Postgraduate Program "Research Methodology in Medicine and Health Sciences", Aristotle University of Thessaloniki, Thessaloniki, Greece.
School of Medicine, Faculty of Health Science, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Calcif Tissue Int. 2024 Sep;115(3):229-241. doi: 10.1007/s00223-024-01250-z. Epub 2024 Jul 15.
To assess the efficacy and safety of burosumab in children and adults with X-linked hypophosphatemia based on real-world evidence. MEDLINE (via PubMed) and Cochrane Library were searched until 18 October 2023 for single-arm (before-after) studies. Registries including Clinicaltrials.gov, EU Clinical Trials, WHO International Clinical Trials Registry Platform, and conference abstracts. The outcomes were a change in serum phosphorus concentrations and change in RSS, a change in serum ALP, bone-specific ALP, a change in the ratio of Tubular maximum reabsorption of Phosphate to Glomerular Filtrate rate, a change in serum 1,25(OH)D and 25(OH)D concentrations, change in height Z-score, McMaster Universities Osteoarthritis Index (WOMAC) and safety outcomes. An inverse variance random-effects meta-analysis was applied for data synthesis. Fifteen studies (289 participants) were included. Burosumab treatment improved serum phosphate concentrations [mean difference 0.88 mg/dl, 95% confidence interval 0.70 to 1.07, I = 92%), Rickets Severity score (mean difference - 1.86, 95% confidence interval - 2.5 to - 1.21, I = 71%), serum alkaline phosphate concentrations (mean difference - 1.86, 95% confidence interval - 2.5 to - 1.21, I = 71%), serum 1,25(OH)D concentrations (mean difference 18.91 pg/ml, 95% confidence interval 6.39 to 31.43, I = 96%) and renal phosphate reabsorption (mean difference 1.22 mg/dl, 95% confidence interval 0.70 to 1.74, I 93%). Burosumab treatment improved overall clinical and laboratory findings in patients with X-linked hypophosphatemia.
评估基于真实世界证据的布罗索尤单抗在 X 连锁低磷血症儿童和成人中的疗效和安全性。检索 MEDLINE(通过 PubMed)和 Cochrane Library,截至 2023 年 10 月 18 日,检索单臂(前后)研究。注册包括 Clinicaltrials.gov、EU Clinical Trials、WHO 国际临床试验注册平台和会议摘要。结局指标为血清磷浓度变化和 RSS 变化、血清碱性磷酸酶变化、骨特异性碱性磷酸酶变化、肾小管最大磷重吸收与肾小球滤过率比值变化、血清 1,25(OH)D 和 25(OH)D 浓度变化、身高 Z 评分变化、麦克马斯特大学骨关节炎指数(WOMAC)和安全性结局。应用逆方差随机效应荟萃分析进行数据综合。纳入了 15 项研究(289 名参与者)。布罗索尤单抗治疗可改善血清磷浓度[平均差 0.88mg/dl,95%置信区间 0.70 至 1.07,I=92%]、佝偻病严重程度评分[平均差-1.86,95%置信区间-2.5 至-1.21,I=71%]、血清碱性磷酸酶浓度[平均差-1.86,95%置信区间-2.5 至-1.21,I=71%]、血清 1,25(OH)D 浓度[平均差 18.91pg/ml,95%置信区间 6.39 至 31.43,I=96%]和肾磷重吸收[平均差 1.22mg/dl,95%置信区间 0.70 至 1.74,I93%]。布罗索尤单抗治疗可改善 X 连锁低磷血症患者的整体临床和实验室发现。