-CSF was 250 micrograms/m2/daily. The duration of therapy ranged from 3 to 6 months for r-hu-Epo and IFN and was 3 weeks for GM-CSF. The treatment regimen had a beneficial effect on all patients. The levels of hemoglobin increased in all patients but particularly in 5 (2 of whom had been dependent on red blood cell transfusions). Splenomegaly decreased significantly in 4 patients. Fibrosis in the bone marrow decreased in 2 patients. Three patients also had an increase in the number of white blood cells during the therapy with GM-CSF. We observed mild side effects in 6 of our patients. One patient had severe side effects from IFN and treatment was discontinued. In conclusion, the combination of r-hu-Epo, IFN and GM-CSF may improve the anemia (due to r-hu-Epo), increase the white blood cell count (due to GM-CSF) and reduce the marrow fibrosis (probably due to IFN) in patients with idiopathic myelofibrosis.en
heal.journalNameActa Haematolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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