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Clinical Trials/NCT00427817
NCT00427817
Completed
Not Applicable

PRO-STATE: Prognostic Interest of Serum Protein Profiles of Patients Undergoing a Prostate Biopsy: Search for a Profile Corresponding to Fast-developing Lesions and Characterization of Implicated Proteins.

University Hospital, Grenoble1 site in 1 country300 target enrollmentAugust 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Adenoma, Prostatic
Sponsor
University Hospital, Grenoble
Enrollment
300
Locations
1
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The main objective of this study is to realise serum protein profiles for each patient undergoing a prostate biopsy and to identify relevant proteins.

Detailed Description

In men, prostate carcinoma is the first cancer and the second cause of death by cancer. It is a slowly evolving disease with no prognostic marker of poor outcome. Currently, the Prostate Specific Antigen (PSA) is the only available biological marker. It is a tissue marker and not a tumoral pathology control. This is why new tissue markers are urgently needed to select patients with unfavourable evolution, in order to treat them rapidly by more effective methods such as chemotherapy, hormonotherapy or radiotherapy. This could improve survival time and quality of life. Proteomic and clinical data comparison could point to new relevant molecules and permit the development of new biological tests for routine use. SELDI-TOF-MS (Surface Enhanced Laser Desorption/Ionisation Mass Spectrometry) permits an extremely sensitive analysis of proteins. This method has been substantially ratified by the literature and a number of markers have already been identified, particularly for several cancer pathologies. As far as prostate carcinomas are concerned, previous proteomic researches on serum have led to diagnostic parameters, differentiating healthy patients, patients with benign lesion and patients having malignant lesions. However, at present, no relevant protein has been identified. Moreover, no study has been carried out to characterize fast-developing lesions, in order to anticipate response to treatments. The main objective of this study is to realise serum protein profiles for each patient undergoing a prostate biopsy and to identify relevant proteins. The main judgement criteria will be intensity peaks in the protein profile (area and height) with reference to combined criteria (PSA rate, clinical stage, Gleason score). Two groups will be compared: * Group 1: Control (negative biopsy). * Group 2: Prostate carcinoma (positive biopsy). This group will be subdivided: * Group 2a : favourable prognostic according to AMICO classification * Group 2b : intermediate or unfavourable prognostic according to AMICO classification This will contribute to setting up an aftercare database combining clinical data with biological data and protein profile.

Registry
clinicaltrials.gov
Start Date
August 2006
End Date
January 2011
Last Updated
14 years ago
Study Type
Observational
Sex
Male

Investigators

Sponsor
University Hospital, Grenoble
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient undergoing a prostate biopsy or a prostatectomy(according to common criteria).
  • Exclusion criteria:
  • Patient refusing to take part in the study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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