Amifostine alone and in combination with erythropoietin for the treatment of favorable myelodysplastic syndrome

Leuk Res. 2001 Feb;25(2):183-5. doi: 10.1016/s0145-2126(00)00108-9.

Abstract

Ten anemic patients with favorable myelodysplastic syndrome (MDS) were first treated with two 5-week courses of amifostine alone (each course consisted of 200 mg/m(2) of the drug given intravenously three times a week for 3 weeks), followed by an additional two courses combined with subcutaneous erythropoietin (EPO) (150 U/kg, three times a week for 8 weeks). The study patients either had previously failed to respond to treatment with EPO or had pretreatment serum EPO levels of more than 100 mU/ml. None of the patients experienced a complete or partial response in anemia or other cytopenias. We conclude that amifostine alone or in combination with EPO has limited therapeutic activity in MDS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Amifostine / administration & dosage
  • Amifostine / therapeutic use*
  • Drug Therapy, Combination
  • Erythropoietin / therapeutic use*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / drug therapy*
  • Recombinant Proteins

Substances

  • Recombinant Proteins
  • Erythropoietin
  • Amifostine