BACKGROUND. The treatment of Ewing's sarcoma consists of chemotherapy
for systemic and local disease. However, the role of radiation therapy
, and/or surgical resection for definitive local treatment has yet to
be determined. METHODS. A retrospective review of 32 patients (24 male
s and 8 females) treated for femoral Ewing's sarcoma between 1970 and
1985 was performed. Patients were divided into 3 treatment groups: che
motherapy and radiotherapy (CR) (10); chemotherapy and surgery (CS) (9
); and chemotherapy, surgery, and radiotherapy (CSR) (13). Patients in
the CR group received a mean of 5320 centigray (cGy) of radiation and
patients in the CSR group received a mean of 3590 cGy. Multiagent cyc
lophosphamide/doxorubicin based chemotherapy was used in all cases. Su
rgery consisted of wide resection or amputation. RESULTS. Patients in
the CR group had a higher risk of local recurrence than patients in th
e CS and CSR groups (P = 0.02, log rank). The combination of local rec
urrences and treatment complications necessitated surgery for 7 of 10
CR patients, whereas 1 of 9 and 4 of 13 in the CS and CSR groups requi
red additional surgery. The median survival for the entire group was 3
9 months, Minimum followup for surviving patients was 45 months. Five-
year survival consisted of 1 of 10 patients in the CR group, 2 of 9 in
the CS group, and 7 of 13 in the CSR group. There were no statistical
ly significant differences among the three survival curves. Tumor loca
tion within the femur was a significant prognostic variable. Distal fe
moral location had a survival advantage compared with proximal and mid
-femur locations (P = 0.049, log rank). CONCLUSIONS. Femoral Ewing's s
arcoma remains a disease with a poor prognosis. Radiation alone for lo
cal treatment results in a high rate of local recurrence and complicat
ions. Our current local treatment strategy for femoral Ewing's sarcoma
includes surgery in all and adjuvant radiotherapy in many of the pati
ents. (C) 1996 American Cancer Society.