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Desmoid Tumors-Experience from a Referral Center, Part 1: Multidisciplinary Review and Practical Recommendations
Alvarez Alvarez Rosa1, Agra Pujol Carolina2, Arregui Valles Marta1
1Medical Oncology Department, Instituto de Investigacion Sanitaria Gregorio Marañon, Hospital General Universitario Gregorio Marañon, 28007 Madrid, Spain.
None:
Desmoid tumors (DTs), also known as aggressive fibromatosis, are rare neoplasms characterized by local invasiveness and a high risk of recurrence, despite their lack of metastatic potential. The management of these tumors remains challenging due to their unpredictable behavior and heterogeneous presentations. In this two-part study, we first provide a comprehensive review of the scientific evidence on diagnosis and emerging therapeutic strategies for DT. In the second part, we will present a retrospective analysis of our experience at a national reference center for sarcoma treatment, focusing on diagnostic strategies, therapeutic interventions, and clinical outcomes.
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