M. Brinkhuis et al., QUANTITATIVE PATHOLOGICAL VARIABLES AS PROGNOSTIC FACTORS FOR OVERALLSURVIVAL IN DANISH PATIENTS WITH FIGO STAGE-III OVARIAN-CANCER, International journal of gynecological cancer, 6(3), 1996, pp. 168-174
Earlier studies have shown the strong prognostic value of the mitotic
activity index (MAI), volume percent of epithelium (VPE), mean nuclear
area (MNA) and the standard deviation of the nuclear area (SDNA) in e
arly and advanced ovarian cancer. In one study of Danish patients howe
ver, these features were not significant and methodological causes wer
e excluded as a cause of this. Therefore, we have re-evaluated these f
eatures in another group of 112 Danish patients with FIGO stage III ov
arian cancer who were treated with debulking surgery followed by cispl
atin combination chemotherapy. Thirty-seven patients (33%) survived. I
n survival analysis residual disease status, performance status, perit
oneal carcinomatosis, histologic grade, age and the presence or absenc
e of ascites had significant influence on the eventual clinical outcom
e. Of the quantitative pathologic features the MAI, MNA, SDNA were cor
related with grade, but had stronger prognostic value than grade. Resi
dual disease status, performance status at diagnosis, peritoneal carci
nomatosis, the MNA and the SDNA were the best single prognostic variab
les (P < 0.00001). With multivariate analysis residual disease status,
MNA and age had independent additional value (grade was not selected
once these more significant features were included). With this combina
tion (called F3MS) four prognostically important groups could be disti
nguished (MC = 61.7, P < 0.00001). Survival in the most favourable F3M
S group (n = 28) was 71% (median survival time 84 months), while in th
e worst group (n = 29) none of the patients survived and the median su
rvival time in this group was only 13 months (Relative Risks (RR) = 3.
50). It is concluded that morphometric variables have important value
in predicting prognosis in patients with FIGO stage III ovarian cancer
and add to the classical prognostic factors of residual disease statu
s and age.