IMMUNOHISTOCHEMICAL DETECTION OF SEX STEROID-RECEPTORS IN BREAST-CANCER USING ROUTINE PARAFFIN SECTIONS - COMPARISON WITH FROZEN-SECTIONS AND ENZYME-IMMUNOASSAY
Jm. Elias et al., IMMUNOHISTOCHEMICAL DETECTION OF SEX STEROID-RECEPTORS IN BREAST-CANCER USING ROUTINE PARAFFIN SECTIONS - COMPARISON WITH FROZEN-SECTIONS AND ENZYME-IMMUNOASSAY, Journal of cellular biochemistry, 1994, pp. 126-133
Estrogen and progesterone receptors (ER and PR) on 48 surgically remov
ed breast cancers were evaluated by three methods: immunoenzymatic (ER
/PR-EIA), immunohistochemical in frozen sections (ER/PR-ICA), and immu
nohistochemical in paraffin sections (ER/PR-PAR). The monoclonal antib
odies H222 and KD68 were used for immunohistochemical detection of ER
and PR, respectively. Immunohistochemical stains for pS2, an estrogen-
regulated protein, were also done for compatibility with previous ER/P
R-PAR studies. We assessed concordance with chi-square and Pearson's c
orrelation coefficient. We concluded that ER/PR-PAR is the least sensi
tive of the three assays (90.9% ER, 88.5% PR) and, until appropriate t
echnical and clinical validation is achieved, should not be used as a
first-line assay. Also, because of this lower sensitivity, we recommen
d that pS2 evaluation always accompany ER/PR-PAR to facilitate distinc
tion between clinical negatives and those due to irretrievably lost im
munoreactivity. We also conclude that ER/PR-ICA is a good semiquantita
tive method that, in combination with ER/PR-EIA, most accurately asses
ses receptor status. (C) 1994 Wiley-Liss, Inc.