Multiparametric MRI in Men With Prostate Cancer Enrolled in Active Surveillance

Sponsor
Herlev Hospital (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT03648359
Collaborator
(none)
200
1
1
44
4.5

Study Details

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

Condition or Disease Intervention/Treatment Phase
  • Procedure: multiparametric MRI Diagnostics
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Multiparametric MRI in Men With Prostate Cancer Enrolled in Active Surveillance
Actual Study Start Date :
May 1, 2020
Anticipated Primary Completion Date :
Jan 1, 2024
Anticipated Study Completion Date :
Jan 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Enrolled AS patients

Patients with prostate cancer enrolled i active surveillance protocol using PSA, digital rectal examination and conventional TRUS-biopsies

Procedure: multiparametric MRI Diagnostics
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

Outcome Measures

Primary Outcome Measures

  1. Changes in treatment from active surveillance (observation) to active treatment based on mp-MRI results. [12 months]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Urology, Herlev University Hospital Herlev Herlev Denmark 2730

Sponsors and Collaborators

  • Herlev Hospital

Investigators

  • Principal Investigator: Lars Boesen, MD, PhD, Department of Urology, Herlev University Hospital Herleb, Herlev, Denmark, 2730

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lars Boesen, Primary investigator, MD, PhD, Herlev Hospital
ClinicalTrials.gov Identifier:
NCT03648359
Other Study ID Numbers:
  • AS
First Posted:
Aug 27, 2018
Last Update Posted:
Mar 28, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Lars Boesen, Primary investigator, MD, PhD, Herlev Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 28, 2022