A good response rate to recombinant erythropoietin alone may be expected in selected myelodysplastic patients. A preliminary clinical study

Eur J Haematol. 1996 Jan-Feb;56(1-2):7-11. doi: 10.1111/j.1600-0609.1996.tb00286.x.

Abstract

The use of recombinant erythropoietin for treatment of anemia in myelodysplastic patients has so far produced poorer results than expected. Most clinical studies have been conducted without any selection of patients. In the present study we report our experience with the use of rhEPO in a population of selected MDS subjects. Only patients affected by refractory anemia according to FAB criteria, without significant WBC and platelets reduction, with normal LDH and short history of disease were eligible for the study and were treated with rhEPO at a dosage of 150 mg/kg three times a week for 2 months. Among the 12 so treated patients, 7 (58.3%) achieved complete remission, 2 partial remission and 3 failed to respond. This high response rate makes more than acceptable the cost/benefit ratio for rhEPO in RA patients and may identify a subgroup of patients that can be treated successfully with rhEPO alone.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Anemia / blood
  • Anemia / drug therapy*
  • Erythrocyte Transfusion
  • Erythropoietin / blood
  • Erythropoietin / therapeutic use*
  • Female
  • Ferritins / blood
  • Hematocrit
  • Hemoglobins / metabolism
  • Humans
  • Iron / blood
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / blood
  • Myelodysplastic Syndromes / drug therapy*
  • Myelodysplastic Syndromes / therapy
  • Recombinant Proteins / therapeutic use
  • Treatment Outcome

Substances

  • Hemoglobins
  • Recombinant Proteins
  • Erythropoietin
  • Ferritins
  • Iron