Correlation of β-catenin, but not PIN1 and cyclin D1, overexpression with disease-free and overall survival in patients with cancer of the parotid gland

ABSTRACT Background Malignant tumors of the salivary glands comprise about 3% to 5% of all head and neck carcinomas. The purpose of our study was to find possible predictive and/or prognostic markers for parotid cancer. Methods A total of 46 tissue samples of carcinomas of the parotid gland were imm...

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Published inHead & neck Vol. 37; no. 1; pp. 30 - 36
Main Authors Lill, Claudia, Schneider, Sven, Seemann, Rudolf, Kadletz, Lorenz, Aumayr, Klaus, Ghanim, Bahil, Thurnher, Dietmar
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.01.2015
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Summary:ABSTRACT Background Malignant tumors of the salivary glands comprise about 3% to 5% of all head and neck carcinomas. The purpose of our study was to find possible predictive and/or prognostic markers for parotid cancer. Methods A total of 46 tissue samples of carcinomas of the parotid gland were immunohistochemically stained for ß‐catenin, cyclin D1, and PIN1. The factors were analyzed regarding their prognostic value for disease‐free and overall survival. Results An overexpression of the cytoplasmatic ß‐catenin was linked to a statistically significant worse outcome regarding disease‐free (p = .0296) and overall survival (p = .0416). The 5‐year overall survival was 83.9% in patients without and 0% in patients presenting with overexpression of cytoplasmatic ß‐catenin. Additionally, Union Internationale Contre le Cancer (UICC) stage correlated with overall survival (p = .0306) and disease‐free survival (DFS; p = .0473). Conclusion Multivariate analysis showed that overexpression of cytoplasmatic ß‐catenin and the UICC stage are 2 independent prognostic markers for survival in patients with parotid cancer. © 2014 Wiley Periodicals, Inc. Head Neck 37: 30–36, 2015
Bibliography:ark:/67375/WNG-W56Z8DVL-R
istex:AB9ACA991E436A9D1F6F1BAD1133C7BB2DB34A57
ArticleID:HED23546
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1043-3074
1097-0347
DOI:10.1002/hed.23546