Cytoplasmic expression of β-catenin is an independent predictor of progression of conventional renal cell carcinoma: a simple immunostaining score

Aims The aims of this study were to investigate the potential of β-catenin as a biomarker for predicting cancer-specific survival, and to find a reproducible mode of evaluation of immunohistochemistry. Methods and results β-Catenin expression was analysed by immunohistochemistry in a cohort of 488 p...

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Hauptverfasser: Kovacs, Gyula (VerfasserIn) , Kaerger, Nina (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2017
In: Histopathology
Year: 2017, Jahrgang: 70, Heft: 2, Pages: 273-280
ISSN:1365-2559
DOI:10.1111/his.13059
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1111/his.13059
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/his.13059
Volltext
Verfasserangaben:Gyula Kovacs, Nina Kaerger Billfeldt, Nelli Farkas, Timea Dergez, Andras Javorhazy, Daniel Banyai, Csaba Pusztai & Arpad Szanto

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520 |a Aims The aims of this study were to investigate the potential of β-catenin as a biomarker for predicting cancer-specific survival, and to find a reproducible mode of evaluation of immunohistochemistry. Methods and results β-Catenin expression was analysed by immunohistochemistry in a cohort of 488 patients with conventional renal cell carcinoma (RCC) operated on between 2000 and 2010. The association between β-catenin expression and cancer-specific survival was assessed with univariate and multivariate Cox regression models in relation to conventional clinical pathological prognostic factors, and by Kaplan-Meier survival analysis with the log rank test. The univariate Cox regression model revealed an association of cytoplasmic β-catenin positivity and pathological variables with cancer-specific death. The multivariate Cox regression model analysis of tumours without metastatic disease at the first presentation identified the T-classification (P < 0.001) and cytoplasmic β-catenin positivity as risk factors for postoperative tumour progression. Specifically, cytoplasmic β-catenin expression was an independent factor indicating an unfavourable prognosis, with a four-fold higher risk of cancer-specific death (relative risk 4.017; 95% confidence interval 2.489-6.482; P < 0.001). The median survival time for patients with tumours showing cytoplasmic accumulation of β-catenin was 48 months, whereas the overall survival time was 166 months. Conclusions Cytoplasmic β-catenin expression is an independent prognostic factor for conventional RCC, and may help to identify patients with a high risk of cancer-specific death and to direct optimized active surveillance or adjuvant therapy. 
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