Preoperative evaluation of tumor ploidy in endometrial carcinoma - An accurate tool to identify patients at risk for extrauterine disease and recurrence
T. Susini et al., Preoperative evaluation of tumor ploidy in endometrial carcinoma - An accurate tool to identify patients at risk for extrauterine disease and recurrence, CANCER, 86(6), 1999, pp. 1005-1012
BACKGROUND. Tumor ploidy is a strong prognostic factor in patients with end
ometrial carcinoma, but generally is evaluated only after surgery. The avai
lability of a simple and reliable method to determine tumor ploidy before a
ny treatment is initiated could be helpful in the selection of patients at
high risk for advanced primary disease and subsequent recurrence, with seve
ral possible benefits. The objectives of the current study were: 1) to test
the accuracy of flow cycometric determination of tumor ploidy from preoper
ative outpatient endometrial biopsies compared with standard postoperative
evaluation from the surgical specimen and 2) to correlate this preoperative
parameter with the local recurrence and extrauterine tumor spread.
METHODS, Tumor ploidy from both preoperative biopsy material and the macros
copic surgical specimens was evaluated prospectively in 50 consecutive pati
ents with endometrial carcinoma. DNA analyses were performed in a blind fas
hion. Patients were followed for a median of 26 months (range, 16-46 months
).
RESULTS. In 9 of 50 cases (18%) an aneuploid tumor was found by the standar
d postoperative analysis. All 9 aneuploid tumors (100%) also were identifie
d correctly by the preoperative test on biopsy material. Occult extrauterin
e tumor spread was found in 10 patients (20%). The incidence rate of aneupl
oidy among these tumors was 50% compared with 10% in surgical International
Federation of Gynecology and Obstetrics Stage I tumors (P = 0.01). The rec
urrence rate was 55.5% (5 of 9 tumors) in the aneuploid group and 2.4% (1 o
f 41 tumors) in the diploid group (P < 0.001). The disease free survival ra
tes of patients with diploid and aneuploid tumors were 97.5% and 44.4%, res
pectively (P < 0.0001).
CONCLUSIONS. Preoperative tumor ploidy determination based on outpatient en
dometrial biopsy is as accurate as the standard postoperative evaluation in
patients with endometrial carcinoma. Tumor aneuploidy confirms the usefuln
ess of this method in selecting patients at risk for occult extrauterine tu
mor diffusion and recurrence. (C) 1999 American Cancer Society.