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Pazopanib is an active treatment in desmoid tumour/aggressive fibromatosis

BACKGROUND: Desmoid tumours/aggressive fibromatosis (DT/AF) are infrequent soft-tissue neoplasms. They usually behave as indolent diseases. However, they may grow locally infiltrating or compressing adjacent structures. The role of local treatment is limited and only a few drugs have shown activity....

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Detalles Bibliográficos
Autores principales: Martin-Liberal, Juan, Benson, Charlotte, McCarty, Heather, Thway, Khin, Messiou, Christina, Judson, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176486/
https://www.ncbi.nlm.nih.gov/pubmed/24279994
http://dx.doi.org/10.1186/2045-3329-3-13
Descripción
Sumario:BACKGROUND: Desmoid tumours/aggressive fibromatosis (DT/AF) are infrequent soft-tissue neoplasms. They usually behave as indolent diseases. However, they may grow locally infiltrating or compressing adjacent structures. The role of local treatment is limited and only a few drugs have shown activity. CASES PRESENTATION: We report the outcome of two patients affected by progressive DT/AF treated with the angiogenesis inhibitor pazopanib in two different institutions. Both patients achieved dramatic improvement in their symptoms and radiological signs of response. The clinical benefit lasted for more than 1 year and it is still ongoing. CONCLUSIONS: Pazopanib is an active treatment in DT/AF. It is the first time this has been reported.