Z. Neskovic-konstantinovic et al., Expression of epidermal growth factor receptor in breast cancer, from early stages to advanced disease, J EXP CL C, 18(3), 1999, pp. 347-355
Citations number
42
Categorie Soggetti
Oncology
Journal title
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
Epidermal growth factor receptor was determined in 106 newly diagnosed brea
st cancer patients, using the biochemical method. The group consisted of 58
patients in stage I-II, and 48 patients in stage III-IV. Although a signif
icant inverse correlation was found between EGF-R status, and ER or PR stat
us, quantitative content of EGFR did not correlate either with quantitative
ER, or PR levels. The ER/PR content was similar in all clinical stages, su
ggesting their stability during the clinical course of the disease. EGF-R c
ontent was significantly higher in stage IV, compared to stage I, while int
ermediate clinical stages and all substages did not differ according to the
EGFR content EGF-R was confirmed as a weak prognostic factor within clinic
al stages. However. in a whole group, the overall survival was significantl
y better in patients whose tumors EGF-R content was lower than 26 fmol/mg,
compared to those with higher ERF-R content. EGF-R content was highly predi
ctive for the response to systemic endocrine treatment, in metastatic breas
t cancer patients. In locally advanced breast cancer a trend towards higher
levels of EGF-R was found in inflammatory breast cancers, compared to non-
inflammatory ones. Slightly higher levels were found in responders to local
non-endocrine primacy treatments (radiotherapy with or without chemotherap
y), compared to non-responders, suggesting the possible predictive role of
EGF-R for the response to such treatments. Our results emphasized the usefu
lness of quantitative receptor determination suggesting the relative stabil
ity of EGF-R content during thp clinical course of breast cancer its: indep
endence from ER its significant predictive and weak prognostic values, and
a possible correlation with the aggressiveness of the disease, and response
to non-endocrine treatments.