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Clinical Trials/NCT03431753
NCT03431753
Unknown
N/A

Early and Accurate Detection of Prostate Cancer in General Practice Using Novel Molecular Biomarkers and Multiparametric MR Imaging.

Aarhus University Hospital1 site in 1 country3,000 target enrollmentJanuary 1, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Aarhus University Hospital
Enrollment
3000
Locations
1
Primary Endpoint
Proportion of PC suspicious lesions detected by mpMRI based on the STHLM3 test vs. the prostate specific antigen test.
Last Updated
4 years ago

Overview

Brief Summary

Prostate cancer (PC) is the most common malignancy (4500 new cases/year) and the second leading cause of cancer-associated mortality (1200 deaths/year) among men in Denmark. PC is generally diagnosed on the basis of an elevated prostate specific antigen blood test followed by transrectal ultrasound (TRUS)-guided prostate biopsy.

This study aims to test early detection of PC in general practice, using the STHLM3 model with superior specificity and sensitivity for clinically significant PC, combined with multiparametric magnetic resonance imaging (mpMRI) of the prostate and MR guided biopsy.

Detailed Description

While early stage PC can be cured by surgery or radiation therapy, advanced PC is incurable and associated with high morbidity and mortality. Early detection is critical to save lives, but many newly diagnosed PCs are in reality non-aggressive and will not affect the patient's life or health, even if left untreated. There is an urgent need to replace current clinical practice with a more accurate diagnostic approach that can ensure early detection of aggressive PC while curable, reduce unnecessary prostate biopsies incl. risk of sepsis and reduce overdiagnosis/-treatment of indolent PC. New molecular biomarkers applied in general practice, serving as a pre-selection test for follow-up, and accurate and patient-friendly MR-imaging and MR-targeted biopsy at the hospital may help to solve these problems. In this study the investigators will assess the clinical utility of combining genetic risk testing and plasma protein markers (STHLM3 test) in general practice with mpMRI and MR-guided in bore biopsy (MRGB) for early PC detection in a biopsy naïve population.

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
December 31, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
Aarhus University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • aged 50-69 years
  • no previous pelvic cancer
  • no previous prostate biopsy
  • no previous elevated PSA results
  • informed consent from the participant

Exclusion Criteria

  • palpable prostatae tumor by digital rectal examination
  • previously diagnosed with/or treated for an urogenital cancer disease
  • contraindications to 3 T MRI
  • known severe renal impairment with estimated glomerular filtration rate \<30 ml / min

Outcomes

Primary Outcomes

Proportion of PC suspicious lesions detected by mpMRI based on the STHLM3 test vs. the prostate specific antigen test.

Time Frame: 24 months

Evaluation of the proportion of patients identified with PC suspicious lesions at mpMRI based on the STHLM3 vs. the prostate specific antigen test.

Secondary Outcomes

  • Proportion of PC diagnoses detected in the study population based on the STHLM3 test vs. the prostate specific antigen test.(24 months)
  • Compare results from clinical study with current clinical practice.(24 months)

Study Sites (1)

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