Literature review and expert opinion on the impact of achondroplasia on medical complications and health-related quality of life and expectations for long-term impact of vosoritide: a modified Delphi study
Authors:
- Ravi SavarirayanRSRavi Savarirayan
- Wagner BaratelaWBWagner Baratela
- Thomas ButtTBThomas Butt
- Valérie Cormier-DaireVCValérie Cormier-Daire
- Melita IrvingMIMelita Irving
- Bradley S. MillerBMBradley S. Miller
- Klaus MohnikeKMKlaus Mohnike
- Keiichi OzonoKOKeiichi Ozono
- Ron RosenfeldRRRon Rosenfeld
- Angelo SelicorniASAngelo Selicorni
- Dominic ThompsonDTDominic Thompson
- Klane K. WhiteKWKlane K. White
Open Access
- 13 June 2022
- journal article
- review article
- Published by Springer Nature in Orphanet Journal of Rare Diseases
- Vol. 17 (1) , 1-10
Abstract
Background: 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. Results: 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%). Conclusions: 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.Keywords
Funding Information
- BioMarin Pharmaceutical (No award number)
This publication has 27 references indexed in Scilit:
- Current knowledge of medical complications in adults with achondroplasia: A scoping reviewClinical Genetics, 2019
- Physical, Mental, and Social Problems of Adolescent and Adult Patients with AchondroplasiaCalcified Tissue International, 2019
- Cervical spinal cord compression in infants with achondroplasia: should neuroimaging be routine?Genetics in Medicine, 2019
- Achondroplasia: a comprehensive clinical reviewOrphanet Journal of Rare Diseases, 2019
- The prevalence of the complications and their associated factors in humeral lengthening for achondroplasia: retrospective study of 54 casesJournal of Pediatric Orthopaedics B, 2017
- Sleep‐disordered breathing and its management in children with achondroplasiaAmerican Journal of Medical Genetics Part A, 2017
- Neutral Endopeptidase-Resistant C-Type Natriuretic Peptide Variant Represents a New Therapeutic Approach for Treatment of Fibroblast Growth Factor Receptor 3–Related DwarfismThe Journal of Pharmacology and Experimental Therapeutics, 2015
- Evaluation of the Therapeutic Potential of a CNP Analog in a Fgfr3 Mouse Model Recapitulating AchondroplasiaThe American Journal of Human Genetics, 2012
- Cross‐sectional assessment of pain and physical function in skeletal dysplasia patientsClinical Genetics, 2012
- Physeal growth arrest after tibial lengthening in achondroplasiaActa Orthopaedica, 2012