BACKGROUND. Data regarding the value of cytoreduction and cell histolo
gy in ovarian sarcomas are limited. The goal of this study was to asse
ss the value of surgical cytoreduction, preoperative CA 125 levels, st
age, histology, and platinum-based chemotherapy in the primary treatme
nt of ovarian sarcomas. METHODS. A retrospective analysis of 47 women
with primary ovarian sarcomas was performed. RESULTS. Forty-one patien
ts (87%) presented with advanced stage disease (International Federati
on of Gynecology and Obstetrics Stage III or IV. Optimal surgical cyto
reduction (<1 cm residual tumor burden) was achieved in 25 patients (5
3%). Forty patients (85%) had a malignant mixed mullerian tumor wherea
s 7 patients had a pure sarcoma. Eighteen women with mixed mullerian t
umors had homologous tumors and 22 had heterologous elements. Patients
treated with platinum-based chemotherapy were significantly more like
ly to have a response (P = 0.008) compared with those treated with oth
er regimens. Treatment with platinum-based chemotherapy also showed a
survival advantage (P = 0.03). Preoperative CA 125 levels were elevate
d (>35 U/mL) in 93% of patients with ovarian sarcomas. A preoperative
CA 125 level < 75 U/mL was significantly associated with better surviv
al (P = 0.01). In univariate analysis, other significant predictors of
improved survival were early stage (P = 0.04), homologous tumors (P <
0.05), and optimal surgical cytoreduction (P < 0.001). In multivariat
e analysis of various prognostic variables, optimal surgical cytoreduc
tion (P < 0.001) was the most significant factor, followed by histolog
ic subtype (P < 0.02). CONCLUSIONS, Ovarian sarcomas are rare malignan
cies with a poor prognosis, All women with suspected ovarian carcinoma
or sarcoma should have a preoperative CA 125 level taken. Surgical cy
toreduction to a residual tumor burden of cl cm improves outcome and s
hould be the goal of surgery. Although the optimal consolidation chemo
therapy regimen remains unknown, platinum should be included as part o
f the regimen. (C) 1998 Americnn Cancer Society.