PRIMARY CHEMOTHERAPY IN BREAST INVASIVE-CARCINOMA - PREDICTIVE VALUE OF THE IMMUNOHISTOCHEMICAL DETECTION OF HORMONAL RECEPTORS, P53, C-ERBB-2, MIB1, PS2 AND GST-PI
G. Macgrogan et al., PRIMARY CHEMOTHERAPY IN BREAST INVASIVE-CARCINOMA - PREDICTIVE VALUE OF THE IMMUNOHISTOCHEMICAL DETECTION OF HORMONAL RECEPTORS, P53, C-ERBB-2, MIB1, PS2 AND GST-PI, British Journal of Cancer, 74(9), 1996, pp. 1458-1465
Primary chemotherapy in operable breast invasive carcinoma enables tum
our reduction and conservative surgery. In order to search for one or
more biological factors capable of predicting tumour behaviour under p
rimary chemotherapy, and subsequent patient survival, an immunohistoch
emical study was performed with specific antibodies to p53, c-erbB-2 (
Her-2/neu), Mib1 (antiKi-67), pS2, GST pi, oestrogen receptors (ERs) a
nd progesterone receptors (PRs). Core biopsies, obtained before primar
y chemotherapy, were available from a series of 128 breast invasive ca
rcinomas treated between January 1985 and April 1989, with a median fo
llow-up of 93.3 months. Univariate statistical analysis showed that ne
gative ER detection by immunohistochemistry (IHC) was highly correlate
d with chemosensitivity (P=0.001). A high percentage of Mib1-positive
tumour cells (>40%), as well as initial tumour size less than 4 cm, we
re also correlated with tumour responsiveness to chemotherapy (P=0.009
and P=0.03). By multivariate analysis IHC-ER, Mib1 and initial tumour
size were independent predictors, the last parameter being the most i
mportant. Concerning subsequent patient survival, c-erbB-2 overexpress
ion, as detected by IHC, was significant with respect to overall survi
val (OS) (P=0.0006), disease-free interval (DFI) (P=0.03) and metastas
is-free interval (MFI) (P=0.008) by univariate analysis. Furthermore,
c-erbB-2 was the major independent prognostic factor for OS and MFI by
multivariate analysis.