K. Uegaki et al., CLINICOPATHOLOGICAL SIGNIFICANCE OF EPIDERMAL GROWTH-FACTOR AND ITS RECEPTOR IN HUMAN PANCREATIC-CANCER, Anticancer research, 17(5B), 1997, pp. 3841-3847
The expression of epidermal growth factor (EGF) and its receptor (EGF-
R) was examined immunohistochemically in 60 primary and 26 metastatic
lesions of pancreatic carcinoma. EGF was stained mainly in the cytopla
sm of tumor cells, and EGF-R was stained mainly on the surface of cell
s. The expression rates of EGF and EGF-R were 28% and 43% for primary
lesions, and 46% and 46% for metastatic lesions, respectively. The exp
ression of EGF and EGF-R alone did not correlate with any clinicopatho
logical factors such as clinical stage, tumor size, nodal involvement,
histology, etc. The median survival period after pancreatectomy was 2
1.4 months for patients with EGF(+) cancers and 25.1 months for those
with EGF (-) ones. On the other hand the median survival period was 22
.7 months for patients with EGF-R (+) cancers and 25.0 months for thos
e with EGF-R (-) cancers. There were no significant differences in sur
vival between groups of patients differing in EGF or EGF-R expression.
When the expression of EGF and EGF-R was analysed in combination, the
survival curve of patients with EGF(+) and EGF-R(+) cancers was found
to be lower than that of the rest of the patients (p=0.07), and espec
ially the survival curve of patients with EGF(+)EGF-R(+) cancers was s
ignificantly lower than that of patients with EGF(+)EGF-R(-) cancers (
p=0.02), and EGF(-)EGF-R(+) cancers (p=0.06). These results indicate t
hat the expression of EGF or EGF-R alone in pancreatic cancer does not
reflect the prognosis of patients; however the coexpression of EGF an
d EGF-R may be a beneficial prognostic factor for pancreatic cancer.