Suppr超能文献

布罗索尤单抗对X连锁低磷血症患儿下肢对线的影响。

Impact of burosumab on lower limb alignment in children with X-linked hypophosphatemia.

作者信息

Frumberg David B, Merritt J Lawrence, Chen Angel, Carpenter Thomas O

机构信息

Department of Orthopaedics and Rehabilitation, Yale University School of Medicine, New Haven, CT, USA.

Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.

出版信息

J Pediatr Soc North Am. 2024 Feb 28;6:100012. doi: 10.1016/j.jposna.2024.100012. eCollection 2024 Feb.

Abstract

BACKGROUND

Osteotomy and hemiepiphysiodesis are used to treat lower limb deformities in the rare musculoskeletal disease X-linked hypophosphatemia (XLH), but postsurgical complications and malalignment recurrence are possible. This retrospective analysis assessed whether treatment with burosumab, a fully human IgG1 monoclonal antibody to fibroblast growth factor 23 approved for treatment of rickets in XLH, improves lower limb malalignment toward age-specific normal values in children with XLH.

METHODS

Children with confirmed XLH received burosumab for 160 weeks in the open-label phase 2 study CL205, or conventional therapy (Pi/D) or burosumab for 64 weeks in the randomized, open-label phase 3 study CL301, with crossover from Pi/D to burosumab through 88 weeks. Full-length, anteroposterior lower limb radiographs were reviewed. The mechanical femoral-tibial angle (MFTA) of lower limbs was measured at baseline and postbaseline. Each MFTA was classified as normal (within 1 standard deviation [SD] of age-specific normal range) or clinically normal (within 2 degrees of normal).

RESULTS

Overall, 116 limbs were included (CL205,  = 26; CL301,  = 90). Varus or valgus limbs were observed at baseline in 21 (80.8%) limbs in CL205 and in 69 (76.7%) limbs in CL301. In CL205, mean (SD) MFTA decreased from 13.0° (6.7°) at baseline to 5.7° (6.0°) at week 64 and 1.0° (4.8°) at week 160. In CL301, mean (SD) MFTA decreased from 15.5° (13.6°) at baseline to 8.5° (10.0°) at week 64 in the burosumab arm, and in the crossover arm, from 9.2° (10.4°) at week 64 to 6.9° (9.4°) at week 88 (after 22 weeks of burosumab). The proportion of normal or clinically normal limbs increased with burosumab in CL205 (baseline to week 160, 19.2% to 58.3%) and in the CL301 burosumab arm (baseline to week 64, 19.6% to 37.0%) but not in the CL301 crossover arm (week 64-88, 34.1% to 33.3%).

CONCLUSIONS

In children with XLH, long-term treatment with burosumab is capable of correcting the MFTA of varus and valgus lower limbs to a neutral alignment without requiring surgical intervention.

KEY CONCEPTS

1.Treatment with burosumab led to the correction of lower limb angular deformity to neutral alignment in children with X-linked hypophosphatemia (XLH).2.Continued treatment with burosumab for at least 1 year appears to have further positive effects on the correction of lower limb angular deformity in children with XLH.3.Initial treatment with burosumab is indicated in young children with XLH for whom hemiepiphysiodesis is being considered.

LEVEL OF EVIDENCE

III.

摘要

背景

截骨术和半骨骺阻滞术用于治疗罕见的肌肉骨骼疾病X连锁低磷血症(XLH)中的下肢畸形,但术后可能出现并发症和畸形复发。这项回顾性分析评估了布罗索尤单抗(一种已获批用于治疗XLH患儿佝偻病的抗成纤维细胞生长因子23的全人IgG1单克隆抗体)治疗是否能使XLH患儿的下肢畸形向年龄特异性正常值改善。

方法

确诊为XLH的患儿在开放标签的2期研究CL205中接受布罗索尤单抗治疗160周,或在随机、开放标签的3期研究CL301中接受传统治疗(磷/维生素D)或布罗索尤单抗治疗64周,并在88周内从磷/维生素D交叉至布罗索尤单抗治疗。回顾下肢全长前后位X线片。在基线和基线后测量下肢的机械股胫角(MFTA)。每个MFTA被分类为正常(在年龄特异性正常范围的1个标准差[SD]内)或临床正常(在正常范围的2度内)。

结果

总共纳入116条肢体(CL205组26条;CL301组90条)。CL205组21条(80.8%)肢体和CL301组69条(76.7%)肢体在基线时观察到内翻或外翻。在CL205组中,平均(SD)MFTA从基线时的13.0°(6.7°)降至第64周时的5.7°(6.0°)和第160周时的1.0°(4.8°)。在CL301组中,布罗索尤单抗治疗组的平均(SD)MFTA从基线时的15.5°(13.6°)降至第64周时的8.5°(10.0°),在交叉治疗组中,从第64周时的9.2°(10.4°)降至第88周时的6.9°(9.4°)(布罗索尤单抗治疗22周后)。CL205组(从基线到第160周,19.2%至58.3%)和CL301组布罗索尤单抗治疗组(从基线到第64周,19.6%至37.0%)中正常或临床正常肢体的比例随布罗索尤单抗治疗增加,但CL301组交叉治疗组中未增加(第64 - 88周,34.1%至33.3%)。

结论

在XLH患儿中,长期使用布罗索尤单抗能够将内翻和外翻下肢的MFTA矫正至中立位排列,而无需手术干预。

关键概念

1.布罗索尤单抗治疗可使X连锁低磷血症(XLH)患儿的下肢角畸形矫正至中立位排列。2.持续使用布罗索尤单抗治疗至少1年似乎对XLH患儿下肢角畸形的矫正有进一步的积极作用。3.对于正在考虑半骨骺阻滞术的年幼XLH患儿,建议初始使用布罗索尤单抗治疗。

证据级别

III级

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验