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Primary Mediastinal Ewing's Sarcoma: Post Hoc Analysis from Two International Multicenter Prospective Randomized
Theresa Stork1,2,3, Andreas Ranft3,4, Clemens Aigner1,3,5
1Department of Thoracic Surgery, Ruhrlandklinik, University of Duisburg-Essen, 45239 Essen, Germany.
Primary mediastinal Ewing sarcoma (EWS) is a rare cancer, accounting for 0.3% of all EWS cases. This study found a 64% five-year survival rate, with surgery improving outcomes for non-metastatic patients.
Area of Science:
- Oncology
- Pediatric Oncology
- Sarcoma Research
Background:
- Primary mediastinal Ewing sarcoma (EWS) is an exceptionally rare malignancy.
- Few cases have been documented in existing medical literature.
- Understanding this rare EWS subtype is crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the characteristics of primary mediastinal EWS.
- To analyze patient and treatment data from two international EWS trials.
- To determine the survival rates and treatment efficacy for this rare cancer.
Main Methods:
- Retrieved data from the EURO-E.W.I.N.G.99 and EWING 2008 clinical trials.
- Analyzed patient demographics, diagnostic information, and treatment modalities.
- Evaluated survival outcomes based on treatment interventions.
Main Results:
- Primary mediastinal EWS represented 0.3% of all EWS cases (9 out of 2969 patients).
- The median age at diagnosis was 30.5 years, with 33% presenting with metastases.
- Five-year survival was 64%; patients undergoing surgery showed favorable survival, with all survivors having had surgery.
Conclusions:
- Primary mediastinal EWS is exceedingly rare, comprising only 0.3% of EWS cases.
- The five-year survival rate is comparable to EWS of other origins and favorable compared to other mediastinal sarcomas.
- Surgical intervention appears to be associated with improved survival in non-metastatic primary mediastinal EWS.
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