Epoetin alfa 40000 U once weekly and intravenous iron supply in solid tumor patients: early increase of hemoglobin level during chemotherapy

J Exp Clin Cancer Res. 2005 Jun;24(2):197-201.

Abstract

The objective of this observational study was the early evaluation of the impact, a week after the first administration of epoetin alfa 40000 U once weekly and i.v. dose of 62.5 mg sodium ferric gluconate for seven days in improving hemoglobin levels in cancer patients affected by mild/moderate or severe anemia during chemotherapy. Twenty patients affected by solid tumors who received epoetin alfa 40000 U once weekly and daily i.v. sodium ferric gluconate for one week were evaluated: 90% of the patients showed hemoglobin increase, with a median level of hemoglobin increase of 0.73 g/L from baseline, and 50% of them showing a hemoglobin increase > 1 gr/L. The treatment was well tolerated and no adverse event was observed. The early increase of hemoglobin level from baseline is interesting and suggestive for the possibility of achieving an adequate hemoglobin level with a short-term treatment. It is still necessary to further explore the real need of iron supplementation to maintain adequate erythropoiesis prior and during epoetin therapy.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Anemia / drug therapy
  • Anemia / prevention & control
  • Antineoplastic Agents / adverse effects*
  • Antineoplastic Agents / therapeutic use
  • Dietary Supplements
  • Epoetin Alfa
  • Erythropoietin / administration & dosage
  • Erythropoietin / therapeutic use*
  • Female
  • Hematinics / therapeutic use*
  • Hemoglobins / drug effects*
  • Humans
  • Infusions, Intravenous
  • Iron / administration & dosage
  • Iron / metabolism
  • Iron / therapeutic use*
  • Male
  • Middle Aged
  • Neoplasms / blood*
  • Neoplasms / drug therapy*
  • Recombinant Proteins
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Hematinics
  • Hemoglobins
  • Recombinant Proteins
  • Erythropoietin
  • Epoetin Alfa
  • Iron