MRI in Diagnosing Prostate Cancer
Primary Purpose
Prostate Cancer
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
biologic sample preservation procedure
laboratory biomarker analysis
study of socioeconomic and demographic variables
diffusion-weighted magnetic resonance imaging
dynamic contrast-enhanced magnetic resonance imaging
multiparametric magnetic resonance imaging
quality-of-life assessment
transperineal prostate biopsy
transrectal prostate biopsy
ultrasound-guided prostate biopsy
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostate Cancer focused on measuring stage I prostate cancer, stage IIA prostate cancer, stage IIB prostate cancer
Eligibility Criteria
DISEASE CHARACTERISTICS:
- Men at risk of prostate cancer who have been advised to have a prostate biopsy
- Suspected stage ≤ T2 on rectal examination (organ confined)
- Serum PSA ≤ 15 ng/mL within the past 3 months
PATIENT CHARACTERISTICS:
- Fit for general/spinal anesthesia
- Fit to undergo all protocol procedures including a transrectal ultrasound
- No evidence of a urinary tract infection or history of acute prostatitis within the past 3 months
- No contraindication to MRI (e.g., claustrophobia, pacemaker, or estimated GFR ≤ 50)
- No other medical condition precluding procedures described in the protocol
PRIOR CONCURRENT THERAPY:
- No prior prostate biopsy, prostate surgery, or treatment for prostate cancer (interventions for benign prostatic hyperplasia/bladder outflow obstruction are acceptable)
- No prior hip replacement surgery
Sites / Locations
Outcomes
Primary Outcome Measures
Safety of multiparametric magnetic resonance imaging (MP-MRI)
Recruitment
Proportion of men who could safely avoid biopsy as determined by specificity and negative predictive values
Proportion of men correctly identified by MP-MRI to have clinically significant prostate cancer as determined by sensitivity and positive predictive values
Secondary Outcome Measures
Proportion of men who could safely avoid biopsy
Proportion of men testing positive on MP-MRI
Performance characteristics of TRUS versus template prostate mapping (TPM)
Evaluation of the optimal combination of MP-MRI functional parameters
Intra-observer variability in the reporting of MP-MRI
Evaluation of socio-demographic, clinical, imaging and radiological variables in relation to the detection of clinically significant prostate cancer
Health-related quality of life using the EQ-5D questionnaire
Resource use and costs for further economic evaluation
Translational research
Full Information
NCT ID
NCT01292291
First Posted
February 8, 2011
Last Updated
August 6, 2013
Sponsor
University College London Hospitals
1. Study Identification
Unique Protocol Identification Number
NCT01292291
Brief Title
MRI in Diagnosing Prostate Cancer
Official Title
PROMIS - Prostate MRI Imaging Study - Evaluation of Multi-Parametric Magnetic Resonance Imaging in the Diagnosis and Characterization of Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
September 2011
Overall Recruitment Status
Unknown status
Study Start Date
April 2011 (undefined)
Primary Completion Date
April 2013 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
University College London Hospitals
4. Oversight
5. Study Description
Brief Summary
RATIONALE: Diagnostic procedures, such as magnetic resonance imaging (MRI), may help find prostate cancer and learn the extent of disease.
PURPOSE: This clinical trial is studying the safety of MRI and to see how well it works in diagnosing prostate cancer.
Detailed Description
OBJECTIVES:
To determine the ability of multiparametric magnetic resonance imaging (MP-MRI) to identify men who can safely avoid unnecessary biopsy.
To assess the ability of the MP-MRI-based diagnostic pathway to improve the rate of detection of clinically significant cancer as compared to transrectal ultrasound (TRUS) biopsy.
To estimate the cost-effectiveness of an MP-MRI based diagnostic pathway.
OUTLINE: This is a multicenter study.
Patients undergo multiparametric magnetic resonance imaging (MRI) (T2-weighted imaging, diffusion-weighted MRI, and dynamic contrast-enhanced MRI) followed by template prostate mapping and transrectal ultrasound biopsy.
Some patients may undergo blood, urine, and tissue sample collection periodically for biomarker studies. Samples are banked for future research analysis.
Patients complete a quality-of-life questionnaire (EQ-5D) at baseline, during, and after completion of study. An economic analysis will be performed for cost-effectiveness.
After completion of study intervention, patients are followed up periodically.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
stage I prostate cancer, stage IIA prostate cancer, stage IIB prostate cancer
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Enrollment
714 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Other
Intervention Name(s)
biologic sample preservation procedure
Intervention Type
Other
Intervention Name(s)
laboratory biomarker analysis
Intervention Type
Other
Intervention Name(s)
study of socioeconomic and demographic variables
Intervention Type
Procedure
Intervention Name(s)
diffusion-weighted magnetic resonance imaging
Intervention Type
Procedure
Intervention Name(s)
dynamic contrast-enhanced magnetic resonance imaging
Intervention Type
Procedure
Intervention Name(s)
multiparametric magnetic resonance imaging
Intervention Type
Procedure
Intervention Name(s)
quality-of-life assessment
Intervention Type
Procedure
Intervention Name(s)
transperineal prostate biopsy
Intervention Type
Procedure
Intervention Name(s)
transrectal prostate biopsy
Intervention Type
Procedure
Intervention Name(s)
ultrasound-guided prostate biopsy
Primary Outcome Measure Information:
Title
Safety of multiparametric magnetic resonance imaging (MP-MRI)
Title
Recruitment
Title
Proportion of men who could safely avoid biopsy as determined by specificity and negative predictive values
Title
Proportion of men correctly identified by MP-MRI to have clinically significant prostate cancer as determined by sensitivity and positive predictive values
Secondary Outcome Measure Information:
Title
Proportion of men who could safely avoid biopsy
Title
Proportion of men testing positive on MP-MRI
Title
Performance characteristics of TRUS versus template prostate mapping (TPM)
Title
Evaluation of the optimal combination of MP-MRI functional parameters
Title
Intra-observer variability in the reporting of MP-MRI
Title
Evaluation of socio-demographic, clinical, imaging and radiological variables in relation to the detection of clinically significant prostate cancer
Title
Health-related quality of life using the EQ-5D questionnaire
Title
Resource use and costs for further economic evaluation
Title
Translational research
10. Eligibility
Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS:
Men at risk of prostate cancer who have been advised to have a prostate biopsy
Suspected stage ≤ T2 on rectal examination (organ confined)
Serum PSA ≤ 15 ng/mL within the past 3 months
PATIENT CHARACTERISTICS:
Fit for general/spinal anesthesia
Fit to undergo all protocol procedures including a transrectal ultrasound
No evidence of a urinary tract infection or history of acute prostatitis within the past 3 months
No contraindication to MRI (e.g., claustrophobia, pacemaker, or estimated GFR ≤ 50)
No other medical condition precluding procedures described in the protocol
PRIOR CONCURRENT THERAPY:
No prior prostate biopsy, prostate surgery, or treatment for prostate cancer (interventions for benign prostatic hyperplasia/bladder outflow obstruction are acceptable)
No prior hip replacement surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Emberton, MD, FRCS, MBBS
Organizational Affiliation
University College London Hospitals
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
30040065
Citation
Brown LC, Ahmed HU, Faria R, El-Shater Bosaily A, Gabe R, Kaplan RS, Parmar M, Collaco-Moraes Y, Ward K, Hindley RG, Freeman A, Kirkham A, Oldroyd R, Parker C, Bott S, Burns-Cox N, Dudderidge T, Ghei M, Henderson A, Persad R, Rosario DJ, Shergill I, Winkler M, Soares M, Spackman E, Sculpher M, Emberton M. Multiparametric MRI to improve detection of prostate cancer compared with transrectal ultrasound-guided prostate biopsy alone: the PROMIS study. Health Technol Assess. 2018 Jul;22(39):1-176. doi: 10.3310/hta22390.
Results Reference
derived
PubMed Identifier
28110982
Citation
Ahmed HU, El-Shater Bosaily A, Brown LC, Gabe R, Kaplan R, Parmar MK, Collaco-Moraes Y, Ward K, Hindley RG, Freeman A, Kirkham AP, Oldroyd R, Parker C, Emberton M; PROMIS study group. Diagnostic accuracy of multi-parametric MRI and TRUS biopsy in prostate cancer (PROMIS): a paired validating confirmatory study. Lancet. 2017 Feb 25;389(10071):815-822. doi: 10.1016/S0140-6736(16)32401-1. Epub 2017 Jan 20.
Results Reference
derived
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MRI in Diagnosing Prostate Cancer
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