Fang Yu-Wei, Chang Chung-Hsin
Division of Nephrology, Department of Internal Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
Perit Dial Int. 2009 Mar-Apr;29(2):199-203.
Darbepoetin alfa is an erythropoietic-stimulating protein with a threefold longer half-life than recombinant human erythropoietin (rHuEPO) and can be used less frequently in the treatment of renal anemia. The purpose of this single-center single-arm study was to determine whether darbepoetin alfa, when administered at extended dose intervals, is as effective as rHuEPO for the treatment of renal anemia in patients on peritoneal dialysis.
Patients on peritoneal dialysis for at least 3 years receiving stable rHuEPO therapy were shifted to darbepoetin alfa administered every week, or every other week, using the recommended 200:1 conversion factor. The doses of darbepoetin alfa were titrated to maintain hemoglobin within +/-1.0 g/dL of patients' baseline values and within a range of 9.0 - 12.0 g/dL for up to 24 weeks (20-week dose titration period followed by 4-week evaluation period). The primary end point was the change in hemoglobin levels between baseline and evaluation period.
73 patients completed the study; mean age was 52.1 years; 30 males. Mean baseline and evaluation period hemoglobin levels were similar (9.56 +/- 1.11 vs 9.73 +/- 1.41 g/dL, p = 0.248). Mean rHuEPO dose was 92.9 IU/kg/week (equivalent to 0.46 microg/kg/week darbepoetin alfa), which was higher than darbepoetin alfa dose during the evaluation period (0.46 vs 0.34 microg/kg/week, p = 0.038). In addition, ferritin levels decreased (483 +/- 26 vs 396 +/- 19 ng/dL, p = 0.014). The other parameters, such as albumin, C-reactive protein, transferrin saturation, Kt/V, and weekly creatinine clearance showed no statistical difference between the two regimens. No serious or major adverse effects were observed with darbepoetin alfa during the study.
Using lower dosage and frequency, darbepoetin alfa effectively maintains hemoglobin levels in peritoneal dialysis patients previously maintained on erythropoietin beta. Similar effects on hemoglobin can be maintained with even lower levels of ferritin during darbepoetin alfa use. These results show that darbepoetin alfa is safe, effective, and convenient in treating renal anemia in peritoneal dialysis patients.
达比泊汀α是一种促红细胞生成蛋白,其半衰期比重组人促红细胞生成素(rHuEPO)长3倍,可减少治疗肾性贫血时的用药频率。本单中心单臂研究旨在确定延长给药间隔的达比泊汀α在治疗腹膜透析患者肾性贫血方面是否与rHuEPO同样有效。
接受稳定rHuEPO治疗至少3年的腹膜透析患者,按照推荐的200:1换算系数,改为每周或每两周注射一次达比泊汀α。调整达比泊汀α的剂量,使血红蛋白维持在患者基线值±1.0 g/dL范围内,且在9.0 - 12.0 g/dL之间,持续24周(20周剂量调整期,随后是4周评估期)。主要终点是基线期和评估期之间血红蛋白水平的变化。
73例患者完成研究;平均年龄52.1岁;男性30例。基线期和评估期的平均血红蛋白水平相似(9.56±1.11 vs 9.73±1.4 g/dL,p = 0.248)。rHuEPO平均剂量为92.9 IU/kg/周(相当于达比泊汀α 0.46 μg/kg/周),高于评估期达比泊汀α的剂量(0.46 vs 0.34 μg/kg/周,p = 0.038)。此外,铁蛋白水平下降(483±26 vs 396±19 ng/dL,p = 0.014)。其他参数,如白蛋白、C反应蛋白、转铁蛋白饱和度、Kt/V和每周肌酐清除率,在两种治疗方案之间无统计学差异。研究期间使用达比泊汀α未观察到严重或重大不良反应。
使用较低剂量和频率,达比泊汀α能有效维持既往使用促红细胞生成素β治疗的腹膜透析患者的血红蛋白水平。使用达比泊汀α期间,即使铁蛋白水平更低,对血红蛋白的影响仍相似。这些结果表明,达比泊汀α在治疗腹膜透析患者肾性贫血方面安全、有效且方便。