Murdoch Children's Research Institute, and University of Melbourne, Parkville, Melbourne, VIC, 3052, Australia.
Hospital Sirio-Libanes, São Paolo, Brazil.
Orphanet J Rare Dis. 2022 Jun 13;17(1):224. doi: 10.1186/s13023-022-02372-z.
Achondroplasia is associated with disproportionate short stature and significant and potentially severe medical complications. Vosoritide is the first medicine to treat the underlying cause of achondroplasia and data from phase 3 and phase 2 extension studies showed effects on growth and body proportions. However, there are currently no long-term data available on the direct impact on endpoints such as medical complications and health-related quality of life (HRQoL). This study explored the perceived impact of achondroplasia on medical complications, HRQoL, healthcare resource use and mortality, and potential modifying effects of vosoritide, based on published evidence and expert opinion. Structured expert opinion was obtained by an international modified Delphi study among 14 experts in managing achondroplasia performed on a virtual platform and consisting of an explorative phase followed by an anonymous individual rating round.
Overall, the panelists expect that in individuals starting long-term treatment between 2 years of age and puberty, growth velocity increases observed in the clinical trials will be maintained until final height is reached (92% agreement) and will likely result in clinically meaningful improvements in upper-to-lower body segment ratio (85%). Earlier treatment initiation will likely result in a greater final height (100%) and more likely improve proportionality (92%) than later treatment. Although current data are limited, ≥ 75% of panelists find it conceivable that the earlier long-term treatment is started, the greater the probability of a positive effect on the lifetime incidence of symptomatic spinal stenosis, kyphosis, obstructive sleep apnea, and foramen magnum stenosis. These are among the most clinically important complications of achondroplasia because of their high impact on comorbidity, mortality, and/or HRQoL. A positive effect of vosoritide on the incidence of surgeries through lifetime was considered more likely with earlier long-term treatment (90%).
This explorative study, based on international expert opinion, provides further insight into the medical and functional impacts of achondroplasia and how these might be modified through long-term use of vosoritide. The results can be used to guide the direction and design of future research to validate the assumptions and to discuss potential treatment outcomes with disease modifying therapies with families and clinicians.
软骨发育不全症与不成比例的身材矮小以及严重且潜在的医疗并发症有关。Vosoritide 是第一种治疗软骨发育不全症根本原因的药物,来自 3 期和 2 期扩展研究的数据表明其对生长和身体比例有影响。然而,目前尚无关于终点(如医疗并发症和健康相关生活质量 (HRQoL))的直接影响的长期数据。本研究基于已发表的证据和专家意见,探讨了软骨发育不全症对医疗并发症、HRQoL、医疗资源使用和死亡率的影响,以及 vosoritide 的潜在调节作用。通过在虚拟平台上对 14 名软骨发育不全症管理专家进行的国际改良 Delphi 研究,获得了结构化的专家意见,该研究由探索阶段和匿名个人评分轮次组成。
总体而言,专家小组预计,在 2 岁至青春期开始长期治疗的个体中,临床试验中观察到的生长速度将保持到最终身高(92%的共识),并且可能导致上半身与下半身比例的临床意义上的改善(85%)。早期治疗开始可能会导致最终身高更高(100%),并且更有可能改善比例(92%),而晚期治疗则不然。尽管目前的数据有限,但专家小组中有≥75%的人认为,早期长期治疗开始得越早,对终身出现症状性脊柱狭窄、后凸、阻塞性睡眠呼吸暂停和枕骨大孔狭窄的概率就越大。这些是软骨发育不全症中最具临床意义的并发症之一,因为它们对合并症、死亡率和/或 HRQoL 有很高的影响。早期长期治疗更有可能对终身手术发生率产生积极影响(90%)。
本探索性研究基于国际专家意见,进一步深入了解了软骨发育不全症的医疗和功能影响,以及通过长期使用 vosoritide 如何对其进行调节。研究结果可用于指导未来研究的方向和设计,验证假设,并与家庭和临床医生讨论潜在的疾病修饰治疗的治疗结果。