Andersen J, Thorpe S M, King W J, Rose C, Christensen I, Rasmussen B B, Poulsen H S
Department of Pathology, Rigshospitalet, København O, Denmark.
Eur J Cancer. 1990 Apr;26(4):442-9. doi: 10.1016/0277-5379(90)90013-j.
Estrogen receptors (ER) were independently analyzed using dextran-coated charcoal assays (ER-DCC) and immunohistochemical assays in frozen (ER-ICA) and paraffin-embedded tissue (ER-PAR) from 130 human breast cancer specimens drawn from postmenopausal high-risk patients registered in the Danish Breast Cancer Cooperative Group. ER was best detected with the ER-DCC assay followed by the ER-ICA (relative sensitivity 87%) and the ER-PAR assays (relative sensitivity 71%). The semiquantified staining features of the immunohistochemical assays were statistically significantly correlated with each other and with ER-DCC. Analysis of disease-free interval (DFI) and overall survival (OS) showed that all assays allowed statistically significant discrimination between a high risk and a low risk group, although the sensitivity differences tended to be reflected as small differences in clinical discriminatory power. The patient groups were then stratified according to adjuvant treatment [radiotherapy (RT) versus radiotherapy and tamoxifen (RT + TAM)]. The survival advantage was tied primarily to the receptor status itself in the steroid-binding assays, but was linked to both the receptor status and the adjuvant treatment in the immunohistochemical assays. Thus, the relative risks in terms of DFI and OS were of the same relative magnitude in the RT and RT + TAM groups for ER-DCC assays using a cut-off level of 10 fmol/mg cytosol protein, while there were large differences in the relative risks between RT and RT + TAM groups for ER-ICA and ER-PAR assays. We conclude that an ER assay in fresh tissue should be given first priority, but if there is no fresh tissue, an ER assay in paraffin-embedded tissue offers a reasonably good alternative as a prognosticator and an equivalent alternative as a predictor of the response to endocrine treatment.
采用葡聚糖包被活性炭分析法(ER-DCC)以及免疫组织化学分析法,分别对来自丹麦乳腺癌协作组登记的绝经后高危患者的130例人类乳腺癌标本的冷冻组织(ER-ICA)和石蜡包埋组织(ER-PAR)中的雌激素受体(ER)进行独立分析。ER-DCC分析法检测ER的效果最佳,其次是ER-ICA分析法(相对灵敏度87%)和ER-PAR分析法(相对灵敏度71%)。免疫组织化学分析法的半定量染色特征相互之间以及与ER-DCC均具有显著的统计学相关性。无病生存期(DFI)和总生存期(OS)分析显示,尽管灵敏度差异在临床鉴别能力上表现为较小差异,但所有分析方法均能在高危组和低危组之间进行具有统计学意义的区分。然后根据辅助治疗方法[放疗(RT)与放疗加他莫昔芬(RT + TAM)]对患者组进行分层。在类固醇结合分析中,生存优势主要与受体状态本身相关,但在免疫组织化学分析中则与受体状态和辅助治疗均相关。因此,对于使用10 fmol/mg胞浆蛋白临界值的ER-DCC分析,RT组和RT + TAM组在DFI和OS方面的相对风险具有相同的相对大小,而对于ER-ICA和ER-PAR分析,RT组和RT + TAM组之间的相对风险存在较大差异。我们得出结论,新鲜组织中的ER分析应优先考虑,但如果没有新鲜组织,石蜡包埋组织中的ER分析作为预后指标是一个相当不错的选择,作为内分泌治疗反应的预测指标也是一个等效的选择。