Evidence map›Paper›PMID 42151365›Full record

ArticleCommunications medicine2026

Trametinib for multiple non-ossifying fibromas due to KRAS mosaic mutations: two case reports.

Marie Vincent, Soizic Tiriau, Marine Fouillet-Desjonqueres, Alicia Besson, Wassim Ouchetto, Sébastien Barbarot, Bertrand Isidor, Aymeric Rouchaud, Geneviève Baujat, Pierre Vabres and 3 more

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In one paragraph

Article in Communications medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Marie VincentService de Génétique Médicale, CHU Nantes, Nantes, France. marie.vincent@chu-nantes.fr.ORCID http://orcid.org/0000-0003-1010-5618
Soizic TiriauService de Pédiatrie-Spécialités, CHU Nantes, Nantes, France.
Marine Fouillet-DesjonqueresService de Néphrologie-Rhumatologie-Dermatologie Pédiatriques, Hospices Civils de, Lyon, France.
Alicia BessonUniversité Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.
Wassim OuchettoUniversité Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.
Sébastien BarbarotService de Dermatologie, CHU Nantes, Nantes, France.
Bertrand IsidorService de Génétique Médicale, CHU Nantes, Nantes, France.
Aymeric RouchaudService d'Imagerie Médicale, Hospices Civils de, Lyon, France.
Geneviève BaujatService de Génétique Médicale, Centre de Référence des Maladies Osseuses Constitutionnelles, Hôpital Necker-Enfants Malades, APHP, Paris, France.
Pierre VabresService de Dermatologie, CHU Dijon Bourgogne, Dijon, France.
Patrick EderyUniversité Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.
Marion DelousUniversité Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.
Massimiliano RossiCentre de référence des Maladies Osseuses Constitutionnelles, Hospices Civils de, Lyon, France.ORCID http://orcid.org/0000-0002-5797-8152

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKRAS mosaic activating variants are the main cause of non-ossifying fibromas (NOFs), the most common benign lesion of the growing skeleton. Multifocal NOFs cause bone fragility, and no specific treatment is currently available.

methodsWe report two children, carrying mosaic KRAS variants (p.G13D and p.A146T), presenting with oculoectodermal syndrome and recurrent fractures due to progressive polyostotic NOFs. To assess the impact of these mutations on KRAS function, we conducted transient KRAS overexpression in HEK293 cells and then tested the effect of the MEK-inhibitor trametinib at the cellular level.

resultsWe show that trametinib yields, in vitro, significant reduction of RAS-pathway hyperactivation induced by the two KRAS variants and, in vivo, remarkable clinical and radiological improvement with no recurrence of fractures and reossification of NOFs under treatment; resurgence of lesions is observed one year after stopping treatment.

conclusionsHence, trametinib constitutes a promising precision therapeutic approach for severe KRAS-related NOFs.

Identifiers

PMID42151365
PMCPMC13448663

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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.