A. Sgambato et al., CLINICAL PREDICTIVE VALUE OF P53 AND C-ERBB-2 OVEREXPRESSION IN 54 PATIENTS WITH TRANSITIONAL-CELL CARCINOMA (TCC) OF THE URINARY-BLADDER, Journal of experimental & clinical cancer research, 13(4), 1994, pp. 323-330
Various reports reveal that mutations of the p53 tumor suppressor gene
and of the c-erbB-2 proto-oncogene occur in Transitional Cell Carcino
mas (TCC) of the bladder, and that they correlate with the established
prognostic factors (particularly tumor grading and stage), suggesting
their possible clinical use in defining patients prognosis. The aim o
f this study was to confirm the hypothesis that altered expression pat
terns of the p53 tumor suppressor gene and of the c-erbB-2 oncogene ar
e associated with disease progression and clinical outcome in bladder
TCSS. We examined tissue specimens from surgical resection in 54 patie
nts with primary TCCs of the bladder. Nuclear overexpression of p53 an
d membrane staining of c-erbB-2 were evaluated by immunohistochemical
analysis and the results were correlated with the following parameters
: patient age, tumor grading and stage, nodal status, vascular and lym
phatic invasion. In our study p53 overexpression was more frequent in
invasive (pT2-pT3-pT4) than in superficial (pTa-pT1) tumors, and there
were significantly more p53 positive cases in G3 than in G1-G2 cancer
s. A weaker association was observed for lymphatic and venous invasion
. C-erbB-2 overexpression showed a weak correlation with tumor grading
, stage, nodal status, lymphatic and venous invasion. In univariate su
rvival analysis, p53 overexpression was significantly correlated with
poor outcome (p=0.0000), while c-erbB-2 showed a much weaker relations
hip with patient survival distribution (p=0,039). In multivariate anal
ysis, c-erbB-2 overexpression showed no prognostic value, while p53 sh
owed a high prognostic value with respect to the fundamental clinico-p
athological parameters. Our results confirm that p53 immunoreactivity
may be of clinical use to define bladder TCC patients subgroups of dif
ferent prognosis; on the contrary, c-erbB-2 seems to be less valuable
in defining patient outcome.