Skip to content
← Ewing Sarcoma and Undifferentiated Small Round Cell Sarcomas of Bone and Soft Tissue

FOR PATIENTS · SOURCE READING

Chemotherapy

Source: Ewing Sarcoma Treatment (PDQ®)–Patient Version, National Cancer Institute.

Source updated: February 28, 2025 · Captured 2026-09-09.

Selected source text with whitespace normalised. This Triangle page is not an NCI PDQ summary. Independent clinical review is pending.

Context: Treatment Option Overview / The following types of treatment are used:

Chemotherapy (also called chemo) uses drugs to stop the growth of cancer cells. Chemotherapy either kills the cancer cells or stops them from dividing.

Chemotherapy for Ewing sarcoma is taken by mouth or injected into a vein. When given this way, the drugs enter the bloodstream and can reach cancer cells throughout the body. Systemic combination chemotherapy is often given to shrink the tumor before surgery or radiation therapy and to kill any cancer cells that have spread to other parts of the body. It is often the first treatment given and lasts for about 6 to 12 months.

Source links and citations

Chemotherapy drugs used alone or in combination to treat Ewing sarcoma include:

cyclophosphamide

Source links and citations

docetaxel

Source links and citations

doxorubicin

Source links and citations

etoposide

Source links and citations

gemcitabine

Source links and citations

ifosfamide

Source links and citations

irinotecan

Source links and citations

temozolomide

Source links and citations

topotecan

Source links and citations

vincristine

Source links and citations

Other chemotherapy drugs not listed here may also be used.

Learn more about how chemotherapy works, how it is given, common side effects, and more at Chemotherapy to Treat Cancer.

Source links and citations

Preserved source evidence · Independent clinical review pending · Not medical advice