G. Olt et al., PREOPERATIVE EVALUATION OF MACROPHAGE-COLONY-STIMULATING FACTOR LEVELS IN PATIENTS WITH ENDOMETRIAL CANCER, American journal of obstetrics and gynecology, 174(4), 1996, pp. 1316-1319
OBJECTIVE: Our purpose was to examine the relationship between preoper
ative serum levels of macrophage colony-stimulating factor, alone and
in combination with CA 125, and the presence of prognostic clinicopath
ologic factors and subclinical metastases in women with endometrial ca
ncer. STUDY DESIGN: Ninety-two women who underwent primary exploration
for endometrial adenocarcinoma had preoperative serum samples evaluat
ed for macrophage colony-stimulating factor and CA 125 levels. Multiva
riate analysis was used to determine the associations of surgicopathol
ogic findings with macrophage colony-stimulating factor and CA 125 lev
els. Logistic regression analysis was used to identify factors associa
ted with the risk of extrauterine disease. The association of macropha
ge colony-stimulating factor and CA 125 levels with stage, grade, and
depth of myometrial invasion and histologic characteristics were analy
zed with Fisher's two-tailed exact test. RESULTS: Elevated levels of m
acrophage colony-stimulating factor were not associated with depth of
myometrial invasion, histologic grade, or histologic cell type; howeve
r, advanced stage (p = 0.02) and the presence of lymph node metastases
(p = 0.04) were associated with elevated levels. Sensitivity and spec
ificity of macrophage colony-stimulating factor for predicting extraut
erine disease were 42% and 89%, respectively if either an elevated mac
rophage colony-stimulating factor or an elevated CA 125 level was used
to predict extrauterine disease, the sensitivity was increased to 67%
but the specificity was decreased to 78%. Macrophage colony-stimulati
ng factor elevations predicted lymph node metastases with a sensitivit
y of 50% and a specificity of 86%. A multivariate regression model sho
wed CA 125 to be the most significant predictor of extrauterine diseas
e; macrophage colony-stimulating factor also contributed prognostic in
formation (p = 0.02). The sensitivity and specificity of the multivari
ate model for predicting extrauterine disease were 75% and 73%, respec
tively. CONCLUSION: Macrophage colony-stimulating factor and CA 125 ar
e neither sensitive nor specific enough to be used as predictors of th
e presence or absence of extrauterine disease in patients with endomet
rial cancer.