Communications medicine · 2026
Trametinib for multiple non-ossifying fibromas due to KRAS mosaic mutations: two case reports.
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Vincent Marie, Tiriau Soizic, Fouillet-Desjonqueres Marine, Besson Alicia, Ouchetto Wassim, Barbarot Sébastien, Isidor Bertrand, Rouchaud Aymeric, Baujat Geneviève, Vabres Pierre, Edery Patrick, Delous Marion, Rossi Massimiliano
Аннотация
BACKGROUND: KRAS 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.
METHODS: We 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.
RESULTS: We 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.
CONCLUSIONS: Hence, trametinib constitutes a promising precision therapeutic approach for severe KRAS-related NOFs.
METHODS: We 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.
RESULTS: We 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.
CONCLUSIONS: Hence, trametinib constitutes a promising precision therapeutic approach for severe KRAS-related NOFs.