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X 连锁低磷血症患儿接受布罗索尤单抗治疗后的线性生长:一项真实世界观察性研究。

Linear growth of children with X-linked hypophosphatemia treated with burosumab: a real-life observational study.

机构信息

Pediatric Endocrinology Unit, The Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Center, Tel Hashomer, 52621, Israel.

The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

Eur J Pediatr. 2023 Nov;182(11):5191-5202. doi: 10.1007/s00431-023-05190-y. Epub 2023 Sep 14.

Abstract

UNLABELLED

To assess the long-term efficacy of burosumab for pediatric patients with X-linked hypophosphatemia, focusing on linear growth. This multi-center retrospective study included 35 pediatric patients who began treatment with burosumab between January 2018 and January 2021. We collected clinical data, anthropometric measurements, laboratory results, and Rickets Severity Score (RSS), from 2 years prior to treatment initiation and up to 4 years after. Burosumab was initiated at a mean age of 7.5 ± 4.4 years (range 0.6-15.9), with a mean initial dose of 0.8 ± 0.3 mg/kg, which was subsequently increased to 1.1 ± 0.4 mg/kg. The patients were followed for 2.9 ± 1.4 years (range 1-4) after initiating burosumab. Serum phosphorus levels increased from 2.7 ± 0.8 mg/dl at burosumab initiation to 3.4 ± 0.6 mg/dl after 3 months and remained stable (p < 0.001). Total reabsorption of phosphorus increased from 82.0 ± 6.8 to 90.1 ± 5.3% after 12 months of treatment (p = 0.041). The RSS improved from 1.7 ± 1.0 at burosumab initiation to 0.5 ± 0.6 and 0.3 ± 0.6 after 12 and 24 months, respectively (p < 0.001). Both height z-score and weight z-score improved from burosumab initiation to the end of the study: from - 2.07 ± 1.05 to - 1.72 ± 1.04 (p < 0.001) and from - 0.51 ± 1.12 to - 0.11 ± 1.29 (p < 0.001), respectively. Eight children received growth hormone combined with burosumab treatment. Height z-score improved among those who received growth hormone (from - 2.33 ± 1.12 to - 1.94 ± 1.24, p = 0.042) and among those who did not (from - 2.01 ± 1.01 to - 1.66 ± 1.01, p = 0.001).

CONCLUSION

Burosumab treatment in a real-life setting improved phosphate homeostasis and rickets severity and enhanced linear growth.

WHAT IS KNOWN

• Compared to conventional therapy, burosumab treatment has been shown to increase serum phosphate levels and reduce the severity of rickets. • The effect of burosumab on growth is still being study.

WHAT IS NEW

• Height z-score improved between the start of burosumab treatment and the end of the study (-2.07 ± 1.05 vs. -1.72 ± 1.04, p < 0.001). • Eight children received burosumab combined with growth hormone treatment without side effects during the concomitant treatments.

摘要

目的

评估布罗索尤单抗治疗 X 连锁低磷血症患儿的长期疗效,重点关注线性生长。方法:这是一项多中心回顾性研究,纳入了 2018 年 1 月至 2021 年 1 月期间开始接受布罗索尤单抗治疗的 35 名儿科患者。我们收集了治疗前 2 年和治疗后 4 年的临床数据、人体测量数据、实验室结果和佝偻病严重程度评分(RSS)。布罗索尤单抗的起始剂量为 0.8±0.3mg/kg,平均年龄为 7.5±4.4 岁(范围 0.6-15.9),随后增加至 1.1±0.4mg/kg。患者在开始布罗索尤单抗治疗后平均随访 2.9±1.4 年(范围 1-4 年)。治疗 3 个月后,血清磷水平从 2.7±0.8mg/dl 升高至 3.4±0.6mg/dl(p<0.001),并保持稳定。治疗 12 个月后,总磷吸收率从 82.0±6.8%增加至 90.1±5.3%(p=0.041)。RSS 从布罗索尤单抗起始时的 1.7±1.0 分别改善至 12 个月时的 0.5±0.6 和 24 个月时的 0.3±0.6(p<0.001)。身高 z 评分和体重 z 评分均从布罗索尤单抗起始时改善至研究结束时:从-2.07±1.05 改善至-1.72±1.04(p<0.001)和从-0.51±1.12 改善至-0.11±1.29(p<0.001)。8 名儿童接受了生长激素联合布罗索尤单抗治疗。接受生长激素治疗的儿童身高 z 评分有所改善(从-2.33±1.12 改善至-1.94±1.24,p=0.042),而未接受生长激素治疗的儿童身高 z 评分也有所改善(从-2.01±1.01 改善至-1.66±1.01,p=0.001)。结论:布罗索尤单抗治疗可改善低磷血症患儿的磷酸盐稳态和佝偻病严重程度,并促进线性生长。

已知

与传统疗法相比,布罗索尤单抗治疗可提高血清磷酸盐水平并降低佝偻病的严重程度。布罗索尤单抗对生长的影响仍在研究中。

新发现

治疗开始至研究结束时,身高 z 评分改善(从-2.07±1.05 改善至-1.72±1.04,p<0.001)。8 名儿童接受了布罗索尤单抗联合生长激素治疗,在联合治疗期间无副作用。

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