Abstract
OBJECTIVE:: To review an institutional experience with radiotherapy (RT) in patients with metastatic Ewing sarcoma. METHODS:: Thirty patients with metastatic Ewing sarcoma were considered. Twenty-nine received multiagent chemotherapy, whereas 22 had local therapy, which included RT in 14, surgery in 5, and surgery followed by RT in 3. RESULTS:: The 5-year overall survival rate was 22.1%. On multivariate analysis, presence of uncommon sites of metastasis (brain, liver, spleen) (P<0.0001) and use of local therapy to the primary site (P<0.001) were adverse factors for survival. Local control was not achieved in the 8 patients receiving only chemotherapy. All long-term survivors had local therapy including RT to metastatic bony sites and whole-lung irradiation for pulmonary metastasis. CONCLUSIONS:: The presence of uncommon sites of metastasis confers a worse prognosis. Aggressive primary treatment including RT to metastatic sites should be considered in these patients.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 283-286 |
| Number of pages | 4 |
| Journal | American Journal of Clinical Oncology: Cancer Clinical Trials |
| Volume | 36 |
| Issue number | 3 |
| DOIs | |
| State | Published - Jun 2013 |
Keywords
- Ewing sarcoma
- metastasis
- prognosis
- radiation therapy
ASJC Scopus subject areas
- Oncology
- Cancer Research
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