Comparative Effectiveness of Calcimimetic Agents for Secondary Hyperparathyroidism in Adults: A Systematic Review and Network Meta-analysis

被引:46
作者
Palmer, Suetonia C. [1 ]
Mavridis, Dimitris [2 ,3 ]
Johnson, David W. [4 ]
Tonelli, Marcello [5 ]
Ruospo, Marinella [6 ]
Strippoli, Giovanni F. M. [6 ,7 ]
机构
[1] Univ Otago Christchurch, Christchurch, New Zealand
[2] Univ Ioannina, Dept Primary Educ, Ioannina, Greece
[3] Paris Descartes Univ, Paris, France
[4] Univ Queensland, Princess Alexandra Hosp, St Lucia, Qld, Australia
[5] Univ Calgary, Cumming Sch Med, Calgary, AB, Canada
[6] Univ Bari, Dept Emergency & Organ Transplantat, Piazza Giulio Cesare, I-70124 Bari, Italy
[7] Univ Sydney, Sydney Sch Publ Hlth, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
PATIENTS RECEIVING HEMODIALYSIS; CARDIOVASCULAR-DISEASE; PARATHYROID-HORMONE; DOUBLE-BLIND; CINACALCET; ETELCALCETIDE; HETEROGENEITY; EFFICACY; THERAPY; PLACEBO;
D O I
10.1053/j.ajkd.2020.02.439
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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. Study Design: 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 metaanalysis. Data Extraction: 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. Analytical Approach: Frequentist network metaanalysis 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. Results: 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. Limitations: Lack of longer-term data; heterogeneous end point definitions. Conclusions: 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.
引用
收藏
页码:321 / 330
页数:10
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