About: Efficacy and safety of administration of oral iron chelator deferiprone in patients with early myelodysplastic syndrome     Goto   Sponge   NotDistinct   Permalink

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  • Forty-eight patients with early myelodysplastic syndrome (MDS) without excess of blasts, with average initial serum ferritin levels of 2739.5 μg/L (range 825–11287 μg/L), were treated with deferiprone (L1) in a daily dose of 40–90 mg/kg. Median duration of chelation treatment was 10.9 months (range 4–24 months). Chelation was effective (maintained or decreased iron stores) in 16 out of 22 patients (73%) with serum ferritin levels <2000 μg/L in contrast to only 12 out of 26 patients with serum ferritin levels >2000 μg/L. Combination of L1 with recombinant human erythropoietin (rHuEPO) (30–40 kU/week) resulted in effective chelation in five additional patients with serum ferritin levels >3000 μg/L. Incidence of adverse effects was comparable to thatin thalassemic patients. A decreased number of granulocytes was observed in five (13%) patients and agranulocytosis occurred in two patients (4%). Administration of L1 in a daily dose of at least 75 mg/kg may represent an alternative approach
  • Forty-eight patients with early myelodysplastic syndrome (MDS) without excess of blasts, with average initial serum ferritin levels of 2739.5 μg/L (range 825–11287 μg/L), were treated with deferiprone (L1) in a daily dose of 40–90 mg/kg. Median duration of chelation treatment was 10.9 months (range 4–24 months). Chelation was effective (maintained or decreased iron stores) in 16 out of 22 patients (73%) with serum ferritin levels <2000 μg/L in contrast to only 12 out of 26 patients with serum ferritin levels >2000 μg/L. Combination of L1 with recombinant human erythropoietin (rHuEPO) (30–40 kU/week) resulted in effective chelation in five additional patients with serum ferritin levels >3000 μg/L. Incidence of adverse effects was comparable to thatin thalassemic patients. A decreased number of granulocytes was observed in five (13%) patients and agranulocytosis occurred in two patients (4%). Administration of L1 in a daily dose of at least 75 mg/kg may represent an alternative approach (en)
Title
  • Efficacy and safety of administration of oral iron chelator deferiprone in patients with early myelodysplastic syndrome
  • Efficacy and safety of administration of oral iron chelator deferiprone in patients with early myelodysplastic syndrome (en)
skos:prefLabel
  • Efficacy and safety of administration of oral iron chelator deferiprone in patients with early myelodysplastic syndrome
  • Efficacy and safety of administration of oral iron chelator deferiprone in patients with early myelodysplastic syndrome (en)
skos:notation
  • RIV/00023736:_____/11:00009192!RIV12-MZ0-00023736
http://linked.open...avai/riv/aktivita
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  • I, N
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  • 3
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  • 196700
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  • RIV/00023736:_____/11:00009192
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  • deferiprone (L1); myelodysplastic syndrome; iron overload (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
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  • [EAF6F3DD075F]
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  • Hemoglobin
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  • 35
http://linked.open...iv/tvurceVysledku
  • Jonášová, A.
  • Neuwirtová, R.
  • Walterová, L.
  • Čermák, Jaroslav
  • Hochová, I.
  • Vondráková, J.
  • Šišková, M.
http://linked.open...ain/vavai/riv/wos
  • 000290797500005
issn
  • 0363-0269
number of pages
http://bibframe.org/vocab/doi
  • 10.3109/03630269.2011.578515
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