Finn William F, Joy Melanie S
Department of Medicine, University of North Carolina, Chapel Hill, NC 27599-7155, USA.
Curr Med Res Opin. 2005 May;21(5):657-64. doi: 10.1185/030079905X41453.
Lanthanum carbonate, a new phosphate binder, is effective in reducing serum phosphorus levels in patients with end-stage renal disease. A 1-year extension study to two randomized controlled studies was conducted to evaluate the long-term safety of lanthanum carbonate in patients who received hemodialysis.
Patients from two previous lanthanum carbonate studies were eligible to continue treatment in a 1-year open-label extension. A total of 77 patients (N = 77; 11 from Study 1, 66 from Study 2) were enrolled in this extension. The mean age of patients was 60.9 years (SD +/- 12.5 years); 65% were male and 35% were female. All patients received lanthanum carbonate at the optimal dose for phosphorus control, determined in their previous study. Safety and tolerability were assessed by monitoring adverse events, laboratory parameters, and vital signs. The number of patients who maintained serum phosphorus levels at < or = 5.9 mg/dL (1.9 mmol/L) was recorded, along with serum calcium, calcium x phosphorus product, and parathyroid hormone levels.
Lanthanum carbonate was well tolerated and was associated with few treatment-related adverse events. The most commonly reported adverse events were nausea (26.0%), peripheral edema (23.4%), and myalgia (20.8%). No treatment-related serious adverse events occurred. By Week 4, the mean serum phosphorus level had decreased by approximately 1 mg/dL to 5.7 +/- 2.0 mg/dL (1.84 +/- 0.7 mmol/L). At the end of the study, the mean pre-dialysis serum phosphorus level was 5.7 +/- 1.4 mg/dL (1.84 +/- 0.5 mmol/L); 53% of patients had controlled phosphorus levels. Calcium x phosphorus product decreased during Week 1 and remained within a clinically acceptable range thereafter. There were no clinically significant changes in serum calcium, or parathyroid hormone levels.
Lanthanum carbonate is well tolerated and is effective for the long-term maintenance of serum phosphorus control in patients with end-stage renal disease.
碳酸镧是一种新型的磷结合剂,可有效降低终末期肾病患者的血清磷水平。对两项随机对照研究进行了为期1年的延长研究,以评估碳酸镧在接受血液透析患者中的长期安全性。
来自之前两项碳酸镧研究的患者有资格在一项为期1年的开放标签延长研究中继续接受治疗。共有77例患者(N = 77;研究1中有11例,研究2中有66例)纳入了该延长研究。患者的平均年龄为60.9岁(标准差±12.5岁);65%为男性,35%为女性。所有患者均接受在其先前研究中确定的控制磷的最佳剂量的碳酸镧。通过监测不良事件、实验室参数和生命体征来评估安全性和耐受性。记录血清磷水平维持在≤5.9mg/dL(1.9mmol/L)的患者数量,以及血清钙、钙磷乘积和甲状旁腺激素水平。
碳酸镧耐受性良好,且与较少的治疗相关不良事件有关。最常报告的不良事件为恶心(26.0%)、外周水肿(23.4%)和肌痛(20.8%)。未发生与治疗相关的严重不良事件。到第4周时,平均血清磷水平已下降约1mg/dL,降至5.