Medical Economics of Urinary PCA3 Test for Prostate Cancer Diagnosis
Patients Scheduled for Prostate Biopsy Because of Increased Serum PSA and/or Abnormal Digital Rectal Examination
About this trial
This is an interventional diagnostic trial for Patients Scheduled for Prostate Biopsy Because of Increased Serum PSA and/or Abnormal Digital Rectal Examination focused on measuring diagnosis, prostate cancer, urine, medical economics
Eligibility Criteria
Inclusion Criteria:
- patients ≥ 18 year-old
- patients who undergo prostate biopsy for increased serum PSA and/or abnormal digital rectal examination
- patients who gave informed consent
Exclusion Criteria:
- no informed consent
- medical history of or current significant prostate cancer
- medical history of or current extra-prostatic cancer
- high risk of loss of follow-up
- clinically obvious prostate cancer (clinical stage ≥ T3, PSA ≥ 50 ng/ml, lymph node involvement, osteolytic bone metastases)
Sites / Locations
- CHU Angers
- Centre Hospitalier Alpes Leman
- Hôpital du Bocage
- Hôpital Edouard Herriot
- Hôpital Pitié-Salpêtrière,
- Hôpital Tenon
- Centre Hospitalier Lyon Sud
- Hôpital de la Milétrie
- Centre hospitalier de Thonon les bains
- Centre Hospitalier de Valence
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Results of urinary PCA3 test will be available
Results of urinary PCA3 test will not be available
In this arm, physicians will have knowledge of urinary PCA3 test results. How they subsequently manage patients with prostate cancer suspicion is likely to be influenced by urinary PCA3 test results
In this arm, physicians will not have knowledge of urinary PCA3 test results. How they subsequently manage patients with prostate cancer suspicion will therefore not be influenced by urinary PCA3 test results