University of Otago Christchurch, Christchurch, New Zealand.
Department of Primary Education, University of Ioannina, Greece; Paris Descartes University, Paris, France.
Am J Kidney Dis. 2020 Sep;76(3):321-330. doi: 10.1053/j.ajkd.2020.02.439. Epub 2020 May 28.
RATIONALE & OBJECTIVE: Comparative benefits and harms of calcimimetic agents used for the treatment of secondary hyperparathyroidism have not been well characterized. We sought to compare the effectiveness of 3 calcimimetic agents using published data.
Systematic review of randomized controlled trials and network meta-analysis.
SETTING & STUDY POPULATION: Adults with chronic kidney disease enrolled in a clinical trial of a calcimetic agent.
SEARCH STRATEGY & SOURCES: MEDLINE, EMBASE, CENTRAL (from February 7, 2013, to November 21, 2019), and a published meta-analysis.
Two reviewers independently extracted the study data, assessed risk of bias, and rated evidence certainty using Grading of Recommendations Assessment, Development and Evaluation (GRADE) criteria.
Frequentist network meta-analysis was conducted. The primary review outcomes were achievement of a target reduction in serum parathyroid hormone (PTH) levels and hypocalcemia. Additional outcomes were nausea, vomiting, serious adverse events, all-cause mortality, cardiovascular mortality, heart failure, and fracture.
36 trials (11,247 participants) were included. All except 4 trials involved dialysis patients. Median follow-up was 26 weeks (range, 1 week to 21.2 months). Compared with placebo, calcimimetic agents had higher odds of achieving target PTH levels with high or moderate certainty. Etelcalcetide had the highest odds of achieving a PTH target compared with evocalcet (OR, 4.93; 95% CI, 1.33-18.2) and cinacalcet (OR, 2.78; 95% CI, 1.19-6.67). Etelcalcetide appeared to cause more hypocalcemia than cinacalcet and evocalcet. Cinacalcet and to a lesser extent etelcalcetide appeared to cause more nausea than placebo. Differences in risk for mortality, cardiovascular end points, or fractures across calcimimetic agents could not be discerned with sufficient certainty.
Lack of longer-term data; heterogeneous end point definitions.
Evidence of the benefits of calcimimetic therapy is limited to short-term assessment of a putative surrogate outcome (serum PTH). Although etelcalcetide was associated with the largest reduction in PTH levels, side-effect profiles differed across the 3 calcimimetic agents, making it not possible to identify 1 preferred agent.
用于治疗继发性甲状旁腺功能亢进的拟钙剂的相对益处和危害尚未得到充分描述。我们试图使用已发表的数据比较 3 种拟钙剂的有效性。
系统评价随机对照试验和网络荟萃分析。
参加拟钙剂临床试验的慢性肾脏病成年患者。
MEDLINE、EMBASE、CENTRAL(2013 年 2 月 7 日至 2019 年 11 月 21 日)和已发表的荟萃分析。
两位审查员独立提取研究数据,使用推荐评估、制定与评价(GRADE)标准评估偏倚风险并对证据确定性进行分级。
采用经典网络荟萃分析。主要评价结局为血清甲状旁腺激素(PTH)水平达标率和低钙血症发生率。其他结局为恶心、呕吐、严重不良事件、全因死亡率、心血管死亡率、心力衰竭和骨折。
纳入 36 项试验(11247 名参与者)。除 4 项试验外,其余均涉及透析患者。中位随访时间为 26 周(范围:1 周至 21.2 个月)。与安慰剂相比,拟钙剂更有可能实现 PTH 水平达标,其证据确定性为高或中。依特卡塞与埃卡塞特(OR,4.93;95%CI,1.33-18.2)和西那卡塞(OR,2.78;95%CI,1.19-6.67)相比,更有可能实现 PTH 达标。与西那卡塞和埃卡塞特相比,依特卡塞更易导致低钙血症。与安慰剂相比,西那卡塞和依特卡塞更易导致恶心。但无法确定拟钙剂之间的死亡率、心血管终点或骨折风险的差异是否具有足够的确定性。
缺乏长期数据;终点定义存在异质性。
拟钙剂治疗的益处证据仅限于对潜在替代结局(血清 PTH)的短期评估。尽管依特卡塞与 PTH 水平下降幅度最大相关,但 3 种拟钙剂的副作用谱不同,因此无法确定 1 种首选药物。