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ReIMAGINE Prostate Cancer Screening

Primary Purpose

Prostate Cancer Screening, Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Magnetic Resonance Imaging (MRI)
Prostate-specific antigen (PSA) test
Sponsored by
University College, London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Prostate Cancer Screening focused on measuring Prostate Cancer, MRI, PSA

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Men aged 50-75
  2. No prior prostate cancer diagnosis / treatment
  3. Willing and able to provide written informed consent.

Exclusion Criteria:

  1. Contraindication for MRI scanning (as assessed by the MRI safety questionnaire of the PET/MRI department) which includes but is not limited to: Intracranial aneurysm clips or other metallic objects; Intra-orbital metal fragments that have not been removed; Pacemakers or other implanted cardiac rhythm management devices and non-MRI compatible heart valves; Inner ear implants; and History of claustrophobia
  2. Men who require assisted living e.g. care home living
  3. Dementia or other neurological condition meaning participant lacks the capacity to consent.

Sites / Locations

  • University College London Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Total cohort

Arm Description

The study will consist of one group, one arm, all receiving the same screening procedures.

Outcomes

Primary Outcome Measures

The acceptance rate of an invitation for a screening prostate MRI in men who have not had a prostate cancer diagnosis
Proportion of men who accept the invitation for prostate screening
The prevalence of MRI defined suspicious lesions in men accepting a screening invitation
The prevalence of MRI defined suspicious lesions in men accepting a screening invitation
Presence of cancer in men who have biopsy as a result of their MRI findings
The prevalence of men being diagnosed with prostate cancer who have biopsy as a result of their MRI findings

Secondary Outcome Measures

The proportion of men ineligible due to prior prostate cancer diagnosis
The proportion of men ineligible due to prior prostate cancer diagnosis
The proportion of men who screen negative on MRI
The proportion of men who screen negative on MRI
The proportion of men who screen negative on PSA density
The proportion of men who screen negative on PSA density
The proportion of men who screen positive on MRI alone
The proportion of men who screen positive on MRI alone
The proportion of men who screen positive on PSA density alone
The proportion of men who screen positive on PSA density alone

Full Information

First Posted
August 15, 2019
Last Updated
October 8, 2021
Sponsor
University College, London
Collaborators
Medical Research Council, Cancer Research UK, Imperial College London, King's College London
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1. Study Identification

Unique Protocol Identification Number
NCT04063566
Brief Title
ReIMAGINE Prostate Cancer Screening
Official Title
ReIMAGINE Prostate Cancer Screening - Inviting Men for Prostate Cancer Screening Using MRI
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
October 21, 2019 (Actual)
Primary Completion Date
July 30, 2021 (Actual)
Study Completion Date
September 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University College, London
Collaborators
Medical Research Council, Cancer Research UK, Imperial College London, King's College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Single site study to assess the feasibility of prostate cancer screening using an invitation for a prostate MRI scan via GP practices. This feasibility study will assess the acceptability of an MRI as a prostate cancer screening assessment and assess the prevalence of MRI defined suspicious lesions and cancer in men across a spectrum of PSA results.
Detailed Description
ReIMAGINE Prostate cancer screening is a single site screening study to assess the feasibility of MRI as a screening tool for prostate care and determine the prevalence of MRI defined suspicious lesions and cancer in men across a spectrum of PSA results. Men with no previous prostate cancer diagnosis, but deemed suitable based on age will be identified through general practitioner (GP) practices who will act as participant identification centres (PIC's). Potential participants will be identified through screening of existing patient databases at multiple London GP surgeries participating in the study, and randomly selected for invitation. The ReIMAGINE study team will link with London cancer networks and Noclor research support (https://www.noclor.nhs.uk/) who will make first contact with potentially eligible men. A personalised invitation letter from each man's own GP will be sent to him. Invitation letters will be sent in batches so to limit the time between the invitation and their study visit. Batched invitations will be prepared using an iterative process so to allow the study team to assess uptake rates and limit the gap between invitation and study visits. Invitation letters will include contact details for the ReIMAGINE study team who will coordinate bookings for research visits for all responders. All consented men will have a blood test for PSA and a screening MRI scan. This will take a maximum of 20 minutes, and will include T2, diffusion and research specific sequences. Two radiologists will report the MRI blinded to the PSA result, with a third reviewer when there is disagreement between reporters. Men in whom a suspicious lesion is seen (MRI screen positive) or who have a suspicious PSA density (>0.12ng/ml) will be recommended to have an National Health Service (NHS) referral for suspected prostate cancer as per National Institute for Health and Care Excellence (NICE) guidelines. Screen negative men will at this point exit the study. Screen positive men will be followed up to gather data from any investigations (mpMRI +/- prostate biopsy) that may occur as a result of the NHS referral. No formal visits will be required to collect this data. Participant consent will be sought to approach GP or other secondary care centre.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer Screening, Prostate Cancer
Keywords
Prostate Cancer, MRI, PSA

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single site screening study to assess the feasibility of MRI as a screening tool for prostate care and determine the prevalence of MRI defined suspicious lesions and cancer in men across a spectrum of PSA results.
Masking
None (Open Label)
Allocation
N/A
Enrollment
309 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Total cohort
Arm Type
Other
Arm Description
The study will consist of one group, one arm, all receiving the same screening procedures.
Intervention Type
Procedure
Intervention Name(s)
Magnetic Resonance Imaging (MRI)
Intervention Description
Prostate cancer screening MRI
Intervention Type
Procedure
Intervention Name(s)
Prostate-specific antigen (PSA) test
Intervention Description
Blood test for PSA levels
Primary Outcome Measure Information:
Title
The acceptance rate of an invitation for a screening prostate MRI in men who have not had a prostate cancer diagnosis
Description
Proportion of men who accept the invitation for prostate screening
Time Frame
3 years
Title
The prevalence of MRI defined suspicious lesions in men accepting a screening invitation
Description
The prevalence of MRI defined suspicious lesions in men accepting a screening invitation
Time Frame
3 years
Title
Presence of cancer in men who have biopsy as a result of their MRI findings
Description
The prevalence of men being diagnosed with prostate cancer who have biopsy as a result of their MRI findings
Time Frame
3 years
Secondary Outcome Measure Information:
Title
The proportion of men ineligible due to prior prostate cancer diagnosis
Description
The proportion of men ineligible due to prior prostate cancer diagnosis
Time Frame
3 years
Title
The proportion of men who screen negative on MRI
Description
The proportion of men who screen negative on MRI
Time Frame
3 years
Title
The proportion of men who screen negative on PSA density
Description
The proportion of men who screen negative on PSA density
Time Frame
3 years
Title
The proportion of men who screen positive on MRI alone
Description
The proportion of men who screen positive on MRI alone
Time Frame
3 years
Title
The proportion of men who screen positive on PSA density alone
Description
The proportion of men who screen positive on PSA density alone
Time Frame
3 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men aged 50-75 No prior prostate cancer diagnosis / treatment Willing and able to provide written informed consent. Exclusion Criteria: Contraindication for MRI scanning (as assessed by the MRI safety questionnaire of the PET/MRI department) which includes but is not limited to: Intracranial aneurysm clips or other metallic objects; Intra-orbital metal fragments that have not been removed; Pacemakers or other implanted cardiac rhythm management devices and non-MRI compatible heart valves; Inner ear implants; and History of claustrophobia Men who require assisted living e.g. care home living Dementia or other neurological condition meaning participant lacks the capacity to consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Caroline Moore, FRCS
Organizational Affiliation
univeristy college london
Official's Role
Principal Investigator
Facility Information:
Facility Name
University College London Hospital
City
London
ZIP/Postal Code
NW1 2PG
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34593491
Citation
Marsden T, Lomas DJ, McCartan N, Hadley J, Tuck S, Brown L, Haire A, Moss CL, Green S, Van Hemelrijck M, Coolen T, Santaolalla A, Isaac E, Brembilla G, Kopcke D, Giganti F, Sidhu H, Punwani S, Emberton M, Moore CM; ReIMAGINE Study Group. ReIMAGINE Prostate Cancer Screening Study: protocol for a single-centre feasibility study inviting men for prostate cancer screening using MRI. BMJ Open. 2021 Sep 30;11(9):e048144. doi: 10.1136/bmjopen-2020-048144.
Results Reference
derived
PubMed Identifier
34110033
Citation
Wurnschimmel C, Kachanov M, Wenzel M, Mandel P, Karakiewicz PI, Maurer T, Steuber T, Tilki D, Graefen M, Budaus L. Twenty-year trends in prostate cancer stage and grade migration in a large contemporary german radical prostatectomy cohort. Prostate. 2021 Sep;81(12):849-856. doi: 10.1002/pros.24181. Epub 2021 Jun 10.
Results Reference
derived
PubMed Identifier
33896710
Citation
Marsden T, McCartan N, Hadley J, Tuck S, Brown L, Haire AJ, Moss CL, Green S, Van Hemelrijck M, Coolen T, Santaolalla A, Isaac E, Brembilla G, Kopcke D, Giganti F, Sidhu H, Punwani S, Emberton M, Moore CM; ReIMAGINE Study Group. Update from the ReIMAGINE Prostate Cancer Screening Study NCT04063566: Inviting Men for Prostate Cancer Screening Using Magnetic Resonance Imaging. Eur Urol Focus. 2021 May;7(3):503-505. doi: 10.1016/j.euf.2021.03.027. Epub 2021 Apr 23.
Results Reference
derived

Learn more about this trial

ReIMAGINE Prostate Cancer Screening

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