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European Journal of Cancer, ISSN 0959-8049, 01/2017, Volume 70, p. 1
Soft tissue sarcomas (STS) are rare and heterogeneous tumours. A correct definition of STS is imperative from the very beginning of disease management. to... 
Prognosis | Sarcoma | Survivor | Clinical trials | Soft tissue sarcoma | Histology | Radiation therapy | Disease control | Subgroups | Chemotherapy | Computed tomography | Surgery | Diagnostic systems | Tumors
Journal Article
European Journal of Surgical Oncology, ISSN 0748-7983, 01/2019, Volume 45, Issue 1, pp. 16 - 18
Rare cancers represent approximately one fourth of all cancers. Despite being a heterogeneous group of diseases, they share similar problems including lack of... 
ERN | Rare cancers | Spoke | JARC | Hub | Networking | SURGERY | ONCOLOGY
Journal Article
Lancet, The, ISSN 0140-6736, 2012, Volume 379, Issue 9829, pp. 1879 - 1886
Journal Article
The Lancet, ISSN 0140-6736, 2013, Volume 381, Issue 9863, pp. 295 - 302
Background Until now, only imatinib and sunitinib have proven clinical benefi t in patients with gastrointestinal stromal tumours (GIST), but almost all... 
Journal Article
American Society of Clinical Oncology educational book / ASCO. American Society of Clinical Oncology. Meeting, 2015, pp. e629 - e633
Adjuvant chemotherapy is not standard treatment in soft tissue sarcoma (STS). However, when the risk of relapse is high, it is an option for shared decision... 
Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Humans | Sarcoma - mortality | Treatment Outcome | Clinical Trials as Topic | Chemotherapy, Adjuvant | Sarcoma - drug therapy | Sarcoma - pathology
Journal Article
Cancer Cell, ISSN 1535-6108, 02/2013, Volume 23, Issue 2, pp. 249 - 262
Journal Article
The Lancet, ISSN 0140-6736, 2004, Volume 364, Issue 9440, pp. 1127 - 1134
Journal Article
Annals of Oncology, ISSN 0923-7534, 2014, Volume 25 Suppl 3, Issue suppl 3, pp. iii113 - 23
Journal Article