The role of iron supplementation during epoietin treatment for cancer-related anemia

Med Oncol. 2009;26(1):105-15. doi: 10.1007/s12032-008-9072-0. Epub 2008 May 13.

Abstract

Cancer-related anemia is common and multifactorial in origin. Functional iron deficiency (FID) is now recognized as a cause of iron-restricted erythropoiesis and may be one of the major reasons for lack of response to treatment with Erythropoietic Stimulating Agents (ESAs). Numerous studies have shown that intravenous (IV), but not oral, iron therapy effectively provides sufficient iron for optimal erythropoiesis in anemic patients with chronic renal disease receiving ESA therapy. The use of IV iron has also been suggested in the cancer setting. Six recent studies have tested this assumption and are summarized in this review. Four formulations of IV iron are available in Europe, with different pharmacokinetics, iron bioavailability, and risk of acute adverse drug reactions.

Conclusion: Limited iron stores and FID are common causes of response failure during ESA treatment in cancer patients and should be diagnosed. There is now substantial scientific support for the use of IV iron supplementation to improve response and this has been acknowledged in international and national guidelines. Prospective long-term data on the safety of IV iron in this setting are still awaited. Recommendations concerning the optimal formulation, doses, and schedule of iron supplementation to ESA treatment in cancer-related anemia are provisional awaiting data from prospective, randomized trials.

Publication types

  • Review

MeSH terms

  • Administration, Oral
  • Anemia, Iron-Deficiency* / drug therapy
  • Anemia, Iron-Deficiency* / etiology
  • Drug Administration Schedule
  • Erythropoiesis / drug effects
  • Ferric Compounds / administration & dosage
  • Ferric Compounds / adverse effects
  • Ferric Compounds / pharmacokinetics
  • Ferric Oxide, Saccharated
  • Ferrous Compounds / administration & dosage
  • Ferrous Compounds / adverse effects
  • Ferrous Compounds / pharmacokinetics
  • Glucaric Acid
  • Hematinics / administration & dosage*
  • Hematinics / adverse effects
  • Hematinics / pharmacokinetics
  • Humans
  • Infusions, Intravenous
  • Iron Compounds / administration & dosage*
  • Iron Compounds / adverse effects
  • Iron Compounds / pharmacokinetics
  • Iron, Dietary / administration & dosage
  • Iron, Dietary / adverse effects
  • Iron, Dietary / pharmacokinetics
  • Iron-Dextran Complex / administration & dosage
  • Iron-Dextran Complex / adverse effects
  • Iron-Dextran Complex / pharmacokinetics
  • Maltose / administration & dosage
  • Maltose / adverse effects
  • Maltose / analogs & derivatives
  • Maltose / pharmacokinetics
  • Neoplasms / complications*
  • Randomized Controlled Trials as Topic

Substances

  • Ferric Compounds
  • Ferrous Compounds
  • Hematinics
  • Iron Compounds
  • Iron, Dietary
  • ferric carboxymaltose
  • Maltose
  • Iron-Dextran Complex
  • Ferric Oxide, Saccharated
  • Glucaric Acid
  • ferrous gluconate