Clinical Trials Directory

Trials / Completed

CompletedNCT02380027

PRostate Evaluation for Clinically Important Disease: Sampling Using Image-guidance Or Not?

A Randomized Control Trial of Magnetic Resonance Imaging-targeted Biopsy Compared to Standard Trans-rectal Ultrasound Guided Biopsy for the Diagnosis of Prostate Cancer in Men Without Prior Biopsy

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
500 (actual)
Sponsor
University College, London · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

This evaluates the detection rates of prostate cancer by MRI-targeted prostate biopsy compared to standard 12-core trans-rectal ultrasound guided (TRUS) prostate biopsy. Each participant will be randomly allocated to one of the biopsy tests. We hypothesise that MRI-targeted biopsy will detect no fewer clinically significant cancers than TRUS biopsy but will detect fewer clinically insignificant prostate cancers than TRUS biopsy.

Detailed description

The classical pathway for the diagnosis of prostate cancer is trans-rectal ultrasound guided (TRUS) biopsy of the prostate following a raised PSA. This is currently the mainstay for prostate cancer diagnosis in the majority of centres. It has many advantages and can be performed routinely under local anaesthetic in an outpatient setting. However it does have some limitations, including the over-diagnosis of insignificant cancer and the under-diagnosis of significant cancer. An alternative pathway for the diagnosis of prostate cancer in men with raised prostate specific antigen (PSA) is to perform a multi-parametric MRI to localize cancer and to use this information to influence conduct of a subsequent biopsy, known as an MRI-targeted biopsy. MRI-targeted biopsy has been shown in preliminary studies to detect a similar amount of clinically significant cancer to TRUS-biopsy but may have several advantages, for example in reducing the number of men who require biopsy. This randomized controlled trial aims to assess the detection rate of clinically significant and clinically insignificant cancer of MRI-targeted biopsy compared to standard 12-core TRUS biopsy in men referred with clinical suspicion of prostate cancer who have had no prior prostate biopsy. A 'clinically insignificant cancer' is cancer which is unlikely to progress or affect a man's life expectancy and therefore does not warrant treatment. However when diagnosed with insignificant cancer a large proportion of patients request treatment in case a more significant cancer is present. A prostate cancer detection pathway that finds significant cancers while avoiding the diagnosis of insignificant cancer is a major unmet need. The potential implications of this trial include: * A redefining of the prostate cancer diagnostic pathway * A reduction in the number of patients undergoing prostate biopsy * A reduction in the number of biopsy cores taken per patient * A reduction in biopsy-related sepsis, pain and other side effects * A reduction in the over-diagnosis of clinically insignificant prostate cancer * A reduction of the economic burden of diagnosing and treating prostate cancer

Conditions

Interventions

TypeNameDescription
DEVICEMRIThis will be a multi-parametric MRI of the prostate
PROCEDUREMRI-targeted biopsyThis will be a biopsy targeted to suspicious areas on the MRI
PROCEDURETRUS-biopsyThis will be a standard 12 core trans-rectal prostate biopsy

Timeline

Start date
2016-01-01
Primary completion
2017-12-31
Completion
2017-12-31
First posted
2015-03-05
Last updated
2018-05-01

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02380027. Inclusion in this directory is not an endorsement.