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Clinical Trial Summary

Active Surveillance manages selected men with prostate cancer expectantly with curative intent. This means men are carefully selected and subsequently actively observed in order to have the possibility to offer them curative treatment once the tumor seems to progress.

The goal of this study is to validate the treatment option Active Surveillance in men with localized, well differentiated prostate cancer, in order to limit the amount of overtreatment. A number of key points will be studied, such as the pathological findings in radical prostatectomy specimens, and the effect of expectancy on the quality of life.


Clinical Trial Description

Objectives:

Primary

- To evaluate the equivalence of the time on active surveillance before an active treatment between group Epstein + and the expanded active surveillance group (Epstein -)

Secondary

- To evaluate the role of diffusion-weighted MRI (DW-MRI) in the initial diagnosis and the follow-up of patients under active surveillance

- To evaluate the role of BCAR-1 to predict the clinical outcome of localized prostate cancer

- To evaluate the proportion of patients who discontinued active surveillance

- To evaluate the mortality at 10, 15 and 20 years from the inclusion in the study

- To evaluate the time to radical treatment

- To evaluate the time to metastatic disease

- To evaluate patients quality of life ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01795365
Study type Interventional
Source Centre Hospitalier Universitaire Vaudois
Contact
Status Terminated
Phase N/A
Start date December 2012
Completion date July 26, 2018

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