EVALUATION OF THE PROGNOSTIC VALUE OF MORPHOMETRIC FEATURES AND CELLULAR DNA CONTENT IN FIGO-I OVARIAN-CANCER PATIENTS

  • 1 August 1987
    • journal article
    • research article
    • Vol. 9  (4) , 287-290
Abstract
Approximately 20% to 40% of the patients with a FIGO I ovarian tumor die within five years after the diagnosis. Morphologic studies (typing and grading) of the primary tumor are prognostically important, but poorly reproducible. Therefore, the prognostic value of more objective techniques, such as morphometry and flow cytometric (FCM) DNA determinations, were evaluated in 33 adequately staged FIGO I patients with at least a five-year follow-up. The overall five-year survival in the group was 64%. Three patient categories were defined on the basis of two easily measured morphometric features, the mitotic activity index (MAI) and the volume percentage epithelium (VPE), which an earlier study had proved to be significantly associated with prognosis. The five-year survival rates were 91% for 11 patients in category A (MAI < 30 and VPE < 65), 67% for 9 patients in category B (MAI < 30 and VPE .gtoreq. 65) and 38% for 13 patients in category C (MAI .gtoreq. 30). FCM showed 25 of the tumors to be diploid and 8 to be aneuploid. The cellular DNA content was also of prognostic value: the five-year survival figures for patients with diploid and aneuploid tumors were 68% and 37%, respectively. Combination of the morphometric and FCM features showed that, in diploid tumors, the morphometric features have additional prognostic value: the diploid-tumor-patient survival rates in categories A, B and C were 91%, 63% and 50%, respectively. None of the eight patients with aneuploid tumors fell in the morphometrically favorable category A while seven were in category C. The five-year survival rate of the latter patients was only 29%. These results show that, in patients with a FIGO I ovarian tumor of the common epithelial type, easily assessed morphometric features contain most of the prognostic information. The additional assessment of cellular DNA content is of some value for discerning a subset of especially aggressive aneuploid tumors, which also have morphometric characteristics associated with an unfavorable outcome.

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