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PMID: 15567937 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

High Ep-CAM expression is associated with poor prognosis in node-positive breast cancer.

Breast cancer research and treatment ·Vol. 86 ·No. 3 ·2004-08-00 ·Pages 207-13

Spizzo G, Went P, Dirnhofer S, Obrist P, Simon R, Spichtin H, Maurer R, Metzger U, von Castelberg B, Bart R, Stopatschinskaya S, Köchli OR, Haas P, Mross F, Zuber M, Dietrich H, Bischoff S, Mirlacher M, Sauter G, Gastl G

Abstract

Previous studies in small series of patients with invasive breast cancer suggested a prognostic value of Ep-CAM overexpression in primary tumor tissue. To corroborate these findings, we performed a retrospective analysis of Ep-CAM expression using a tissue microarray containing tissue specimens from a large patient set. Ep-CAM expression was evaluated by immunohistochemistry in breast cancer tissue from 1715 patients with documented raw survival data. High level Ep-CAM expression (overexpression) was found in 41.7% of tumor samples, low level expression was found in 48.0% and no expression in 10.3% of tumor samples. Ep-CAM expression predicted poor overall survival in this patient cohort (p < 0.0001). Overall survival decreased significantly with increasing Ep-CAM expression. However, in this patient sample Ep-CAM expression was not an independent prognostic marker by multivariate analysis. Subgroup analysis revealed that Ep-CAM expression was a prognostic marker in node-positive (p < 0.0001) but not in node-negative (p = 0.58) breast cancer patients. Intriguingly, Ep-CAM expression was predictive for a dismal prognosis in patients receiving adjuvant cytotoxic (p = 0.03) or hormonal therapy (p < 0.0001) but not in untreated patients (p = 0.41). In summary, this study provides strong evidence that expression of Ep-CAM is a powerful marker of poor prognosis in node-positive invasive breast carcinoma and a potential predictive marker of sensitivity to adjuvant hormonal and/or cytotoxic treatment modalities.

MeSH Terms
Aged Antigens, Neoplasm/biosynthesis Antineoplastic Combined Chemotherapy Protocols/therapeutic use Biomarkers, Tumor Breast Neoplasms/drug therapy,genetics,pathology CD3 Complex Carcinoma/drug therapy,genetics,pathology Cell Adhesion Molecules/biosynthesis Epithelial Cell Adhesion Molecule Female Gene Expression Profiling Humans Immunohistochemistry Lymphatic Metastasis Middle Aged Prognosis Retrospective Studies Survival Analysis Treatment Outcome
Chemicals
Antigens, Neoplasm Biomarkers, Tumor CD3 Complex Cell Adhesion Molecules Epithelial Cell Adhesion Molecule
Authors & Affiliations
20 authors, click to expand affiliations / ORCID
Spizzo Gilbert
Division of Haematology and Oncology, University of Innsbruck, Innsbruck, Austria.
Went Philip
Dirnhofer Stephan
Obrist Peter
Simon Ronald
Spichtin Hanspeter
Maurer Robert
Metzger Urs
von Castelberg Brida
Bart Rahel
Stopatschinskaya Shanna
Köchli Ossi Robert
Haas Philip
Mross Friedrich
Zuber Markus
Dietrich Holger
Bischoff Susanne
Mirlacher Martina
Sauter Guido
Gastl Guenther
Article Info
Journal
Breast cancer research and treatment
Abbr.
Breast Cancer Res Treat
ISSN
0167-6806
Published
2004-08-00
Pages
207-13
Language
English
Region
Netherlands
NLM ID
8111104
Subset
IM
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