Léčba Ewingova sarkomu/primitivního neuroektodermálního tumoru dospělých
| Title in English | Therapy for Ewing´s Family of Tumours in adults |
|---|---|
| Authors | |
| Year of publication | 2012 |
| Type | Article in Periodical |
| Magazine / Source | Onkologie |
| MU Faculty or unit | |
| Citation | |
| Web | http://www.onkologiecs.cz/pdfs/xon/2012/02/11.pdf |
| Field | Oncology and hematology |
| Keywords | Ewing s family of Tumours; multimodal therapy; toxicity; survival |
| Description | Ewing's Family of Tumours is most frequently observed in children and adolescent age. 90 % of patiens are younger than 20 years. Prognosis is unfavourable, with 5-year overall survival from 55 to 70 % in localized, not exceeding 20 % in primarily metastatic disease. The results of the therapy are getting worse by increasing age. Multidisciplinary treatment planning is mandatory in all cases of this tumor. We introduce our experience with EURO E.W.I.N.G. 99/EWING 2008 protocol in adult patients. |