305 805

Cited 0 times in

한국인 혈액투석 환자의 빈혈 치료에 있어 darbepoetin alfa의 유효성 및 안전성에 대한 제 3상 임상시험

Other Titles
 Randomized, Controlled Trial of Darbepoetin Alfa for the Treatment of Renal Anemia in Hemodialysis Patients 
Authors
 윤수영  ;  최범순  ;  양철우  ;  김용수  ;  방병기  ;  주권욱  ;  김연수  ;  김성권  ;  전진석  ;  김진국  ;  한동철  ;  황승덕  ;  장재원  ;  양원석  ;  박정식  ;  한대석 
Citation
 Korean Journal of Nephrology (대한신장학회지), Vol.24(3) : 429-440, 2005 
Journal Title
Korean Journal of Nephrology(대한신장학회지)
ISSN
 1225-0015 
Issue Date
2005
MeSH
Hemodialysis ; Anemia ; Darbepoetin Alfa ; Recombinant human erythropoietin
Keywords
Hemodialysis ; Anemia ; Darbepoetin Alfa ; Recombinant human erythropoietin
Abstract
Background: Darbepoetin alfa is a new erythropoietic agent with a three fold longer terminal half-life than recombinant human erythropoietin (r-HuEPO). The aim of this randomized, open-label study is to determine whether darbepoetin alfa is as effective as r-HuEPO for the treatment of anemia in hemodialysis patients when administered at a reduced dosing frequency.

Methods: A total 74 Korean hemodialysis patients receiving r-HuEPO therapy by either the intravenous (IV) or subcutaneous (SC) route were randomized to continue r-HuEPO or to receive an equivalent dose of darbepoetin alfa at a reduced dosing frequency. Patients receiving r-HuEPO once weekly changed to once every other week darbepoetin alfa, and those receiving r-HuEPO two or three times weekly chaged to once-weekly darbepoetin alfa. The initial dose of darbepoetin alfa was based on the r-HuEPO dose at the time of entry into the study, using a formula equating the peptide mass of the two molecules (200 IU r-HuEPO=1 ㎍ darbepoetin alfa). The doses of r-HuEPO and darbepoetin alfa were titrated to maintain hemoglobin concentrations within –1.0 to +1.5 g/dL of patients’ baseline values and within a range of 8.0 to 13.0 g/dL for up to 20 weeks (16-week dose-titratio period followed by a 4- week evaluation period). The primary end point was change in hemoglobin level between baseline and the evaluation period.

Results: The mean change in hemoglobin from baseline to the evaluation period was similar in the darbepoetin alfa (–0.03±0.19 g/dL) and r-HuEPO (0.27±0.20 g/dL) groups, and the difference between the two treatments was –0.30 g/dL (95% CI, -0.84 to 0.23). This was not a statistically significant or clinically relevant difference, despite the reduced frequency of darbepoetin alfa administration. The safety profiles of darbepoetin alfa and r-HuEPO were similar.

Conclusion: This study suggests that darbepoetin alfa maintains hemoglobin as effectively as r-HuEPO, but with reduced dose frequency.
Files in This Item:
T200500986.pdf Download
DOI
OAK-2005-05023
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Yoon, Soo Young(윤수영)
Han, Dae Suk(한대석)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/151163
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links