Evidence map›Paper›PMID 40676599›Full record

ArticleOrphanet journal of rare diseases2025

Integrating vosoritide therapy with limb surgery in paediatric patients with achondroplasia: real-life experiences.

Anna Elsa Maria Allegri, Maria Francesca Bedeschi, Maria Beatrice Bocchi, Valentina Camurri, Michaela Veronika Gonfiantini, Chiara Leoni, Milena Mariani, Osvaldo Palmacci, Matteo Porro, Simone Riganti and 10 more

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Patient perspectives on humeral lengthening in achondroplasia: association between treatment timing and acceptance.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2026
    Article
  5. C-Type Natriuretic Peptide Derivatives: Orthopaedic Implications in Achondroplasia.Journal of the Pediatric Orthopaedic Society of North America · 2026
    Review
  6. Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Anna Elsa Maria Allegri *Paediatric Endocrinology Unit, Department of Paediatrics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Maria Francesca Bedeschi *Medical Genetic Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy. mariafrancesca.bedeschi@policlinico.mi.it.ORCID http://orcid.org/0000-0002-6723-9177
Maria Beatrice BocchiDepartment of Orthopaedics and Traumatology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, Roma, Italy.
Valentina CamurriDepartment of Paediatric Orthopaedics, IRCCS Giannina Gaslini, Genoa, Italy.
Michaela Veronika GonfiantiniRare Diseases and Medical Genetics Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Chiara LeoniCenter for Rare Diseases, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.
Milena MarianiPaediatric Unit ASST Lariana, Mariani foundation Center for fragile Child, Como, Italy.
Osvaldo PalmacciDepartment of Orthopaedics and Traumatology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, Roma, Italy.
Matteo PorroPaediatric Physical Medicine and Rehabilitation Service, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Simone RigantiDepartment of Paediatric Orthopaedics, IRCCS Giannina Gaslini, Genoa, Italy.
Caterina TedescoPaediatric Endocrinology Unit, Department of Paediatrics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Berardo RinaldiMedical Genetic Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.
Emanuela ScaranoPaediatric Physical Medicine and Rehabilitation Service, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Concetta SchiavarielloPaediatric Physical Medicine and Rehabilitation Service, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Angelo SelicorniPaediatric Unit ASST Lariana, Mariani foundation Center for fragile Child, Como, Italy.
Stefano StagiDepartment of Health Sciences, University of Florence, Florence, Italy.
Fabio VerdoniIRCCS Ospedale Galeazzi Sant'Ambrogio, Milan, Italy.
Giuseppe ZampinoCenter for Rare Diseases, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.
Mohamad MaghniePaediatric Endocrinology Unit, Department of Paediatrics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Roberta OnesimoCenter for Rare Diseases, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.

Funding

BioMarin Pharmaceutical NoneENDO ERN and ERN BOND - European Reference Network for rare Bone Diseases ENDO ERN and ERN BOND - European Reference Network for rare Bone Diseases
6 · The paper itself

Abstract

backgroundAchondroplasia is the most common form of disproportionate short stature and can lead to serious medical complications, including foramen magnum and spinal stenosis. Until 2021, there were no precision treatments available, and in some countries, elective surgery was considered a standard approach to increase height, improve body proportions, enhance functionality, and correct deformities in a selected group of patients. Recently, C-type natriuretic peptide (CNP) has been explored as a potential treatment, aiming to counteract the molecular activity driven by FGFR3. Although post-market and real-world data on the drug are still limited, many questions remain about the potential for combining pharmacological and surgical therapies and how this might influence patient outcomes. Concerns have also been raised regarding the potential impact of drugs on bone healing. However, anecdotal evidence from orthopaedic practice suggests that the two ossification processes do not interfere with one another. The aim of this study was to describe the first real-world case series in which vosoritide treatment was integrated with limb surgery in children and adolescents with achondroplasia.

resultsSixteen paediatric patients with molecular confirmation of achondroplasia were included in the study. All patients underwent combined vosoritide therapy and limb surgeries (13 for lower limb lengthening and 3 for varus correction through epiphysiodesis).The complementary roles of vosoritide therapy and surgery were highlighted, with treatment outcomes aligning closely with expectations.

conclusionThis report provides the first clinical description of the combination of precision therapy with limb surgery in a relatively large multicentre cohort of paediatric patients with achondroplasia. These findings support continued exploration of the integration of different therapeutic approaches.

Indexed as

AchondroplasiaNatriuretic Peptide, C-TypeAdolescentChildChild, PreschoolFemaleHumansMaleNatriuretic Peptide, C-TypevosoritideAchondroplasiaLower limb lengtheningSurgeryVosoritide

Identifiers

PMID40676599
PMCPMC12273278

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.