Background: Uterine sarcomas are rare, charaterized by rapid clinical
progression and poor prognosis, and their management has been a challe
nge. The purpose of this study was to investigate the clinical and his
tologic findings, treatment, and outcome of patients with uterine sarc
oma in the south of Israel. Methods: Data from the files of 36 patient
s with uterine sarcoma who were managed at the Soroka Medical Center b
etween January 1961 and December 1994 were evaluated. Results: The 5-y
ear survival rate was 32% overall; 63% for 9 patients with endometrial
stromal sarcoma (ESS), 30% for 14 patients with mixed mesodermal sarc
oma (MMS) and 18% for 13 patients with leiomyosarcoma (LMS); 41% for 2
2 patients with Stage I and 19% for 14 patients with Stages II, III, a
nd IV. Only the difference in the 5-year survival rate between ESS and
LMS was statistically significant (P < 0.05). Eleven patients (30.6%)
were treated with surgery alone, 4 (11.1%) with surgery followed by p
elvic radiotherapy, 11 (30.6%) with surgery followed by chemotherapy,
8 (22.2%) with surgery followed by pelvic radiotherapy and chemotherap
y, one (2.8%) with chemotherapy alone, and one (2.8%) had no treatment
. Conclusions: Uterine sarcomas are aggressive tumors with a poor prog
nosis. The treatment is surgery generally followed by adjuvant pelvic
radiotherapy and/or systemic chemotherapy. (C) 1997 Wiley-Liss, Inc.