P. Rohlke et al., P53 IS A PERSISTENT AND PREDICTIVE MARKER IN ADVANCED OVARIAN CARCINOMAS - MULTIVARIATE-ANALYSIS INCLUDING COMPARISON WITH KI67 IMMUNOREACTIVITY, Journal of cancer research and clinical oncology, 123(9), 1997, pp. 496-501
p53 mutation and p53 protein overexpression are common findings in ova
rian carcinomas. In order to evaluate the prognostic significance of t
he p53 status and its role in metastasis, we examined 104 ovarian carc
inomas, among them 83 cases with follow-up data, and 40 pairs of prima
ry tumors and metastases, by p53 immunohistochemistry and temperature-
gradient gel electrophoresis. Comparison of primary tumors and their m
etastases revealed identical results in 88%-90% of the cases, indicati
ng that, in most cases, mutant p53 occurs prior to metastatic spread a
nd remains clonally conserved. With respect to all tumors, moderate/hi
gh p53 expression was significantly more prevalent in serous-papillary
types, carcinomas with high grade, and high Ki67 scores, but was not
associated with age, stage, or hormone receptor status. Kaplan-Meier a
nalysis of 83 cases, followed-up for 9-96 months, demonstrated that mo
derate/high p53 overexpression in the group of 66 stage T3/M1 tumors w
as associated significantly (P = 0.0028 and P = 0.0105) with shorter o
verall and recurrence-free survival. Multivariate analysis revealed th
at advanced clinical stage and p53 positivity were the only independen
t predictive variables. No significance was seen in regard to second-l
ook results and outcome of 50 patients receiving platinum-based chemot
herapy. These observations show that p52 immunohistochemistry is an in
dependent prognostic indicator at the given cut-off level, but does no
t reliably predict chemotherapy response.