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Clinical Trials/NCT01492270
NCT01492270
Unknown
Not Applicable

PICTURE - Prostate Imaging (Multi-parametric MRI and Prostate HistoScanning™) Compared to Transperineal Ultrasound Guided Biopsy for Significant Prostate Cancer Risk Evaluation.

University College London Hospitals1 site in 1 country126 target enrollmentDecember 2011
ConditionsProstate Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
University College London Hospitals
Enrollment
126
Locations
1
Primary Endpoint
Number of men who could avoid repeat biopsy as determined by the Negative predictive value and specificity of mp-MRI for Clinically significant disease.
Last Updated
14 years ago

Overview

Brief Summary

The incidence of prostate cancer is rising however the number of deaths from prostate cancer is stable. Meaning the investigators are diagnosing many men with prostate cancer that will not impact on their life. The rise in incidence is mainly due to increased use of the blood test Prostate Specific Antigen (PSA), as a screening test.

Currently men suspected of having prostate cancer, identified by a raised PSA undergo trans-rectal ultrasound guided prostate biopsy (TRUS biopsy). Many men have this test unnecessarily, only 1/3 being diagnosed with prostate cancer. TRUS biopsy is problematic as it is random and performed blind-the operator does not know where the cancer is. Thus many low-risk cancers that do not need treating are diagnosed and many high risk cancers are missed or incorrectly classified. So, men with a negative biopsy or those with low risk disease are usually advised to undergo another TRUS biopsy.

An imaging test is needed that could help men and their doctors decide whether the biopsy is a true reflection of what is inside his prostate.

The investigators will test the role of two imaging tests. The first, multi-parametric magnetic resonance imaging (mp-MRI) uses magnetic signals from the body to form images. The second, Prostate HistoScanning™ (PHS) uses sound-waves. The investigators will compare the results of these tests with a detailed biopsy map-transperineal template prostate mapping biopsy (which is currently the best way to find out what is in the prostate but requires multiple biopsies to be taken under general anaesthetic. Eligible men will have undergone one or more TRUS biopsies and who have been advised to have further tests on as part of standard of care. They will be recruited from UCLH referral letters and clinics.

The investigators aim is to see if either of these tests can confidently rule out the presence of clinically important disease.

Registry
clinicaltrials.gov
Start Date
December 2011
End Date
July 2013
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
University College London Hospitals
Responsible Party
Principal Investigator
Principal Investigator

Professor Mark Emberton

Professor of Interventional Oncology

University College London Hospitals

Eligibility Criteria

Inclusion Criteria

  • Men who have undergone prior trans-rectal biopsies.
  • Men undergoing further evaluation of their prostate and who are seeking characterisation using Transperineal Template Prostate Mapping Biopsy.

Exclusion Criteria

  • Previous history of prostate cancer treatment
  • Men unable to have MRI scan, or in whom artefact would reduce quality of MRI.
  • Men unable to have general or regional anaesthesia
  • Men unable to give informed consent

Outcomes

Primary Outcomes

Number of men who could avoid repeat biopsy as determined by the Negative predictive value and specificity of mp-MRI for Clinically significant disease.

Time Frame: 18 months

Performance characteristics of mp-MRI for ruling out CLINICALLY SIGNIFICANT prostate cancer as determined by negative predictive value and specificity

Number of men who could avoid repeat biopsy as determined by the negative predictive value and specificity of Prostate HistoScanning for Clinically significant disease.

Time Frame: 18 months

Performance characteristics of Prostate HistoScanning for ruling out CLINICALLY SIGNIFICANT prostate cancer as determined by negative predictive value and specificity

Secondary Outcomes

  • Proportion of men correctly identified as having no cancer on Imaging (mp-MRI and Prostate HistoScanning)(18 months)
  • Number of men correctly identified by Imaging (mp-MRI and Prostate HistoScanning) to have CLINICALLY SIGNIFICANT disease(18 months)
  • Test- retest reproducibility of Prostate HistoScanning™.(18 months)
  • Proportion of patients with correct disease risk stratification using MRI/US guided biopsies as determined by sensitivity and specificity(18 months)
  • Number of patients with bothersome Lower Urinary tract symptoms following Transperineal Template Mapping biopsy(18 months)
  • Number of patients with worsened erectile function compared to baseline following Transperineal Template Mapping biopsy(18 months)

Study Sites (1)

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