Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Milea J. M. Timbergen"'
Autor:
Anne‐Rose W. Schut, Leanne E. deBruin, Belle H. deRooij, Emma Lidington, Milea J. M. Timbergen, Winette T. A. van derGraaf, Winan J. vanHoudt, Johannes J. Bonenkamp, Robin L. Jones, Dirk. J. Grünhagen, Stefan Sleijfer, Spyridon Gennatas, Cornelis Verhoef, Olga Husson
Publikováno v:
Cancer Medicine, Vol 12, Iss 12, Pp 13661-13674 (2023)
Abstract Background Desmoid‐type fibromatosis (DTF) has a highly variable clinical course with varying intensity of symptoms. The objectives of this study were to identify subgroups of DTF patients based on physical symptom burden and to compare sy
Externí odkaz:
https://doaj.org/article/68c9dc77427e4ed09f0bee452795e1f3
Autor:
Anne-Rose W. Schut, Emma Lidington, Milea J. M. Timbergen, Eugenie Younger, Winette T. A. van der Graaf, Winan J. van Houdt, Johannes J. Bonenkamp, Robin L. Jones, Dirk. J. Grünhagen, Stefan Sleijfer, Cornelis Verhoef, Spyridon Gennatas, Olga Husson
Publikováno v:
Cancers, Vol 14, Iss 12, p 2979 (2022)
Desmoid-type fibromatosis (DTF) is a rare, soft-tissue tumour. These tumours do not metastasize, but their local aggressive tumour growth and unpredictable behaviour can have a significant impact on health-related quality of life (HRQoL). Little is k
Externí odkaz:
https://doaj.org/article/19aac83196cf4092a8787fd073c92bcf
Autor:
Milea J. M. Timbergen, Ruben Boers, Anne L. M. Vriends, Joachim Boers, Wilfred F. J. van IJcken, Marla Lavrijsen, Dirk J. Grünhagen, Cornelis Verhoef, Stefan Sleijfer, Ron Smits, Joost Gribnau, Erik A. C. Wiemer
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
IntroductionThe majority of desmoid-type fibromatosis (DTF) tumors harbor a β-catenin mutation, affecting specific codons in CTNNB1 exon 3. S45F tumors are reported to have a higher chance of recurrence after surgery and more resistance to systemic
Externí odkaz:
https://doaj.org/article/5a25b29956a948f185e222b601fec78d
Autor:
Milea J. M. Timbergen, Winette T. A. van der Graaf, Dirk J. Grünhagen, Eugenie Younger, Stefan Sleijfer, Alison Dunlop, Lucy Dean, Cornelis Verhoef, Lonneke V. van de Poll-Franse, Olga Husson
Publikováno v:
Sarcoma, Vol 2020 (2020)
Purpose. Desmoid-type fibromatosis (DTF) is a rare, nonmetastasising soft tissue tumour. Symptoms, unpredictable growth, lack of definitive treatments, and the chronic character of the disease can significantly impact health-related quality of life (
Externí odkaz:
https://doaj.org/article/5e118e83dd7e48eebe5f0f06dbf40002
Autor:
Anne-Rose W. Schut, Emma Lidington, Milea J. M. Timbergen, Eugenie Younger, Winette T. A. van der Graaf, Winan J. van Houdt, Johannes J. Bonenkamp, Robin L. Jones, Dirk. J. Grünhagen, Stefan Sleijfer, Cornelis Verhoef, Spyridon Gennatas, Olga Husson
Publikováno v:
Cancers, Vol 14, Iss 3, p 709 (2022)
Sporadic desmoid-type fibromatosis (DTF) is a rare, non-metastasising soft-tissue tumour. Patients can experience a variety of disease-specific issues related to the unpredictable clinical course and aggressiveness of DTF, which negatively impacts he
Externí odkaz:
https://doaj.org/article/1430580bf80149bda0224d5f28cb0ed2
Autor:
Anne-Rose W. Schut, Milea J. M. Timbergen, Emma Lidington, Dirk J. Grünhagen, Winette T. A. van der Graaf, Stefan Sleijfer, Winan J. van Houdt, Johannes J. Bonenkamp, Eugenie Younger, Alison Dunlop, Robin L. Jones, Cornelis Verhoef, Spyridon Gennatas, Olga Husson
Publikováno v:
Cancers, Vol 13, Iss 13, p 3068 (2021)
Sporadic desmoid-type fibromatosis (DTF) is a rare soft tissue tumour with an unpredictable clinical course. These tumours are incapable of metastasising, but their local aggressive tumour growth and tendency to recur locally can result in a substant
Externí odkaz:
https://doaj.org/article/7b0985914ed74d8ebf99d1d7e39b70ec
Autor:
Milea J. M. Timbergen, Ron Smits, Dirk J. Grünhagen, Cornelis Verhoef, Stefan Sleijfer, Erik A. C. Wiemer
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
Desmoid-type fibromatosis (DTF) is a rare, soft tissue tumor of mesenchymal origin which is characterized by local infiltrative growth behavior. Besides “wait and see,” surgery and radiotherapy, several systemic treatments are available for sympt
Externí odkaz:
https://doaj.org/article/52eba05871684ed1b8392c3271f37423
Autor:
Anne-Rose W. Schut, Milea J. M. Timbergen, Danique L. M. van Broekhoven, Thijs van Dalen, Winan J. van Houdt, Johannes J. Bonenkamp, Stefan Sleijfer, Dirk J. Grunhagen, Cornelis Verhoef
Publikováno v:
Annals of Surgery, 277, 4, pp. 689-696
Annals of Surgery, 277(4), 689-696. Lippincott Williams & Wilkins
Annals of Surgery, 277, 689-696
Annals of Surgery, 277(4), 689-696. Lippincott Williams & Wilkins
Annals of Surgery, 277, 689-696
Contains fulltext : 291068.pdf (Publisher’s version ) (Open Access) OBJECTIVE: To assess tumor behavior and the efficacy of active surveillance (AS) in patients with desmoid-type fibromatosis (DTF). SUMMARY OF BACKGROUND DATA: AS is recommended as
Autor:
Erik A.C. Wiemer, Sébastien Salas, Hee Sung Kim, Cornelis Verhoef, Joost van Rosmalen, Chiara Colombo, Yoshihiro Nishida, Michel Renckens, Dirk J. Grünhagen, Alessandro Gronchi, Milea J. M. Timbergen, Stefan Sleijfer, P. Colombo, John T. Mullen
Publikováno v:
Annals of Surgery, 273(6), 1094-1101. Lippincott Williams & Wilkins
OBJECTIVE: This meta-analysis (PROSPERO CRD42018100653) uses individual patient data (IPD) to assess the association between recurrence and CTNNB1 mutation status in surgically treated adult desmoid-type fibromatosis (DTF) patients.SUMMARY OF BACKGRO
Autor:
Milea J. M. Timbergen, Dirk J. Grünhagen, Cornelis Verhoef, Stefan Sleijfer, Anne-Rose W. Schut
Publikováno v:
European Journal of Cancer, 137, 18-29. Elsevier Ltd.
BACKGROUND: This study evaluates the results of the active surveillance (AS) approach in adult patients with desmoid-type fibromatosis (DTF) because AS is advocated as a front-line approach for DTF in the European consensus guidelines.METHODS: A syst