search
Back to results

Imaging for Significant Prostate Cancer Risk Evaluation (PICTURE)

Primary Purpose

Prostate Cancer

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Prostate HistoScanning
Multi-parametric MRI
Transperineal prostate mapping biopsy
Image guided biopsies
Sponsored by
University College London Hospitals
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Cancer focused on measuring Prostate Cancer, Multi parametric MRI, Prostate HistoScanning, Transperineal prostate mapping biopsy

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

Sites / Locations

  • University College London HospitalsRecruiting

Outcomes

Primary Outcome Measures

Number of men who could avoid repeat biopsy as determined by the Negative predictive value and specificity of mp-MRI for Clinically significant disease.
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.
Performance characteristics of Prostate HistoScanning for ruling out CLINICALLY SIGNIFICANT prostate cancer as determined by negative predictive value and specificity

Secondary Outcome Measures

Proportion of men correctly identified as having no cancer on Imaging (mp-MRI and Prostate HistoScanning)
Negative predictive value of Imaging compared to Transperineal template Mapping prostate biopsy.
Number of men correctly identified by Imaging (mp-MRI and Prostate HistoScanning) to have CLINICALLY SIGNIFICANT disease
Number of men correctly identified by each test to have clinically significant disease as detected by Transperineal Template Mapping Biopsy
Test- retest reproducibility of Prostate HistoScanning™.
The reproducibility of Prostate HistoScanning will be assessed by looking at the predicted cancer volume and location of the HistoScanning investigation at two time points.
Proportion of patients with correct disease risk stratification using MRI/US guided biopsies as determined by sensitivity and specificity
Performance characteristics of MRI/US registration targeted biopsies compared to i) systematic biopsies and ii) cognitive targeted biopsies in prostate cancer risk stratification as determined by sensitivity and specificity
Number of patients with bothersome Lower Urinary tract symptoms following Transperineal Template Mapping biopsy
Assessment of alterations in Lower Urinary tract function following Transperineal Template Mapping Biopsy IPSS, IPSS-QoL, Continence Function Questionnaire.
Number of patients with worsened erectile function compared to baseline following Transperineal Template Mapping biopsy
Assesment of erectile function compared to baseline will be made using questionnairres. IIEF

Full Information

First Posted
December 6, 2011
Last Updated
December 28, 2011
Sponsor
University College London Hospitals
Collaborators
Advanced Medical Diagnostics s.a.
search

1. Study Identification

Unique Protocol Identification Number
NCT01492270
Brief Title
Imaging for Significant Prostate Cancer Risk Evaluation
Acronym
PICTURE
Official Title
PICTURE - Prostate Imaging (Multi-parametric MRI and Prostate HistoScanning™) Compared to Transperineal Ultrasound Guided Biopsy for Significant Prostate Cancer Risk Evaluation.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2011
Overall Recruitment Status
Unknown status
Study Start Date
December 2011 (undefined)
Primary Completion Date
July 2013 (Anticipated)
Study Completion Date
July 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University College London Hospitals
Collaborators
Advanced Medical Diagnostics s.a.

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate Cancer, Multi parametric MRI, Prostate HistoScanning, Transperineal prostate mapping biopsy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
126 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Prostate HistoScanning
Intervention Description
Advanced Ultrasound assessment of the prostate
Intervention Type
Procedure
Intervention Name(s)
Multi-parametric MRI
Intervention Description
Multi-sequence Magnetic resonance imaging of the prostate
Intervention Type
Procedure
Intervention Name(s)
Transperineal prostate mapping biopsy
Intervention Description
Needle biopsy of the perineum via the transperineal route at 5mm intervals guided by the use of ultrasound.
Intervention Type
Procedure
Intervention Name(s)
Image guided biopsies
Other Intervention Name(s)
Targeted Biopsy
Intervention Description
Biopsies targeted to lesions seen at a) Prostate HistoScanning and b) mp-MRI. In men with an MRI lesion further MRI/US registration biopsies will be obtained
Primary Outcome Measure Information:
Title
Number of men who could avoid repeat biopsy as determined by the Negative predictive value and specificity of mp-MRI for Clinically significant disease.
Description
Performance characteristics of mp-MRI for ruling out CLINICALLY SIGNIFICANT prostate cancer as determined by negative predictive value and specificity
Time Frame
18 months
Title
Number of men who could avoid repeat biopsy as determined by the negative predictive value and specificity of Prostate HistoScanning for Clinically significant disease.
Description
Performance characteristics of Prostate HistoScanning for ruling out CLINICALLY SIGNIFICANT prostate cancer as determined by negative predictive value and specificity
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Proportion of men correctly identified as having no cancer on Imaging (mp-MRI and Prostate HistoScanning)
Description
Negative predictive value of Imaging compared to Transperineal template Mapping prostate biopsy.
Time Frame
18 months
Title
Number of men correctly identified by Imaging (mp-MRI and Prostate HistoScanning) to have CLINICALLY SIGNIFICANT disease
Description
Number of men correctly identified by each test to have clinically significant disease as detected by Transperineal Template Mapping Biopsy
Time Frame
18 months
Title
Test- retest reproducibility of Prostate HistoScanning™.
Description
The reproducibility of Prostate HistoScanning will be assessed by looking at the predicted cancer volume and location of the HistoScanning investigation at two time points.
Time Frame
18 months
Title
Proportion of patients with correct disease risk stratification using MRI/US guided biopsies as determined by sensitivity and specificity
Description
Performance characteristics of MRI/US registration targeted biopsies compared to i) systematic biopsies and ii) cognitive targeted biopsies in prostate cancer risk stratification as determined by sensitivity and specificity
Time Frame
18 months
Title
Number of patients with bothersome Lower Urinary tract symptoms following Transperineal Template Mapping biopsy
Description
Assessment of alterations in Lower Urinary tract function following Transperineal Template Mapping Biopsy IPSS, IPSS-QoL, Continence Function Questionnaire.
Time Frame
18 months
Title
Number of patients with worsened erectile function compared to baseline following Transperineal Template Mapping biopsy
Description
Assesment of erectile function compared to baseline will be made using questionnairres. IIEF
Time Frame
18 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lucy AM Simmons, MBBS
Phone
0044 (0) 207 679 9092
Email
lucy.simmons@uclh.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Emberton, MBBS,MD,FRCS
Organizational Affiliation
University College London Hospitals
Official's Role
Principal Investigator
Facility Information:
Facility Name
University College London Hospitals
City
London
ZIP/Postal Code
NW1 2PG
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lucy AM Simmons, MBBS, MRCS
Phone
0044 203 447 9194
Email
lucy.simmons@uclh.nhs.uk
First Name & Middle Initial & Last Name & Degree
Hashim Uddin Ahmed, MBBS, MRCS
Phone
0044 203 447 9194
First Name & Middle Initial & Last Name & Degree
Hashim Uddin Ahmed, MBBS, MRCS
First Name & Middle Initial & Last Name & Degree
Caroline M Moore, MBBS,MD,FRCS

12. IPD Sharing Statement

Citations:
PubMed Identifier
30279583
Citation
Simmons LAM, Kanthabalan A, Arya M, Briggs T, Charman SC, Freeman A, Gelister J, Jameson C, McCartan N, Moore CM, van der Muelen J, Emberton M, Ahmed HU. Prostate Imaging Compared to Transperineal Ultrasound-guided biopsy for significant prostate cancer Risk Evaluation (PICTURE): a prospective cohort validating study assessing Prostate HistoScanning. Prostate Cancer Prostatic Dis. 2019 May;22(2):261-267. doi: 10.1038/s41391-018-0094-1. Epub 2018 Oct 2.
Results Reference
derived
PubMed Identifier
30017964
Citation
Simmons LAM, Kanthabalan A, Arya M, Briggs T, Barratt D, Charman SC, Freeman A, Hawkes D, Hu Y, Jameson C, McCartan N, Moore CM, Punwani S, van der Muelen J, Emberton M, Ahmed HU. Accuracy of Transperineal Targeted Prostate Biopsies, Visual Estimation and Image Fusion in Men Needing Repeat Biopsy in the PICTURE Trial. J Urol. 2018 Dec;200(6):1227-1234. doi: 10.1016/j.juro.2018.07.001. Epub 2018 Jul 11.
Results Reference
derived
PubMed Identifier
29940251
Citation
Miah S, Eldred-Evans D, Simmons LAM, Shah TT, Kanthabalan A, Arya M, Winkler M, McCartan N, Freeman A, Punwani S, Moore CM, Emberton M, Ahmed HU. Patient Reported Outcome Measures for Transperineal Template Prostate Mapping Biopsies in the PICTURE Study. J Urol. 2018 Dec;200(6):1235-1240. doi: 10.1016/j.juro.2018.06.033. Epub 2018 Jun 27.
Results Reference
derived

Learn more about this trial

Imaging for Significant Prostate Cancer Risk Evaluation

We'll reach out to this number within 24 hrs