Lindberg Jill S, Culleton Bruce, Wong Gordon, Borah Michael F, Clark Roderick V, Shapiro Warren B, Roger Simon D, Husserl Fred E, Klassen Preston S, Guo Matthew D, Albizem Moetaz B, Coburn Jack W
New Orleans Nephrology Associates, 4228 Houma Boulevard, Metairie, LA 70006, USA.
J Am Soc Nephrol. 2005 Mar;16(3):800-7. doi: 10.1681/ASN.2004060512. Epub 2005 Feb 2.
Management of secondary hyperparathyroidism is challenging with traditional therapy. The calcimimetic cinacalcet HCl acts on the calcium-sensing receptor to increase its sensitivity to calcium, thereby reducing parathyroid hormone (PTH) secretion. This phase 3, multicenter, randomized, placebo-controlled, double-blind study evaluated the efficacy and safety of cinacalcet in hemodialysis (HD) and peritoneal dialysis (PD) patients with PTH > or =300 pg/ml despite traditional therapy. A total of 395 patients received once-daily oral cinacalcet (260 HD, 34 PD) or placebo (89 HD, 12 PD) titrated from 30 to 180 mg to achieve a target intact PTH (iPTH) level of < or =250 pg/ml. During a 10-wk efficacy assessment phase, cinacalcet was more effective than control for PTH reduction outcomes, including proportion of patients with mean iPTH levels < or =300 pg/ml (46 versus 9%), proportion of patients with > or =30% reduction in iPTH from baseline (65 versus 13%), and proportion of patients with > or =20, > or =40, or > or =50% reduction from baseline. Cinacalcet had comparable efficacy in HD and PD patients; 50% of PD patients achieved a mean iPTH < or =300 pg/ml. Cinacalcet also significantly reduced serum calcium, phosphorus, and Ca x P levels compared with control treatment. The most common side effects, nausea and vomiting, were usually mild to moderate in severity and transient. Once-daily oral cinacalcet was effective in rapidly and safely reducing PTH, Ca x P, calcium, and phosphorus levels in patients who received HD or PD. Cinacalcet offers a new therapeutic option for controlling secondary hyperparathyroidism in patients with chronic kidney disease on dialysis.
传统疗法治疗继发性甲状旁腺功能亢进具有挑战性。拟钙剂西那卡塞盐酸盐作用于钙敏感受体,以增加其对钙的敏感性,从而减少甲状旁腺激素(PTH)分泌。这项3期、多中心、随机、安慰剂对照、双盲研究评估了西那卡塞在接受传统治疗但甲状旁腺激素水平≥300 pg/ml的血液透析(HD)和腹膜透析(PD)患者中的疗效和安全性。共有395例患者每日口服一次西那卡塞(260例HD患者,34例PD患者)或安慰剂(89例HD患者,12例PD患者),剂量从30 mg滴定至180 mg,以达到目标完整PTH(iPTH)水平≤250 pg/ml。在为期10周的疗效评估阶段,西那卡塞在降低PTH方面比对照组更有效,包括平均iPTH水平≤300 pg/ml的患者比例(46%对9%)、iPTH较基线水平降低≥30%的患者比例(65%对13%)以及较基线水平降低≥20%、≥40%或≥50%的患者比例。西那卡塞在HD和PD患者中的疗效相当;50%的PD患者平均iPTH≤300 pg/ml。与对照治疗相比,西那卡塞还显著降低了血清钙、磷和钙磷乘积水平。最常见的副作用恶心和呕吐通常严重程度为轻至中度且为一过性。每日口服一次西那卡塞可有效、安全地降低接受HD或PD治疗患者的PTH、钙磷乘积、钙和磷水平。西那卡塞为控制透析的慢性肾病患者的继发性甲状旁腺功能亢进提供了一种新的治疗选择。