Jadoul Michel, Vanrenterghem Yves, Foret Michel, Walker Rowan, Gray Stephen J
Department of Nephrology, Cliniques Saint Luc, Université Catholique de Louvain, Brussels, Belgium.
Nephrol Dial Transplant. 2004 Apr;19(4):898-903. doi: 10.1093/ndt/gfh021.
Darbepoetin alfa, a glycoprotein that stimulates erythropoiesis by the same mechanism as endogenous erythropoietin, has a 3-fold longer terminal half-life than recombinant human erythropoietin, allowing for an extended dosing interval. Darbepoetin alfa is currently recommended for once-weekly and once every 2 weeks administration in patients with chronic renal failure (CRF). The objective of this study was to explore once-monthly administration in this patient population.
Clinically stable dialysis patients (mean haemoglobin concentration, 10.0-13.0 g/dl) receiving stable darbepoetin alfa therapy administered once every 2 weeks in a long-term treatment study were converted to darbepoetin alfa once every 3 weeks for 20 weeks and then, if haemoglobin concentrations were successfully maintained between 10.0 and 13.0 g/dl, were converted to darbepoetin alfa once every 4 weeks for 20 weeks. The darbepoetin alfa dose was titrated to maintain haemoglobin within a target range (-1.0 to +1.5 g/dl of baseline haemoglobin, and between 10.0 and 13.0 g/dl). Success with the extended dosing interval was defined as maintenance of mean haemoglobin >/=10.0 g/dl during a 4-week evaluation at the end of the dosing period.
Of the 54 patients who entered the study, 38 patients were converted to darbepoetin alfa administered once every 4 weeks. Of these, 36 patients were considered evaluable and 30 (83%) of those evaluable patients successfully maintained the target haemoglobin. For successful patients the mean (SD) haemoglobin during evaluation was 11.16 (0.60) g/dl, and the mean change in haemoglobin from baseline to evaluation was -0.26 g/dl (95% CI: -0.51, -0.01). The median change from baseline in average weekly darbepoetin alfa dose was 1.61 microg (95% CI: 0.00, 4.75). Adverse events were consistent with those expected for this patient population.
Darbepoetin alfa, administered once monthly, maintained haemoglobin effectively and safely in most dialysis patients stabilized previously on once every 2 weeks dosing. Once-monthly dosing may optimize anaemia management for patients with CRF and for health care providers.
达比加群酯是一种糖蛋白,通过与内源性促红细胞生成素相同的机制刺激红细胞生成,其终末半衰期比重组人促红细胞生成素长3倍,从而允许延长给药间隔。目前推荐对慢性肾衰竭(CRF)患者每周给药一次或每2周给药一次达比加群酯。本研究的目的是探讨在该患者群体中每月给药一次的情况。
在一项长期治疗研究中,接受每2周一次稳定剂量达比加群酯治疗且临床稳定的透析患者(平均血红蛋白浓度为10.0 - 13.0 g/dl),先转换为每3周一次达比加群酯治疗20周,然后,如果血红蛋白浓度成功维持在10.0至13.0 g/dl之间,则转换为每4周一次达比加群酯治疗20周。达比加群酯剂量进行滴定以将血红蛋白维持在目标范围内(基线血红蛋白值±1.0至±1.5 g/dl,且在10.0至13.0 g/dl之间)。延长给药间隔的成功定义为在给药期结束时的4周评估期间平均血红蛋白维持≥10.0 g/dl。
进入研究的54例患者中,38例患者转换为每4周一次达比加群酯给药。其中,36例患者被认为可评估,这些可评估患者中有30例(83%)成功维持了目标血红蛋白水平。对于成功的患者,评估期间的平均(标准差)血红蛋白为11.16(0.60)g/dl,从基线到评估时血红蛋白的平均变化为 - 0.26 g/dl(95%可信区间: - 0.51, - 0.01)。达比加群酯平均每周剂量从基线的中位数变化为1.61μg(95%可信区间:0.00,4.75)。不良事件与该患者群体预期的一致。
对于先前每2周给药一次已稳定的大多数透析患者,每月给药一次达比加群酯可有效且安全地维持血红蛋白水平。每月给药一次可能会优化CRF患者及医疗服务提供者的贫血管理。