Randomized trial of darbepoetin alfa for treatment of renal anemia at a reduced dose frequency compared with rHuEPO in dialysis patients

被引:148
作者
Vanrenterghem, Y
Bárány, P
Mann, JFE
Kerr, PG
Wilson, J
Baker, NF
Gray, SJ
机构
[1] Univ Hosp Leuven, Dept Nephrol, B-3000 Louvain, Belgium
[2] Huddinge Univ Hosp, Div Renal Med, Stockholm, Sweden
[3] LMU, Schwabing Gen Hosp, Munich, Germany
[4] Monash Med Ctr, Dept Nephrol, Melbourne, Vic, Australia
[5] Amgen Ltd, Cambridge, England
关键词
darbepoetin alfa; novel erythropoiesis stimulating protein (NESP); chronic renal failure; hemodialysis; peritoneal dialysis; anemia; recombinant human erythropoietin;
D O I
10.1046/j.1523-1755.2002.00657.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Darbepoetin alfa is a glycoprotein with a threefold longer terminal half-life than recombinant human erythropoietin (rHuEPO). We aimed to determine whether darbepoetin alfa is as effective and well tolerated as rHuEPO for treating renal anemia in dialysis patients when administered at a reduced dose frequency. Methods. A total of 522 European and Australian hemodialysis and peritoneal dialysis patients receiving stable rHuEPO therapy by either the intravenous (IV) or subcutaneous (SC) route were randomized, open-label in a 1:2 ratio to continue rHuEPO or to receive an equivalent dose of darbepoetin alfa at a reduced dose frequency. Patients receiving rHuEPO once weekly changed to once every other week darbepoetin alfa, and those receiving rHuEPO two or three times weekly changed to once-weekly darbepoetin alfa. The doses of rHuEPO and darbepoetin alfa were titrated to maintain hemoglobin close to the patient's baseline level for up to 52 weeks. The primary endpoint was the change in hemoglobin between baseline and the evaluation period at weeks 25 to 32 of treatment. Results. The mean change in hemoglobin from baseline to the evaluation period was similar in the darbepoetin alfa (-0.03 g/dL; SE 0.11) and rHuEPO (-0.06 g/dL; SE 0.13) groups, and the difference between the two treatments was 0.03 g/dL (95% CI -0.16, 0.21.). This was not a statistically significant or clinically relevant difference, despite the reduced frequency of darbepoetin alfa administration. At the end of the evaluation period, greater than or equal to95% of patients had their hemoglobin successfully maintained on their assigned dose frequency for darbepoetin alfa (once weekly and once every other week) and rHuEPO (once, twice and three times weekly). The safety profiles of darbepoetin alfa and rHuEPO were similar, and no antibodies to either treatment were detected. Conclusions. Darbepoetin alfa maintains hemoglobin as effectively as rHuEPO, but with a reduced dose frequency.
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收藏
页码:2167 / 2175
页数:9
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