Research Papers:
Human epidermal growth factor receptor 2 expression is more important than Bacillus Calmette Guerin treatment in predicting the outcome of T1G3 bladder cancer
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Abstract
Luigi Cormio1,*, Francesca Sanguedolce2,*, Antonella Cormio3, Paolo Massenio1, Maria Carmela Pedicillo2, Simona Cagiano2, Giuseppe Calò1, Vincenzo Pagliarulo4, Giuseppe Carrieri1,**, Pantaleo Bufo2,**
1Department of Urology, University Hospital of Foggia, Foggia, Italy
2Department of Pathology, University Hospital of Foggia, Foggia, Italy
3Department of Biosciences, Biotechnologies, and Biopharmaceutics, University of Bari, Bari, Italy
4Department of Urology, University Hospital of Bari, Bari, Italy
*These authors have contributed equally to this work
**These authors share senior authorship
Correspondence to:
Francesca Sanguedolce, email: [email protected]
Keywords: non-muscle-invasive bladder cancer, HER-2, immunohistochemistry, prognosis
Received: October 02, 2016 Accepted: February 06, 2017 Published: March 07, 2017
ABSTRACT
In the present study we tested the role of Human Epidermal Growth Factor Receptor-2 (HER-2) expression, as assayed by immunohistochemistry, in predicting recurrence and progression in 67 patients with T1G3 BC having undergone transurethral resection of bladder tumor (TURBT) alone (33) or TURBT + Bacillus Calmette Guerin (BCG) instillations (34). All patients had a negative restaging TURBT within 4 months after the first TURBT. At median follow-up of 75.7 months, the overall disease-free and progression-free rates were 35.8% and 73.0%, respectively. Univariate Kaplan-Meier survival analysis showed that traditional prognostic factors (sex, tumor number/size/recurrence) failed to predict disease-free and progression free survival (DFS, PFS). BCG treatment was a significant predictor of DFS (p=0.0231) but not of PFS (p=0.6901). HER-2 overexpression was a significant predictor of DFS (p=0.0013) and PFS (p=0.0322) in the overall patients population, but failed to predict PFS when patients were stratified for treatment (BCG: p=0.1290; no BCG: p=0.1696) probably due to the limited number of events. Multivariate Cox proportional-hazards regression analysis confirmed that BCG treatment was a significant predictor of DFS (p=0.012) but not of PFS (p=0.924), whereas HER-2 overexpression was a significant predictor of DFS (p=0.001) and PFS (p=0.041). These findings suggest that HER-2 status performs better than “traditional” prognostic factors as well as of BCG treatment in predicting the outcome of T1G3 BC, thus providing grounds for further testing this marker and possibly incorporating it in a panel of molecular markers that could reliably predict the behavior of this challenging disease.
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