Evidence map›Paper›PMID 37882884›Full record

ArticleAdvances in therapy2024

Vosoritide Therapy in Children with Achondroplasia: Early Experience and Practical Considerations for Clinical Practice.

Oliver Semler, Valérie Cormier-Daire, Ekkehart Lausch, Michael B Bober, Ricki Carroll, Sérgio B Sousa, David Deyle, Maha Faden, Gabriele Hartmann, Aaron J Huser and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Advances in therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
8.5field-weighted citation impact, top 2% of its field
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

15 citing papers in PubMed, 27 citations in OpenAlex.

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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 at 18 institutions in 6 countries.

Oliver SemlerFaculty of Medicine, Center for Rare Diseases, University Hospital Cologne, University of Cologne, Cologne, Germany. joerg.semler@uk-koeln.de.ORCID 0000-0003-0029-7556
Valérie Cormier-DaireCentre of Reference for Constitutional Bone Diseases (MOC), Department of Clinical Genetics, Paris Centre University, INSERM UMR 1163, Imagine Institute, Necker-Enfants Malades Hospital, Paris, France.
Ekkehart LauschPediatric Genetics, Center for Pediatric and Adolescent Medicine, University Hospital Freiburg, Freiburg, Germany.
Michael B BoberNemours Skeletal Dysplasia Program, Nemours Children's Hospital, Delaware, Wilmington, DE, USA.ORCID 0000-0002-6178-1264
Ricki CarrollNemours Skeletal Dysplasia Program, Nemours Children's Hospital, Delaware, Wilmington, DE, USA.ORCID 0000-0002-9221-4879
Sérgio B SousaMedical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.ORCID 0000-0003-3921-1334
David DeyleDepartment of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
Maha FadenMedical Genetic Unit, Children's Hospital, King Saud Medical City, Riyadh, Saudi Arabia.
Gabriele HartmannVienna Bone and Growth Center, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
Aaron J HuserPaley Advanced Limb Lengthening Institute, West Palm Beach, FL, USA.
Janet M LegareDepartment of Pediatrics, School of Medicine and Public Health, University of Wisconsin, Madison, WI, USA.ORCID 0000-0001-6684-4909
Klaus MohnikeUniversitätskinderklinik, Otto-Von-Guericke Universität, Magdeburg, Germany.
Tilman R RohrerDepartment of General Pediatrics and Neonatology, Saarland University Medical Centre, Homburg, Germany.ORCID 0000-0001-9516-7863
Frank RutschDepartment of General Pediatrics, Münster University Children's Hospital, Münster, Germany.
Pamela SmithDivision of Endocrinology, Phoenix Children's Hospital, Phoenix, AZ, USA.ORCID 0000-0002-2588-9657
Andre M TravessaDepartment of Medical Genetics, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.ORCID 0000-0002-4147-2800
Angela VerardoDivision of Pediatric Endocrinology, Children's Hospital of New Jersey at Newark Beth Israel Medical Center, Newark, NJ, USA.
Klane K WhiteChildren's Hospital Colorado, Aurora, CO, USA.
William R WilcoxDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
Julie Hoover-FongDepartment of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0002-1242-5626
Alfred I. duPont Hospital for Children · USCentro Hospitalar Lisboa Norte · PTChildren's Hospital Colorado · USEmory University · USHospitais da Universidade de Coimbra · PTInserm · FRJohns Hopkins University · USKing Saud Medical City · SAMayo Clinic in Florida · USMedical University of Vienna · ATNewark Beth Israel Medical Center · USPhoenix Children's Hospital · USSaarland University · DEUniversitätskinderklinik · DEUniversity Hospital Münster · DEUniversity Medical Center Freiburg · DEUniversity of Cologne · DEUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionVosoritide is the first precision medical therapy approved to increase growth velocity in children with achondroplasia. Sharing early prescribing experiences across different regions could provide a framework for developing practical guidance for the real-world use of vosoritide.

methodsTwo meetings were held to gather insight and early experience from experts in Europe, the Middle East, and the USA. The group comprised geneticists, pediatric endocrinologists, pediatricians, and orthopedic surgeons. Current practices and considerations for vosoritide were discussed, including administration practicalities, assessments, and how to manage expectations.

resultsA crucial step in the management of achondroplasia is to determine if adequate multidisciplinary support is in place. Training for families is essential, including practical information on administration of vosoritide, and how to recognize and manage injection-site reactions. Advocated techniques include establishing a routine, empowering patients by allowing them to choose injection sites, and managing pain. Patients may discontinue vosoritide if they cannot tolerate daily injections or are invited to participate in a clinical trial. Clinicians in Europe and the Middle East emphasized the importance of assessing adherence to daily injections, as non-adherence may impact response and reimbursement. Protocols for monitoring patients receiving vosoritide may be influenced by regional differences in reimbursement and healthcare systems. Core assessments may include pubertal staging, anthropometry, radiography to confirm open physes, the review of adverse events, and discussion of concomitant or new medications-but timing of these assessments may also differ regionally and vary across institutions. Patients and families should be informed that response to vosoritide can vary in both magnitude and timing. Keeping families informed regarding vosoritide clinical trial data is encouraged.

conclusionThe early real-world experience with vosoritide is generally positive. Sharing these insights is important to increase understanding of the practicalities of treatment with vosoritide in the clinical setting.

Indexed as

AchondroplasiaNatriuretic Peptide, C-TypeChildDelivery of Health CareHumansPain ManagementNatriuretic Peptide, C-TypevosoritideAchondroplasiaAssessmentsClinical practiceEarly experienceGuidanceManagementMonitoringPracticalitiesVosoritide

Identifiers

PMID37882884
PMCPMC10796712
OpenAlexW4387949268

What OpenQuestion holds

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Registered trials

None linked

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.