Department of Pharmacy, North General Hospital, New York, New York 10035, USA.
Pharmacotherapy. 2010 Jan;30(1):70-9. doi: 10.1592/phco.30.1.70.
Ferumoxytol is an intravenous iron preparation for treatment of the anemia of chronic kidney disease (CKD). It is a carbohydrate-coated, superparamagnetic iron oxide nanoparticle. Because little free iron is present in the preparation, doses of 510 mg have been administered safely in as little as 17 seconds. Two prospective, randomized studies compared two doses of ferumoxytol 510 mg given in 5 +/- 3 days with 3 weeks of oral iron 200 mg/day (as ferrous fumarate) in anemic patients with CKD. One study enrolled 304 patients with stages 1-5 CKD (predialysis), and the other study enrolled 230 patients with stage 5D CKD (undergoing hemodialysis). In both studies, a greater increase in hemoglobin level from baseline to end of study (day 35) was noted in patients who received ferumoxytol compared with those who received oral iron (mean +/- SD 0.82 +/- 1.24 vs 0.16 +/- 1.02 g/dl in patients with stages 1-5 CKD and 1.02 +/- 1.13 vs 0.46 +/- 1.06 g/dl in patients with stage 5D CKD, p<0.001). A greater proportion of both predialysis and hemodialysis patients who received ferumoxytol had hemoglobin level increases from baseline of 1 g/dl or more compared with those who received oral iron (p<0.001). In a prospective, double-blind, crossover study of more than 700 patients with CKD stages 1-5D that compared the safety of ferumoxytol with normal saline injection, the rates of treatment-related adverse events were 5.2% and 4.5%, respectively. Serious treatment-related adverse events were seen in one patient in each treatment group. The most common adverse events with ferumoxytol occurred at the injection site (bruising, pain, swelling, erythema). Dizziness, nausea, pruritus, headache, and fatigue occurred in less than 2% of patients receiving ferumoxytol, with a similar frequency noted after administration of normal saline. In short-term studies, intravenous ferumoxytol was safely and rapidly administered, and was more effective than oral iron therapy in increasing hemoglobin levels in anemic patients with CKD. Long-term clinical trials with clinical outcomes and studies comparing ferumoxytol with other parenteral iron agents will help define the role of ferumoxytol in treating the anemia of CKD.
铁氧体是一种用于治疗慢性肾脏病(CKD)贫血的静脉铁制剂。它是一种碳水化合物包裹的超顺磁性氧化铁纳米颗粒。由于制剂中几乎不存在游离铁,因此在短短 17 秒内已安全给予 510 毫克的剂量。两项前瞻性、随机研究比较了铁氧体 510 毫克两种剂量,在 5 +/- 3 天内给予与 3 周内口服铁 200 毫克/天(富马酸亚铁)在患有 CKD 的贫血患者中的疗效。一项研究纳入了 304 名 CKD 1-5 期(透析前)患者,另一项研究纳入了 230 名 CKD 5D 期(血液透析)患者。在这两项研究中,与接受口服铁治疗的患者相比,接受铁氧体治疗的患者血红蛋白水平从基线到研究结束(第 35 天)的升高更为明显(CKD 1-5 期患者的平均 +/- SD 为 0.82 +/- 1.24 与 0.16 +/- 1.02 g/dl,CKD 5D 期患者为 1.02 +/- 1.13 与 0.46 +/- 1.06 g/dl,p<0.001)。与接受口服铁治疗的患者相比,接受铁氧体治疗的透析前和透析患者中有更大比例的患者血红蛋白水平升高 1 g/dl 或更高(p<0.001)。在一项超过 700 名 CKD 1-5D 期患者的前瞻性、双盲、交叉研究中,比较了铁氧体与生理盐水注射的安全性,治疗相关不良事件的发生率分别为 5.2%和 4.5%。在每个治疗组中,各有 1 名患者发生严重的治疗相关不良事件。铁氧体最常见的不良反应发生在注射部位(瘀伤、疼痛、肿胀、红斑)。头晕、恶心、瘙痒、头痛和疲劳在接受铁氧体治疗的患者中发生率低于 2%,在给予生理盐水后也有类似的频率。在短期研究中,静脉铁氧体安全且快速给药,在增加 CKD 贫血患者的血红蛋白水平方面比口服铁治疗更有效。具有临床结局的长期临床试验和比较铁氧体与其他肠外铁剂的研究将有助于确定铁氧体在治疗 CKD 贫血中的作用。