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- Publications
- Influence
Variability in Patterns of Recurrence After Resection of Primary Retroperitoneal Sarcoma (RPS): A Report on 1007 Patients From the Multi-institutional Collaborative RPS Working Group
- A. Gronchi, D. Strauss, +17 authors C. Raut
- Medicine
- Annals of surgery
- 1 May 2016
Background:Retroperitoneal sarcomas (RPS) are rare tumors composed of several well defined histologic subtypes. The aim of this study was to analyze patterns of recurrence and treatment variations in… Expand
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…
- B. Kasper, C. Baumgarten, +30 authors M. Wartenberg
- Medicine
- Annals of oncology : official journal of the…
- 23 June 2017
Abstract 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… Expand
Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.
- J. Blay, A. Bertuzzi, +38 authors P. Casali
- Medicine
- Annals of oncology : official journal of the…
- 1 September 2015
Primary bone tumors are rare, accounting for <0.2% of malignant tumors registered in the EUROCARE database [1]. Different tumors have distinct patterns of incidence. Osteosarcoma and Ewing sarcoma… Expand
Management of sporadic desmoid-type fibromatosis: a European consensus approach based on patients' and professionals' expertise - a sarcoma patients EuroNet and European Organisation for Research and…
- B. Kasper, C. Baumgarten, +6 authors A. Gronchi
- Medicine
- European journal of cancer
- 2015
Desmoid-type fibromatosis (DF) is a rare monoclonal, fibroblastic proliferation characterised by a variable and often unpredictable clinical course. It may affect nearly all parts of the body… Expand
Soft tissue and visceral sarcomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up.
- P. Casali, N. Abecassis, +60 authors J. Blay
- Medicine
- Annals of oncology : official journal of the…
- 1 October 2018
Fondazione IRCCS Istituto Nazionale dei Tumori and University of Milan, Milan, Italy; Instituto Portugues de Oncologia de Lisboa Francisco Gentil, EPE, Lisbon, Portugal; University Hospital Essen,… Expand
Gastrointestinal stromal tumours: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up.
- P. Casali, N. Abecassis, +60 authors J. Blay
- Medicine
- Annals of oncology : official journal of the…
- 1 October 2018
Fondazione IRCCS Istituto Nazionale dei Tumori and University of Milan, Milan, Italy; Instituto Portugues de Oncologia de Lisboa Francisco Gentil, EPE, Lisbon, Portugal; University Hospital Essen,… Expand
Bone sarcomas: ESMO-PaedCan-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up.
- P. Casali, S. Bielack, +70 authors J. Blay
- Medicine
- Annals of oncology : official journal of the…
- 1 October 2018
Primary bone tumours are rare, accounting for < 0.2% of malignant neoplasms registered in the EUROCARE (European Cancer Registry based study on survival and care of cancer patients) database.… Expand
Does the combination of radiotherapy and debulking surgery favor survival in paranasal sinus carcinoma?
- E. Jansen, R. Keus, F. Hilgers, R. Haas, I. B. Tan, H. Bartelink
- Medicine
- International journal of radiation oncology…
- 2000
PURPOSE
To determine the contribution of debulking surgery on local control and survival in paranasal sinus tumors. As most patients present with locally advanced disease, the possibility of radical… Expand
Evaluation of response after neoadjuvant treatment in soft tissue sarcomas; the European Organization for Research and Treatment of Cancer-Soft Tissue and Bone Sarcoma Group (EORTC-STBSG)…
- E. Wardelmann, R. Haas, +13 authors S. Bonvalot
- Medicine
- European journal of cancer
- 2016
At present, there is not a commonly used and generally accepted standardized approach for the pathologic evaluation of pretreated soft tissue sarcomas. Also, it is still unclear whether the cut-off… Expand
A phase I study on the combination of neoadjuvant radiotherapy plus pazopanib in patients with locally advanced soft tissue sarcoma of the extremities
- R. Haas, H. Gelderblom, +12 authors F. van Coevorden
- Medicine
- Acta oncologica
- 26 August 2015
Abstract Accumulating evidence suggests significant synergism combining radiotherapy (RT) with angiogenesis targeted therapies. This multicenter prospective phase I clinical trial established the… Expand
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