Gene expression signatures predict outcome in non-muscle invasive bladder carcinoma:: A multicenter validation study

被引:160
作者
Dyrskjot, Lars
Zieger, Karsten
Real, Francisco X.
Malats, Nuria
Carrato, Alfredo
Hurst, Carolyn
Kotwal, Sanjeev
Knowles, Margaret
Malmstrom, Per-Uno
de la Torre, Manuel
Wester, Kenneth
Allory, Yves
Vordos, Dirnitri
Caillault, Aurelie
Radvanyi, Francois
Hein, Anne-Mette K.
Jensen, Jens L.
Jensen, Klaus M. E.
Marcussen, Niels
Orntoft, Torben F. [1 ]
机构
[1] Aarhus Univ Hosp, Dept Clin Biochem, Mol Diagnost Lab, Skejby, Denmark
[2] Aarhus Univ Hosp, Dept Urol, Skejby, Denmark
[3] Aarhus Univ Hosp, Dept Theoret Stat, Skejby, Denmark
[4] Inst Municipal Invest Med, E-08003 Barcelona, Spain
[5] Univ Pompeu Fabra, Ctr Res Environm Epidemiol, Barcelona, Spain
[6] Canc Res UK Clin Ctr, Leeds, W Yorkshire, England
[7] St James Univ Hosp, Pyrah Dept Urol, Leeds, W Yorkshire, England
[8] Univ Hosp, Dept Urol, Uppsala, Sweden
[9] Univ Hosp, Dept Genet & Pathol, Uppsala, Sweden
[10] Hop Henri Mondor, F-94010 Creteil, France
[11] Inst Curie, CNRS, UMR144, F-75231 Paris, France
[12] Odense Univ Hosp, Dept Clin Pathol, DK-5000 Odense, Denmark
关键词
D O I
10.1158/1078-0432.CCR-06-2940
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Clinically useful molecular markers predicting the clinical course of patients diagnosed with non-muscle-invasive bladder cancer are needed to improve treatment outcome. Here, we validated four previously reported gene expression signatures for molecular diagnosis of disease stage and carcinoma in situ (CIS) and for predicting disease recurrence and progression. Experimental Design: We analyzed tumors from 404 patients diagnosed with bladder cancer in hospitals in Denmark, Sweden, England, Spain, and France using custom microarrays. Molecular classifications were compared with pathologic diagnosis and clinical outcome. Results: Classification of disease stage using a 52-gene classifier was found to be highly significantly correlated with pathologic stage (P < 0.001). Furthermore, the classifier added information regarding disease progression of T-a or T-1 tumors (P < 0.001). The molecular 88-gene progression classifier was highly significantly correlated with progression-free survival (P < 0.001) and cancer-specific survival (P = 0.001). Multivariate Cox regression analysis showed the progression classifier to be an independently significant variable associated with disease progression after adjustment for age, sex, stage, grade, and treatment (hazard ratio, 2.3; P = 0.007). The diagnosis of CIS using a 68-gene classifier showed a highly significant correlation with histopathologic CIS diagnosis (odds ratio, 5.8; P < 0.001) in multivariate logistic regression analysis. Conclusion:This multicenter validation study confirms in an independent series the clinical utility of molecular classifiers to predict the outcome of patients initially diagnosed with non-muscle-invasive bladder cancer. This information may be useful to better guide patient treatment.
引用
收藏
页码:3545 / 3551
页数:7
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