Multiparametric MRI in Men With Prostate Cancer Enrolled in Active Surveillance
Primary Purpose
Prostatic Neoplasms
Status
Enrolling by invitation
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
multiparametric MRI Diagnostics
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostatic Neoplasms focused on measuring Prostate biopsy, Prostate cancer, Magnetic resonance imaging, Neoplasm staging
Eligibility Criteria
Inclusion Criteria:
- Patients with low risk localized prostate cancer enrolled in active surveillance
Exclusion Criteria:
- Metastatic prostate cancer
- No mp-MRI data present
- Prostate cancer treatment
- Known allergic reaction to Gadolinium-based MRI contrast agent
- Prostate biopsy during the last 21 days
- Impaired renal function with GFR < 30 ml / min
- pacemaker
- Magnetic metal residues in the body
- Claustrophobia
- Psychiatric disorders
- Age under 18 year
Sites / Locations
- Department of Urology, Herlev University Hospital Herlev
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Enrolled AS patients
Arm Description
Patients with prostate cancer enrolled i active surveillance protocol using PSA, digital rectal examination and conventional TRUS-biopsies
Outcomes
Primary Outcome Measures
Changes in treatment from active surveillance (observation) to active treatment based on mp-MRI results.
Patients enrolled in active surveillance will progress to active treatment if mp-MRI show previously undetected suspicious areas of significant disease. Significant cancer (measured by Gleason score and cancer core involvement on biopsies) will be confirmed by repeat biopsies of the suspicious areas. The decision to progress to active treatment is based on decision from the treating urologist.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03648359
Brief Title
Multiparametric MRI in Men With Prostate Cancer Enrolled in Active Surveillance
Official Title
Multiparametric MRI in Men With Prostate Cancer Enrolled in Active Surveillance
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Herlev Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To investigate whether multiparametric MRI (mp-MRI) in patients with low-risk prostate cancer can improve the selection of patients suitable for Active Surveillance and have a relevance in the ongoing monitoring
Detailed Description
Men with localized prostate cancer (PCa) with small tumor burden may be followed on active surveillance (AS) rather than active treatment. AS is an attempt to avoid over-treatment of PCa, which is estimated to be insignificant at the time of diagnosis, and therefore unlikely to affect patient morbidity and mortality. AS include close monitoring with PSA measurement (blood test), digital rectal exploration (DRE) and trans-rectal ultrasound-guided prostate biopsy (TRUS-bx) at regular intervals, so that active treatment can be initiated if the cancer becomes more aggressive. It is crucial that patients undergoing AS are staged correctly, to avoid underestimating more aggressive disease and patients mistakenly are enrolled into AS instead of active treatment.
Previously, a PhD study conducted at Herlev Hospital revealed that multiparametric MRI (mp-MRI) of the prostate can improve the detection and staging of PCa and may add additional information about tumor aggressiveness compared to the traditional methods DRE and TRUS-bx. Mp-MRI at the inclusion of AS may detect missed significant tumors and potential areas of higher aggressiveness than detected by the traditional biopsies. Additional targeted biopsies from these suspicious areas can then be performed with a re-evaluation of the treatment plan, if more advanced disease is identified. Conversely, mp-MRI has a high negative predicted value for significant disease and can be used to rule out significant PCa, reassuring patients and physicians to go on with AS. Mp-MRI has been used at the Urology Department, Herlev Hospital, since 2013 in the diagnosis of PCa and in the evaluation of patients undergoing AS. A retrospective study have show that mp-MRi improve the detection of missed significant PCa.
The main objective of this study is now to prospectively investigate, whether mp-MRI can improve the selection of patients suitable for Active Surveillance and have a relevance in the ongoing monitoring.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms
Keywords
Prostate biopsy, Prostate cancer, Magnetic resonance imaging, Neoplasm staging
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Enrolled AS patients
Arm Type
Other
Arm Description
Patients with prostate cancer enrolled i active surveillance protocol using PSA, digital rectal examination and conventional TRUS-biopsies
Intervention Type
Procedure
Intervention Name(s)
multiparametric MRI Diagnostics
Intervention Description
Patients with newly diagnosed prostate cancer enrolled in active surveillance following standard protocol including PSA, DRE and TRUS biopsies and intervention with multiparametric MRI + additional biopsies if suspicious lesions are found
Primary Outcome Measure Information:
Title
Changes in treatment from active surveillance (observation) to active treatment based on mp-MRI results.
Description
Patients enrolled in active surveillance will progress to active treatment if mp-MRI show previously undetected suspicious areas of significant disease. Significant cancer (measured by Gleason score and cancer core involvement on biopsies) will be confirmed by repeat biopsies of the suspicious areas. The decision to progress to active treatment is based on decision from the treating urologist.
Time Frame
12 months
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with low risk localized prostate cancer enrolled in active surveillance
Exclusion Criteria:
Metastatic prostate cancer
No mp-MRI data present
Prostate cancer treatment
Known allergic reaction to Gadolinium-based MRI contrast agent
Prostate biopsy during the last 21 days
Impaired renal function with GFR < 30 ml / min
pacemaker
Magnetic metal residues in the body
Claustrophobia
Psychiatric disorders
Age under 18 year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars Boesen, MD, PhD
Organizational Affiliation
Department of Urology, Herlev University Hospital Herleb, Herlev, Denmark, 2730
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Urology, Herlev University Hospital Herlev
City
Herlev
ZIP/Postal Code
2730
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Multiparametric MRI in Men With Prostate Cancer Enrolled in Active Surveillance
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