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European Urology

European Urology

Volume 48, issue 5, pages 703-880, November 2005

Bladder Cancer

Tissue Microarray Analysis of the Prognostic Value of E-Cadherin, Ki67, p53, p27, Survivin and MSH2 Expression in Upper Urinary Tract Transitional Cell Carcinoma

Gaëlle Fromont, Morgan Rouprêt, Najla Amira, Mathilde Sibony, Guy Vallancien, Pierre Validire and Olivier Cussenot

Accepted 11 July 2005, Published online 1 August 2005, pages 764 - 770


Abstract

Objectives:

Invasive upper urinary tract transitional cell carcinoma (UUT-TCC) has a poor prognosis (survival <50% at 5 years), and tumor stage and grade often fail to predict outcome. Our purpose was to establish whether the expression of Ki67, p53, p27, E-cadherin, survivin or MSH2 can provide prognostic information in UUT-TCC.

Methods:

The following data from the files of 62 patients treated for UUT-TCC over 12 years were collated: age at diagnosis, prior history of cancer, tobacco consumption, tumor stage (including surgical margins) and grade, and disease progression. Immunohistochemistry (IHC) for Ki67, p53, p27, E-cadherin, survivin and MSH2 was performed on tissue microarray sections from tumor tissue.

Results:

Overall, 31 patients died with metastasis from UUT-TCC. Mean survival was 20 ± 16 months (range 2–83). In a univariate analysis, advanced age (>68 years), high stage, and loss of E-cadherin and high Ki67 expression were associated with a poor prognosis and disease recurrence. In a multivariate analysis, the independent factors of prognosis and recurrence were E-cadherin (p = 0.001; p = 0.004), age (p = 0.022; p = 0.008), and high stage (p = 0.023; p = 0.008).

Conclusions:

E-cadherin is a useful independent prognostic factor in UUT-TCC, for use in addition to age and tumor stage. It is of particular interest to predict recurrence in patients with low grade non-invasive tumors. Ki67 expression is informative but less significant. Survivin, p53, p27 and MSH2 have no prognostic value.

Keywords: Microarray, Prognosis, Ureter, Renal pelvis, Transitional cell carcinoma.


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