TY  - GEN
AU  - Kasper, B.
AU  - Baumgarten, C.
AU  - Garcia, J.
AU  - Bonvalot, S.
AU  - Haas, R.
AU  - Haller, F.
AU  - Hohenberger, P.
AU  - Penel, N.
AU  - Messiou, C.
AU  - van der Graaf, W. T.
AU  - Gronchi, A.
AU  - Desmoid Working Grp
PY  - 2017
DO  - 10.1093/annonc/mdx323
SN  - 0923-7534
UR  - https://hdl.handle.net/10668/27274
T2  - Annals of oncology
AB  - Desmoid-type fibromatosis is a rare and locally aggressive monoclonal, fibroblastic proliferation characterized by a variable and often unpredictable clinical course. Currently, there is no established or evidence-based treatment approach available...
LA  - en
PB  - Oxford univ press
KW  - desmoid
KW  - aggressive fibromatosis
KW  - EORTC/STBSG
KW  - patient advocacy groups
KW  - SPAEN
KW  - treatment algorithm
KW  - Advanced aggressive fibromatosis
KW  - Phase-ii trial
KW  - Soft-tissue
KW  - Local recurrence
KW  - Abdominal-wall
KW  - 1st-line management
KW  - Surgical resection
KW  - Prognostic-factors
KW  - Treatment options
KW  - See policy
TI  - An update on the management of sporadic desmoid-type fibromatosis: a European Consensus Initiative between Sarcoma PAtients EuroNet (SPAEN) and European Organization for Research and Treatment of Cancer (EORTC)/Soft Tissue and Bone Sarcoma Group (STBSG)
TY  - review
VL  - 28
ER  -