HEALTH PROFESSIONAL · SOURCE READING
Treatment of Metastatic Ewing Sarcoma
Source: Ewing Sarcoma and Undifferentiated Small Round Cell Sarcomas of Bone and Soft Tissue Treatment (PDQ®)–Health Professional Version, National Cancer Institute.
Source updated: November 27, 2024 · Captured 2026-09-09.
Selected source text with whitespace normalised. This Triangle page is not an NCI PDQ summary.
Approximately 25% of patients with Ewing sarcoma have metastases at diagnosis.[1] The prognosis is poor for patients with metastatic disease. With current therapies, patients who present with metastatic disease have a 6-year event-free survival (EFS) rate of approximately 28% and an overall survival (OS) rate of approximately 30%.[2,3] For patients with lung/pleural metastases only, the 6-year EFS rate is approximately 40% when using bilateral lung irradiation.[2,4] In contrast, patients with bone/bone marrow metastases have a 4-year EFS rate of approximately 28%, and patients with combined lung and bone/bone marrow metastases have a 4-year EFS rate of approximately 14%.[4,5]
The following factors independently predict a poor outcome in patients presenting with metastatic disease:[3]
Source links and citations
Age older than 14 years.
Primary tumor volume of more than 200 mL.
More than one bone metastatic site.
Bone marrow metastases.
Additional lung metastases.
Pulmonary metastases lack of complete response to induction chemotherapy.[6]
Source links and citations
Standard treatment options for metastatic Ewing sarcoma include the following:
Chemotherapy.
Source links and citations
Surgery.
Source links and citations
Radiation therapy.
Source links and citations
Continue within this section
Publication references
Read the original reference and check its publication notices.
Preserved source evidence · Not medical advice
Triangle