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Ep-CAM expression in pancreatic and ampullary carcinomas: frequency and prognostic relevance.

Authors :
Fong, D.
Steurer, M.
Obrist, P.
Barbieri, V.
Margreiter, R.
Amberger, A.
Laimer, K.
Gastl, G.
Tzankov, A.
Spizzo, G.
Source :
Journal of Clinical Pathology. Jan2008, Vol. 61 Issue 1, p31-35. 5p. 1 Color Photograph, 3 Charts, 2 Graphs.
Publication Year :
2008

Abstract

Aims: Pancreatic adenocarcinoma is an aggressive gastrointestinal malignancy with only a few long-term survivors even after radical surgery. Patients with ampullary cancer have a better prognosis but adjuvant therapy needs further improvement. Epithelial cell adhesion molecule (Ep-CAM) is strongly expressed in a variety of epithelial cancers and represents a promising target for immunological tumour therapy. Thus, the aim of this study was to investigate Ep-CAM expression and its potential prognostic impact in pancreatic and ampullary carcinomas. Methods: Ep-CAM expression was investigated retrospectively by immunohistochemistry in paraffin-embedded primary tumour tissue samples from a series of consecutive patients with pancreatic (n = 153) and ampullary cancer (n = 34). Results: Ep-CAM overexpression was observed in 85 of 153 pancreatic cancer specimens (56%) and in 29 of 34 ampullary cancer samples (85%). Overall, Ep-CAM failed to be an independent prognostic marker. However, subgroup analyses showed that Ep-CAM overexpression correlated with shorter overall survival among patients with ampullary cancer and advanced stage pancreatic cancer. In the latter subgroup, survival gradually worsened with increasing Ep-CAM scores. Furthermore, in ampullary cancer, Ep-CAM overexpression was found to correlate with tumour stage. Conclusions: Ep-CAM overexpression was detectable in the majority of cases with pancreatic and ampullary cancer, Therefore, Ep-CAM represents an attractive target for immune-based therapeutic interventions in these tumour entities. However, the prognostic value of Ep-CAM overexpression remains undetermined. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219746
Volume :
61
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Clinical Pathology
Publication Type :
Academic Journal
Accession number :
29416456
Full Text :
https://doi.org/10.1136/jcp.2006.037333