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Volume 18, Issue 4, Pages 357-365 (December 2009)


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Loss of Bcl-2 expression in colon cancer: A prognostic factor for recurrence in stage II colon cancer

Laurent PoinclouxabCorresponding Author Informationemail address, Xavier Durandoc, Jean François Seitzb, Emilie Thivatc, Valérie-Jeanne Bardoud, Marie-Hélène Giovanninid, Danièle Parriauxe, Nicolas Barriereb, Marc Giovanninib, Jean-Robert Delperob, Geneviève Mongese

Accepted 27 September 2008.

Abstract 

Aims

To evaluate the prognostic value of immunohistochemical expression of Bcl-2 in colon cancers.

Patients and methods

Two hundred and twenty-six resected and paraffin-embedded colon carcinomas were analysed by immunostaining using monoclonal antibodies for Bcl-2. We evaluated whether the Bcl-2 staining patterns, semi-quantitatively assessed, could be correlated with the pTNM stage, size and tumour circumference, differentiation, appearance, vascular invasion, perineural invasion, colloid component, margins, involvement of adjacent structures, stromal appearance, flow cytometry and the S-phase.

Results

Eighty patients (36%) were considered Bcl-2 positive. The extent of Bcl-2 expression by tumour cells decreased significantly with respect to increasing tumour size (P=0.042), the extension of parietal invasion pT (P=0.007), the invasive nature of the tumour (P=0.024), and extent of the circumference (P=0.024). In a multivariate analysis, Bcl-2 expression does not appear as an independent prognosis factor in the overall population as in the 166 patients with optimal resection. Of the 59 stage II patients, using univariate analysis, Bcl-2 appears to be predictive of relapse-free survival (P=0.025) but not of overall survival (P=0.09).

Conclusion

The loss of Bcl-2 expression appears to be correlated with increase in number of relapses in the stage II colon cancers and could be a potential useful additional histo-prognostic marker in therapy decision making. Bcl-2 immunodetection seems to be associated with slower local tumour growth.

a Department of Gastroenterology CHRU, Hotel-Dieu, avenue Vercingetorix, 63000 Clermont-Ferrand, France

b Department of Digestive Oncology, Institut Paoli Calmettes, 232 boulevard Sainte Marguerite, Marseille, France

c Clinical Research Unit, Centre Jean Perrin, 58 rue Montalembert, 63011 Clermont-Ferrand, France

d Department of Biostatistics, Institut Paoli Calmettes, 232 boulevard Sainte Marguerite, Marseille, France

e Department of Pathology, Institut Paoli Calmettes, 232 boulevard Sainte Marguerite, Marseille, France

Corresponding Author InformationCorresponding author. Department of Gastroenterology CHRU, Hotel-Dieu, avenue Vercingetorix, 63000 Clermont-Ferrand, France. Tel.: +33 4 73 75 05 44; fax: +33 4 73 75 05 07.

PII: S0960-7404(08)00101-1

doi:10.1016/j.suronc.2008.09.003


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