Purpose: The improved survival in patients with Ewing's sarcoma over t
he past two decades has placed increased importance on achievement of
local disease control, Ewing's sarcoma that arises in the pelvis has b
een recognized to have a worse prognosis than that in the appendicular
skeleton, and the role of surgical resection in these cases remains c
ontroversial. The current study attempts to identify a benefit to surg
ical resection in these patients. Methods: We retrospectively examined
39 patients who presented with Ewing's sarcoma in a pelvic location,
all of whom were treated systemically with chemotherapy, Twenty patien
ts received radiation only as a means of local control, and 19 underwe
nt resection with or without radiation therapy, The patients were eval
uated with end points of disease-free survival and overall survival fo
r a minimum of 24 months and a mean of 58 months. Results: There was a
n even distribution among patients who underwent surgical resection fo
r local control as compared with those who received only radiation the
rapy with respect to age, site, date of treatment, and stage of diseas
e, Despite uncontrolled biases including tumor size and response to ch
emotherapy that would be expected to favor patients who undergo resect
ion, surgery in addition to or in substitution for radiation therapy d
id not result in a statistically significant increase in disease-free
survival or overall survival. Local disease control was comparable bet
ween those who underwent resection and those who did not: three patien
ts in each group developed a local recurrence. Conclusion: Currently,
morbidity of surgical resection should be weighed against the efficacy
and secondary complications of radiation therapy in the decision-maki
ng process for local disease control, The issue of whether overall sur
vival and local disease control is improved in patients who undergo su
rgical resection remains controversial and may require a prospective r
andomized trial to be answered definitively. (C) 1995 by American Soci
ety of Clinical Oncology.