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

Primary Purpose

Prostate Neoplasm

Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
MRI
MRI-targeted biopsy
TRUS-biopsy
Sponsored by
University College, London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Neoplasm focused on measuring Prostate biopsy, MRI, transrectal, Detection

Eligibility Criteria

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

Inclusion Criteria:

  1. Men at least 18 years of age referred with clinical suspicion of prostate cancer who have been advised to have a prostate biopsy
  2. Serum PSA ≤ 20ng/ml within the previous 3 months
  3. Suspected stage ≤ T2 on rectal examination (organ-confined prostate cancer) within the previous 3 months
  4. Fit to undergo all procedures listed in protocol
  5. Able to provide written informed consent

Exclusion Criteria:

  1. Prior prostate biopsy
  2. Prior treatment for prostate cancer
  3. Contraindication to MRI (e.g. claustrophobia, pacemaker, estimated glomerular filtration rate ≤ 50mls/min)
  4. Contraindication to prostate biopsy
  5. Men in whom artifact would reduce the quality of the MRI
  6. Previous hip replacement surgery, metallic hip replacement or extensive pelvic orthopaedic metal work
  7. Unfit to undergo any procedures listed in protocol

Sites / Locations

  • University College Hospitals

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

MRI-arm

TRUS-biopsy arm

Arm Description

Men in this arm will undergo multi-parametric MRI. In the presence of a suspicious area, a man will undergo MRI-targeted biopsy with cores targeted to the suspicious lesion. In the absence of a suspicious area, no biopsy will be taken.

Men in this arm undergo standard 12-core trans-rectal ultrasound guided prostate biopsy

Outcomes

Primary Outcome Measures

Proportion of men with clinically significant detected

Secondary Outcome Measures

Proportion of men in MRI arm who avoid biopsy
Proportion of men with MRI score 3, 4 or 5 who have no clinically significant cancer detected
Proportion of men who go on to definitive treatment for prostate cancer
Definitive treatment can be localised (e.g. radical prostatectomy, radiotherapy, brachytherapy) or systemic (hormone therapy, chemotherapy)
Cancer core length of the most involved biopsy core (maximum cancer core length)
Cancer core length in mm
Proportion of men with post-biopsy adverse events
EQ-5D-5L Quality of Life scores
EQ-5D gives a measure of health-related quality of life. The descriptive system gives a weighted index score from 0-1 where 1 is perfect health and 0 is the worst health possible. The visual analogue score is a measure of overall self-rated health status where 100 is the best imaginable health state and 0 is the worst imaginable health state.
Proportion of men undergoing Radical prostatectomy who have Gleason grade upgrading
Cost per diagnosis of cancer
Proportion of men with clinically insignificant detected

Full Information

First Posted
February 23, 2015
Last Updated
April 30, 2018
Sponsor
University College, London
Collaborators
National Institute for Health Research, United Kingdom, University Hospital, Lille, Radboud University Medical Center, London North West Healthcare NHS Trust, Royal Free Hospital NHS Foundation Trust, Sunnybrook Health Sciences Centre, University College London Hospitals, University Ghent, Helsinki University Central Hospital, Jewish General Hospital, University of Roma La Sapienza, Göteborg University, Erasmus Medical Center, Hunter Holmes Mcguire Veteran Affairs Medical Center, University Hospital Heidelberg, University Hospital, Aachen, Hampshire Hospitals NHS Foundation Trust, Princess Alexandra Hospital NHS Trust, San Raffaele University Hospital, Italy, M.D. Anderson Cancer Center, University Hospital Southampton NHS Foundation Trust, University of Oulu, The Whittington Hospital NHS Trust, University Hospital of Cologne, Mayo Clinic, Centro de Urologia Argentina, Weill Medical College of Cornell University, University of Chicago, University Hospital, Bordeaux
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1. Study Identification

Unique Protocol Identification Number
NCT02380027
Brief Title
PRostate Evaluation for Clinically Important Disease: Sampling Using Image-guidance Or Not?
Acronym
PRECISION
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
January 2016 (undefined)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
December 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University College, London
Collaborators
National Institute for Health Research, United Kingdom, University Hospital, Lille, Radboud University Medical Center, London North West Healthcare NHS Trust, Royal Free Hospital NHS Foundation Trust, Sunnybrook Health Sciences Centre, University College London Hospitals, University Ghent, Helsinki University Central Hospital, Jewish General Hospital, University of Roma La Sapienza, Göteborg University, Erasmus Medical Center, Hunter Holmes Mcguire Veteran Affairs Medical Center, University Hospital Heidelberg, University Hospital, Aachen, Hampshire Hospitals NHS Foundation Trust, Princess Alexandra Hospital NHS Trust, San Raffaele University Hospital, Italy, M.D. Anderson Cancer Center, University Hospital Southampton NHS Foundation Trust, University of Oulu, The Whittington Hospital NHS Trust, University Hospital of Cologne, Mayo Clinic, Centro de Urologia Argentina, Weill Medical College of Cornell University, University of Chicago, University Hospital, Bordeaux

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Neoplasm
Keywords
Prostate biopsy, MRI, transrectal, Detection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
500 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MRI-arm
Arm Type
Experimental
Arm Description
Men in this arm will undergo multi-parametric MRI. In the presence of a suspicious area, a man will undergo MRI-targeted biopsy with cores targeted to the suspicious lesion. In the absence of a suspicious area, no biopsy will be taken.
Arm Title
TRUS-biopsy arm
Arm Type
Active Comparator
Arm Description
Men in this arm undergo standard 12-core trans-rectal ultrasound guided prostate biopsy
Intervention Type
Device
Intervention Name(s)
MRI
Intervention Description
This will be a multi-parametric MRI of the prostate
Intervention Type
Procedure
Intervention Name(s)
MRI-targeted biopsy
Intervention Description
This will be a biopsy targeted to suspicious areas on the MRI
Intervention Type
Procedure
Intervention Name(s)
TRUS-biopsy
Intervention Description
This will be a standard 12 core trans-rectal prostate biopsy
Primary Outcome Measure Information:
Title
Proportion of men with clinically significant detected
Time Frame
When histology results available, at an expected average of 30 days post-biopsy
Secondary Outcome Measure Information:
Title
Proportion of men in MRI arm who avoid biopsy
Time Frame
When MRI results available, at an expected average of 30 days post-MRI
Title
Proportion of men with MRI score 3, 4 or 5 who have no clinically significant cancer detected
Time Frame
When histology results available, at an expected average of 30 days post-biopsy
Title
Proportion of men who go on to definitive treatment for prostate cancer
Description
Definitive treatment can be localised (e.g. radical prostatectomy, radiotherapy, brachytherapy) or systemic (hormone therapy, chemotherapy)
Time Frame
After treatment decision, at an expected average of 30 days post-biopsy
Title
Cancer core length of the most involved biopsy core (maximum cancer core length)
Description
Cancer core length in mm
Time Frame
When histology results available, at an expected average of 30 days post-biopsy
Title
Proportion of men with post-biopsy adverse events
Time Frame
30 days post biopsy
Title
EQ-5D-5L Quality of Life scores
Description
EQ-5D gives a measure of health-related quality of life. The descriptive system gives a weighted index score from 0-1 where 1 is perfect health and 0 is the worst health possible. The visual analogue score is a measure of overall self-rated health status where 100 is the best imaginable health state and 0 is the worst imaginable health state.
Time Frame
Baseline, 24 hours post intervention and 30 days post intervention
Title
Proportion of men undergoing Radical prostatectomy who have Gleason grade upgrading
Time Frame
An expected average of 90 days post-biopsy
Title
Cost per diagnosis of cancer
Time Frame
30 days post-biopy
Title
Proportion of men with clinically insignificant detected
Time Frame
When histology results available, at an expected average of 30 days post-biopsy

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men at least 18 years of age referred with clinical suspicion of prostate cancer who have been advised to have a prostate biopsy Serum PSA ≤ 20ng/ml within the previous 3 months Suspected stage ≤ T2 on rectal examination (organ-confined prostate cancer) within the previous 3 months Fit to undergo all procedures listed in protocol Able to provide written informed consent Exclusion Criteria: Prior prostate biopsy Prior treatment for prostate cancer Contraindication to MRI (e.g. claustrophobia, pacemaker, estimated glomerular filtration rate ≤ 50mls/min) Contraindication to prostate biopsy Men in whom artifact would reduce the quality of the MRI Previous hip replacement surgery, metallic hip replacement or extensive pelvic orthopaedic metal work Unfit to undergo any procedures listed in protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Caroline Moore, MD FRCS
Organizational Affiliation
University College Hospital London and University College London
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mark Emberton, MD FRCS
Organizational Affiliation
University College Hospital London and University College London
Official's Role
Study Chair
Facility Information:
Facility Name
University College Hospitals
City
London
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
29552975
Citation
Kasivisvanathan V, Rannikko AS, Borghi M, Panebianco V, Mynderse LA, Vaarala MH, Briganti A, Budaus L, Hellawell G, Hindley RG, Roobol MJ, Eggener S, Ghei M, Villers A, Bladou F, Villeirs GM, Virdi J, Boxler S, Robert G, Singh PB, Venderink W, Hadaschik BA, Ruffion A, Hu JC, Margolis D, Crouzet S, Klotz L, Taneja SS, Pinto P, Gill I, Allen C, Giganti F, Freeman A, Morris S, Punwani S, Williams NR, Brew-Graves C, Deeks J, Takwoingi Y, Emberton M, Moore CM; PRECISION Study Group Collaborators. MRI-Targeted or Standard Biopsy for Prostate-Cancer Diagnosis. N Engl J Med. 2018 May 10;378(19):1767-1777. doi: 10.1056/NEJMoa1801993. Epub 2018 Mar 18.
Results Reference
derived
PubMed Identifier
29025845
Citation
Kasivisvanathan V, Jichi F, Klotz L, Villers A, Taneja SS, Punwani S, Freeman A, Emberton M, Moore CM. A multicentre randomised controlled trial assessing whether MRI-targeted biopsy is non-inferior to standard transrectal ultrasound guided biopsy for the diagnosis of clinically significant prostate cancer in men without prior biopsy: a study protocol. BMJ Open. 2017 Oct 12;7(10):e017863. doi: 10.1136/bmjopen-2017-017863.
Results Reference
derived

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

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