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

被引:88
作者
Fong, D. [1 ]
Steurer, M. [1 ]
Obrist, P. [2 ]
Barbieri, V. [3 ]
Margreiter, R. [4 ]
Amberger, A. [4 ]
Laimer, K. [4 ]
Gastl, G. [1 ]
Tzankov, A. [2 ]
Spizzo, G. [1 ,4 ]
机构
[1] Innsbruck Med Univ, Div Hematol & Oncol, A-6020 Innsbruck, Austria
[2] Innsbruck Med Univ, Dept Pathol, Innsbruck, Austria
[3] Innsbruck Med Univ, Dept Biostat, Innsbruck, Austria
[4] Innsbruck Med Univ, Tyrolean Canc Res Inst, Innsbruck, Austria
关键词
D O I
10.1136/jcp.2006.037333
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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 (EpCAM) 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 EpCAM 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.
引用
收藏
页码:31 / 35
页数:5
相关论文
共 26 条
[1]   KSA antigen Ep-CAM mediates cell-cell adhesion of pancreatic epithelial cells: Morphoregulatory roles in pancreatic islet development [J].
Cirulli, V ;
Crisa, L ;
Beattie, GM ;
Mally, MI ;
Lopez, AD ;
Fannon, A ;
Ptasznik, A ;
Inverardi, L ;
Ricordi, C ;
Deerinck, T ;
Ellisman, M ;
Reisfeld, RA ;
Hayek, A .
JOURNAL OF CELL BIOLOGY, 1998, 140 (06) :1519-1534
[2]   ING-1, a monoclonal antibody targeting Ep-CAM in patients with advanced adenocarcinomas [J].
de Bono, JS ;
Tolcher, AW ;
Forero, A ;
Vanhove, GFA ;
Takimoto, C ;
Bauer, RJ ;
Hammond, LA ;
Patnaik, A ;
White, ML ;
Shen, S ;
Khazaeli, MB ;
Rowinsky, EK ;
LoBuglio, AF .
CLINICAL CANCER RESEARCH, 2004, 10 (22) :7555-7565
[3]   A fully human anti-Ep-CAM scFv-beta-glucuronidase fusion protein for selective chemotherapy with a glucuronide prodrug [J].
de Graaf, M ;
Boven, E ;
Oosterhoff, D ;
van der Meulen-Muileman, IH ;
Huls, GA ;
Gerritsen, WR ;
Haisma, HJ ;
Pinedo, HM .
BRITISH JOURNAL OF CANCER, 2002, 86 (05) :811-818
[4]   Ep-CAM overexpression in breast cancer as a predictor of survival [J].
Gastl, G ;
Spizzo, G ;
Obrist, P ;
Dünser, M ;
Mikuz, G .
LANCET, 2000, 356 (9246) :1981-1982
[5]   Immunotherapy of malignant ascites with trifunctional antibodies [J].
Heiss, MM ;
Ströhlein, MA ;
Jäger, M ;
Kimmig, R ;
Burges, A ;
Schoberth, A ;
Jauch, KW ;
Schildberg, FW ;
Lindhofer, H .
INTERNATIONAL JOURNAL OF CANCER, 2005, 117 (03) :435-443
[6]  
HIMMLER M, 2005, J CLIN ONCOL S1, V23, P2555
[7]   MUC1 and MUC2 in pancreatic neoplasia [J].
Levi, E ;
Klimstra, DS ;
Adsay, NV ;
Andea, A ;
Basturk, O .
JOURNAL OF CLINICAL PATHOLOGY, 2004, 57 (05) :456-462
[8]   Epithelial cell adhesion molecule (Ep-CAM) modulates cell-cell interactions mediated by classic cadherins [J].
Litvinov, SV ;
Balzar, M ;
Winter, MJ ;
Bakker, HAM ;
BriairedeBruijn, I ;
Prins, F ;
Fleuren, GJ ;
Warnaar, SO .
JOURNAL OF CELL BIOLOGY, 1997, 139 (05) :1337-1348
[9]  
Litvinov SV, 1996, AM J PATHOL, V148, P865
[10]   Expression of the 17-1A antigen in gastric and gastro-oesophageal junction adenocarcinomas: a potential immunotherapeutic target? [J].
Martin, IG ;
Cutts, SG ;
Birbeck, K ;
Gray, S ;
Quirke, P .
JOURNAL OF CLINICAL PATHOLOGY, 1999, 52 (09) :701-704