Department of Pediatrics, Faculty of Medicine, University of Ottawa, Ottawa, Ontario K1H 8L1, Canada.
Shriners Hospitals for Children, Canada, McGill University, Montreal, Quebec H4A OA9, Canada.
J Clin Endocrinol Metab. 2022 Jul 14;107(8):e3241-e3253. doi: 10.1210/clinem/dgac296.
Younger age at treatment onset with conventional therapy (phosphate salts and active vitamin D; Pi/D) is associated with improved growth and skeletal outcomes in children with X-linked hypophosphatemia (XLH). The effect of age on burosumab efficacy and safety in XLH is unknown.
This work aimed to explore the efficacy and safety of burosumab vs Pi/D in younger (< 5 years) and older (5-12 years) children with XLH.
This post hoc analysis of a 64-week, open-label, randomized controlled study took place at 16 academic centers. Sixty-one children aged 1 to 12 years with XLH (younger, n = 26; older, n = 35) participated. Children received burosumab starting at 0.8 mg/kg every 2 weeks (younger, n = 14; older, n = 15) or continued Pi/D individually titrated per recommended guidelines (younger, n = 12; older, n = 20). The main outcome measure included the least squares means difference (LSMD) in Radiographic Global Impression of Change (RGI-C) rickets total score from baseline to week 64.
The LSMD in outcomes through 64 weeks on burosumab vs conventional therapy by age group were as follows: RGI-C rickets total score (younger, +0.90; older, +1.07), total Rickets Severity Score (younger, -0.86; older, -1.44), RGI-C lower limb deformity score (younger, +1.02; older, +0.91), recumbent length or standing height Z-score (younger, +0.20; older, +0.09), and serum alkaline phosphatase (ALP) (younger, -31.15% of upper normal limit [ULN]; older, -52.11% of ULN). On burosumab, dental abscesses were not reported in younger children but were in 53% of older children.
Burosumab appears to improve outcomes both in younger and older children with XLH, including rickets, lower limb deformities, growth, and ALP, compared with Pi/D.
与传统治疗(磷酸盐盐和活性维生素 D;Pi/D)相比,X 连锁低磷血症(XLH)患儿的治疗起始年龄较小与生长和骨骼结局改善有关。年龄对 XLH 中布罗索尤单抗疗效和安全性的影响尚不清楚。
本研究旨在探讨布罗索尤单抗与 Pi/D 在年龄较小(<5 岁)和年龄较大(5-12 岁)的 XLH 患儿中的疗效和安全性。
这是一项为期 64 周、开放标签、随机对照研究的事后分析,在 16 个学术中心进行。61 名年龄在 1 至 12 岁的 XLH 患儿(年龄较小者,n=26;年龄较大者,n=35)参与了本研究。患儿每 2 周接受 0.8mg/kg 的布罗索尤单抗起始治疗(年龄较小者,n=14;年龄较大者,n=15),或继续个体化滴定 Pi/D,按照推荐指南进行(年龄较小者,n=12;年龄较大者,n=20)。主要观察指标包括从基线到 64 周时放射学整体变化印象(RGI-C)佝偻病总评分的最小二乘均数差值(LSMD)。
按年龄组划分,64 周时布罗索尤单抗与传统疗法相比,各结局的 LSMD 如下:RGI-C 佝偻病总评分(年龄较小者,+0.90;年龄较大者,+1.07)、佝偻病总严重程度评分(年龄较小者,-0.86;年龄较大者,-1.44)、RGI-C 下肢畸形评分(年龄较小者,+1.02;年龄较大者,+0.91)、卧位或立位身长 Z 评分(年龄较小者,+0.20;年龄较大者,+0.09)和血清碱性磷酸酶(ALP)(年龄较小者,高于正常上限[ULN]的 31.15%;年龄较大者,高于 ULN 的 52.11%)。在年龄较小的患儿中,未报告布罗索尤单抗相关的牙脓肿,但在 53%的年龄较大的患儿中报告了该并发症。
与 Pi/D 相比,布罗索尤单抗似乎可改善 XLH 患儿的结局,包括佝偻病、下肢畸形、生长和 ALP,且在年龄较小和年龄较大的患儿中均有效。