Abstract
Objective:
To evaluate the economic impact of intravenous iron (in the form of intravenous iron preparation of ferric carboxymaltose) in three different clinical settings of iron deficiency anemia: chemotherapy-induced anemia in breast cancer, chemotherapy-induced anemia in digestive cancer, and perioperative anemia in knee and hip surgery.
Methods:
The economic model compared the usual therapeutic strategies of anemia without intravenous iron and strategies including intravenous iron, in each of the three clinical settings selected. Costs related to anemia treatment by erythropoiesis-stimulating agents (ESA), blood transfusion, and intravenous iron were estimated and compared inside each setting. Cost savings were calculated from the French healthcare payer perspective. Data included in the economic model were obtained from scientific literature, public health agencies, and medical experts.
Results:
The most prominent annual cost savings were observed in chemotherapy-induced anemia in breast cancer (€997 and €360 per patient for metastatic and non-metastatic breast cancers, respectively; global cost saving, €33.6 million). This large impact of intravenous iron on costs was mainly explained by both a lower number of women treated and lower ESA dosing. Mean annual cost saving in digestive cancers and knee and hip surgery were estimated to €168 and €216 per patient and global cost savings of €7.5 and €12.1 million, respectively. Overall, annual cost savings in these three settings were estimated to €53 million including €39 million for ESA cost savings. Sensitivity analysis showed that strategies including intravenous iron remained cost-effective even with wide variations in the assumptions, particularly for cost savings on ESA.
Limitations:
Economic model based on literature data and expert opinions.
Conclusions:
The present economic model suggests that use of intravenous iron, according to recommendations of international guidelines, is cost saving, particularly in chemotherapy-induced anemia in breast cancers.
Transparency
Declaration of funding
The study was sponsored by Vifor Pharma.
Declaration of financial/other relationships
LM and JW are employees of Vifor Pharma; the other authors have no financial interests to disclose directly or indirectly related to the research in the manuscript.
Acknowledgments
This study was presented in part at the ISPOR 16th Annual International Meeting, May 21–25, 2011, Baltimore, MD, USA. The authors would like to thank for their help Jacques N. Biot, Peter Branhaufer, Lorraine Zakin and Francis Beauvais.
Notes
*Ferinject is a registered trade name of Vifor Pharma AG, Switzerland.