Department of Obstetrics and Gynecology, University Medical Center of the Johannes Gutenberg-University, Langenbeckstr. 1, 55131, Mainz, Germany.
Breast Cancer Res Treat. 2011 Feb;125(3):637-46. doi: 10.1007/s10549-010-0856-5. Epub 2010 Mar 30.
Epithelial cell adhesion molecule (Ep-CAM) recently received increased attention as a prognostic factor in breast cancer. We aimed to validate the influence of Ep-CAM RNA expression in untreated node-negative breast cancer. Ep-CAM RNA expression was evaluated utilizing microarray-based gene-expression profiling in 194 consecutive node-negative breast cancer patients with long-term follow-up not treated in the adjuvant setting. The prognostic significance of Ep-CAM RNA expression for disease-free survival (DFS), metastasis-free survival (MFS), and breast cancer-specific overall survival (OS) was evaluated in univariate and multivariate analysis adjusted for age, grading, pTstage, ER as well as PR receptor and HER-2 status. Additionally, Ep-CAM RNA expression was compared with immunohistochemistry (IHC) for Ep-CAM in 194 patients. The prognostic impact of Ep-CAM gene expression was validated in further 588 node-negative breast cancer patients. Levels of Ep-CAM RNA expression showed a significant correlation with IHC (P = 0.001) and predicted in univariate analysis DFS (P = 0.001, HR = 2.4), MFS (P = 0.003, HR = 2.5), and OS (P = 0.002, HR = 3.1) accurately. The prognostic influence of Ep-CAM RNA was significant also in multivariate analysis for DFS (P = 0.017, HR = 2.0), MFS (P = 0.049, HR = 1.9), and OS (P = 0.042, HR = 2.3), respectively. The association with MFS was confirmed in an independent validation cohort in univariate (P = 0.006, HR = 1.9) and multivariate (P = 0.035, HR = 1.7) analysis. Ep-CAM RNA correlated with the proliferation metagene (P < 0.001, R=0.425) Nevertheless, in multivariate analysis, Ep-CAM was associated with MFS independent from the proliferation metagene (P = 0.030, HR = 1.8). In conclusion, Ep-CAM RNA expression is associated with poor MFS in three cohorts of untreated node-negative breast cancer.
上皮细胞黏附分子(Ep-CAM)最近作为乳腺癌的预后因素受到了越来越多的关注。我们旨在验证 Ep-CAM RNA 表达在未经治疗的淋巴结阴性乳腺癌中的影响。我们利用基于微阵列的基因表达谱分析了 194 例连续的淋巴结阴性乳腺癌患者,这些患者未经辅助治疗,且具有长期随访,无疾病生存(DFS)、无转移生存(MFS)和乳腺癌特异性总生存(OS)的预后意义在调整年龄、分级、pT 分期、ER 以及 PR 受体和 HER-2 状态的单变量和多变量分析中进行了评估。此外,还比较了 194 例患者中 Ep-CAM RNA 表达与免疫组织化学(IHC)检测 Ep-CAM 的结果。在另外 588 例淋巴结阴性乳腺癌患者中验证了 Ep-CAM 基因表达的预后影响。Ep-CAM RNA 水平与 IHC 呈显著相关性(P=0.001),在单变量分析中准确预测 DFS(P=0.001,HR=2.4)、MFS(P=0.003,HR=2.5)和 OS(P=0.002,HR=3.1)。Ep-CAM RNA 的预后影响在多变量分析中也有意义DFS(P=0.017,HR=2.0)、MFS(P=0.049,HR=1.9)和 OS(P=0.042,HR=2.3)。在单变量(P=0.006,HR=1.9)和多变量(P=0.035,HR=1.7)分析中,MFS 的关联在独立验证队列中得到了证实。Ep-CAM RNA 与增殖代谢基因(P<0.001,R=0.425)相关。然而,在多变量分析中,Ep-CAM 与 MFS 相关,与增殖代谢基因无关(P=0.030,HR=1.8)。总之,Ep-CAM RNA 表达与未经治疗的淋巴结阴性乳腺癌三组患者的不良 MFS 相关。