首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >A randomized, double-blind, placebo-controlled study to assess the efficacy and safety of cinacalcet HCl in participants with CKD not receiving dialysis.
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A randomized, double-blind, placebo-controlled study to assess the efficacy and safety of cinacalcet HCl in participants with CKD not receiving dialysis.

机译:一项随机,双盲,安慰剂对照研究,用于评估盐酸西那卡塞对未接受透析的CKD参与者的疗效和安全性。

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BACKGROUND: Secondary hyperparathyroidism is observed in patients with early chronic kidney disease (CKD). This study investigated the safety and efficacy of cinacalcet for secondary hyperparathyroidism in participants with CKD not receiving dialysis. STUDY DESIGN: Double-blind, randomized, 32-week, phase 3 study. SETTING & PARTICIPANTS: 404 participants with stage 3 or 4 CKD from 73 centers in 9 countries. INTERVENTIONS: Cinacalcet:placebo (3:1 ratio). OUTCOMES & MEASUREMENTS: Proportion of participants with a mean decrease of 30% or greater in intact parathyroid hormone (iPTH) level, proportion with iPTH level of 70 or less or 110 or less pg/mL (stage 3 and 4 CKD, respectively), and mean percentage of iPTH change from baseline, all during the efficacy-assessment phase. RESULTS: A greater proportion of cinacalcet than placebo participants achieved a 30% or greater decrease in iPTH level (74% versus 28%; P < 0.001), corresponding to a 43.1% decrease in iPTH level from baseline (cinacalcet) compared with a 1.1% increase (placebo). At week 32, serum calcium levels were 8.9 +/- 0.8 mg/dL (-8.9%; cinacalcet) and 9.9 +/- 0.6 mg/dL (+0.8%; placebo), phosphorus levels were 4.5 +/- 1.0 mg/dL (+21.4%) and 4.0 +/- 0.7 mg/dL (+6.8%), and calcium-phosphorus product values were 40.1 +/- 8.3 mg(2)/dL(2) (+18.9%) and 38.9 +/- 6.9 mg(2)/dL(2) (+17.1%), respectively. During the study course, 62% (cinacalcet) and 1% (placebo) of participants experienced 2 consecutive serum calcium concentrations less than 8.4 mg/dL. They generally were asymptomatic and without significant clinical consequences. Treatment generally was well tolerated, and most adverse events were mild to moderate in severity. LIMITATIONS: The study was not designed to assess the effects of cinacalcet on vascular calcification, bone histomorphometric parameters, or other clinical outcomes. It is not known whether the observed differences in changes in iPTH levels are clinically more important than observed differences in changes in serum calcium or phosphorus levels or dosages of vitamin D sterols and phosphate binders. CONCLUSIONS: These data show that cinacalcet treatment in patients with CKD not receiving dialysis can decrease plasma iPTH levels, but with frequent (albeit generally asymptomatic) serum calcium levels less than 8.4 mg/dL and increases in serum phosphorus levels.
机译:背景:在患有早期慢性肾脏病(CKD)的患者中观察到继发性甲状旁腺功能亢进。这项研究调查了西那卡塞对未接受透析的CKD参与者继发性甲状旁腺功能亢进的安全性和有效性。研究设计:双盲,随机,32周的3期研究。参加者和参与者:来自9个国家/地区的73个中心的404名参与者处于CKD的第3或第4阶段。干预措施:西那卡塞:安慰剂(比例为3:1)。结果与测量:完整甲状旁腺激素(iPTH)水平平均降低30%或更多,平均iPTH水平为70或更低或110或更低pg / mL的参与者所占比例(分别为CKD的第三阶段和第四阶段),以及iPTH相对于基线的平均变化百分比,所有这些都在疗效评估阶段进行。结果:与安慰剂参与者相比,西那卡塞的比例更大,其iPTH水平降低了30%或更高(74%比28%; P <0.001),与基线(西那卡塞)相比iPTH水平降低了43.1%,而后者为1.1增加百分比(安慰剂)。在第32周时,血清钙水平为8.9 +/- 0.8 mg / dL(-8.9%;西那卡塞)和9.9 +/- 0.6 mg / dL(+ 0.8%;安慰剂),磷水平为4.5 +/- 1.0 mg / d dL(+ 21.4%)和4.0 +/- 0.7 mg / dL(+ 6.8%),钙磷产物值为40.1 +/- 8.3 mg(2)/ dL(2)(+ 18.9%)和38.9 +分别为6.9 mg(2)/ dL(2)(+ 17.1%)。在研究过程中,有62%(西那卡塞)和1%(安慰剂)的参与者连续2次血清钙浓度低于8.4 mg / dL。它们通常是无症状的,没有明显的临床后果。一般而言,治疗耐受性良好,大多数不良事件的严重程度为轻度至中度。局限性:该研究并非旨在评估西那卡塞对血管钙化,骨组织形态学参数或其他临床结果的影响。在临床上,观察到的iPTH水平变化的差异是否比观察到的血清钙或磷水平或维生素D固醇和磷酸盐结合剂的剂量变化的差异更重要,这一点尚不清楚。结论:这些数据表明,未接受透析的CKD患者使用西那卡塞治疗可降低血浆iPTH水平,但经常(尽管通常无症状)血清钙水平低于8.4 mg / dL,且血清磷水平升高。

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