Treatment of chemotherapy-induced anemia with recombinant human erythropoietin in cancer patients

J Clin Oncol. 1991 Nov;9(11):2021-6. doi: 10.1200/JCO.1991.9.11.2021.

Abstract

Thirty patients with chemotherapy-induced anemia were treated with recombinant human erythropoietin for 4 weeks. In this dose-escalation study, cohorts of five to eight patients were treated per dose level. The doses of erythropoietin were 25, 50, 100, 200, or 300 IU/kg/d given intravenously for 5 days each week. Of 30 patients, 15 (50%) had a greater than 10% increase of their hemoglobin (Hb) values and were considered responders. At the two highest dose levels, 11 of 13 patients (85%) responded. In the 15 responding patients, the mean Hb level increased by 1.7 g/dL from baseline compared with an average decrease of 1.5 g/dL in the previous cycles of chemotherapy without erythropoietin administration. Recombinant human erythropoietin is effective in ameliorating chemotherapy-induced anemia when administered in adequate doses.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Anemia / chemically induced
  • Anemia / drug therapy*
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects*
  • Cohort Studies
  • Dose-Response Relationship, Drug
  • Drug Evaluation
  • Erythropoietin / pharmacology
  • Erythropoietin / therapeutic use*
  • Female
  • Hemoglobins / drug effects*
  • Humans
  • Injections, Intravenous
  • Logistic Models
  • Male
  • Middle Aged
  • Recombinant Proteins / pharmacology
  • Recombinant Proteins / therapeutic use

Substances

  • Hemoglobins
  • Recombinant Proteins
  • Erythropoietin