NDT Advance Access originally published online on September 22, 2007
Nephrology Dialysis Transplantation 2008 23(1):301-308; doi:10.1093/ndt/gfm579
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Darbepoetin alpha in lower-than-equimolar doses maintains haemoglobin levels in stable haemodialysis patients converting from epoetin alpha/beta
1Division of Nephrology, Kantonsspital Aarau, 2Regionalspital Emmental, Burgdorf, 3Hôpital regional, Porrentruy, 4Waid Spital, Zürich, 5PFC Pharma Focus Ltd, Volketswil and 6Clinique Cécil, Lausanne
Correspondence to: H. Andreas Bock, Division of Nephrology, Kantonsspital, Buchserstrasse, CH-5001 Aarau, Switzerland. Email: andreas.bock{at}ksa.ch
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Abstract |
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Background. The conversion of patients on stable epoetin therapy to darbepoetin alpha is usually carried out according to the ‘1 µg darbepoetin = 200 U epoetin’ rule, which is based on the protein content of the two compounds. Since several observations have suggested that this conversion factor leads to an overestimate of the required darbepoetin dose, the present multicentre study was designed to assess the true conversion ratio by prospectively evaluating the change in darbepoetin alpha dose after conversion from epoetin, which was required to keep haemoglobin (Hb) stable.
Methods. Haemodialysis patients with stable Hb and maintained on either s.c. or i.v. epoetin (alpha or beta) were switched to intravenously administered darbepoetin alpha according to the 1:200 rule. Subjects treated with epoetin two or three times per week received one weekly dose of darbepoetin alpha, subjects on weekly epoetin received darbepoetin alpha every 2 weeks. For 20 weeks, darbepoetin alpha was changed every 2 weeks according to a pre-specified algorithm, if this was needed to keep Hb within ±1.0 g/dl of each subject's individual baseline. Thereafter, patients entered a 4-week evaluation period.
Results. One hundred ad thirty-two patients in 17 Swiss centres were enrolled and 100 completed the study throughout the evaluation period. While mean Hb was maintained stable between baseline and evaluation period (11.8 ± 0.6 g/dl in both), the mean required darbepoetin alpha dose decreased from 34.7 ± 2.1 to 26.0 ± 1.8 µg (–25%, P < 0.0001), yielding a mean final conversion ratio of 1:336. A dose decrease was observed in 56 patients, no dose change in 28 and an increase in 16 patients. Dose reduction strongly depended on baseline epoetin dose: no dose reduction was required for baseline epoetin doses <5000 U/week, whereas a 37% lower mean dose was necessary for baseline doses of 7000–10 000 U/week. The darbepoetin alpha dose reduction did not depend on the previous epoetin type (alpha or beta) or the previous epoetin administration route (i.v. vs s.c.).
Conclusions. The mean darbepoetin alpha dose needed to keep Hb stable in patients previously treated with epoetin is significantly lower than the equimolar dose. Although the equimolar 1:200 conversion ratio is appropriate for lower epoetin doses (<5000 IU/week), the darbepoetin dose for patients converting from 
5000 IU of epoetin per week is more likely to follow a 1:250 to 1:350 conversion rule. If pricing is based on the 1:200 rule such as in Switzerland, this may translate into cost savings.
Keywords: anaemia; darbepoetin; end-stage renal disease; epoetin; haemoglobin
*The investigators are listed in the Appendix.
Received for publication: 13.12.06
Accepted in revised form: 30. 7.07
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