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Prostate Cancer Screening With Abbreviated MRI Protocol (ProstaPilot)

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Czechia
Study Type
Interventional
Intervention
magnetic resonance
serum PSA examination
Biopsy
Sponsored by
Masaryk Memorial Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prostate Cancer focused on measuring magnetic resonance imaging, biparametric MRI, prostate cancer, PI-RADS, PSA, preventive medicine

Eligibility Criteria

50 Years - 69 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria: Age 50-69 years Life expectancy over 10 years Ability to undergo all planned procedures (without contraindications to MRI or biopsy) No known prostate cancer or prostate biopsy in the past (interventions for BPH are not a restriction) No PSA test or prostate MRI in the past 2 years. No signs of prostatitis or urinary tract infection in the past 6 months. Signed informed consent. Exclusion Criteria: Contraindications to MRI Hip replacement Known BRCA1/BRCA2 mutation

Sites / Locations

  • Masaryk Memorial Cancer InstituteRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Preventive prostate examination by bpMRI

Arm Description

The cohort consists of patients: with age 50-69 years without any contraindications to MRI or biopsy without known status of prostate cancer or prostate biopsy in the past (interventions for BPH are not a restriction) without known BRCA mutation without PSA test or prostate MRI in the past 2 years without any signs of prostatitis or urinary tract infection in the past 6 months.

Outcomes

Primary Outcome Measures

Assessment of the importance of the imaging test in the screening of significant prostate cancer in asymptomatic men, compared with PSA screening: Proportion of positive MRI findings
Proportion of positive MRI findings (PI-RADS 4+) in the general population of men aged 50-69 years.
Distribution of PI-RADS scores in the observed cohort.
Distribution of PI-RADS scores (proportion of individual scores 1-5) in the screened population.
Proportion of positive PI-RADS detections in the cohort of patients indicated for biopsy.
Ratio of significant and non-significant cancers in individual categories of PI-RADS scores in patients indicated for biopsy.

Secondary Outcome Measures

Feasibility evaluation of a larger-scale study of screening for significant prostate cancer using an imaging modality:
Concordance rate (%) between radiologists performing MRI scoring.
Evaluation of complications after an interventional procedure (biopsy).
Number of complications after biopsy.
Evaluation of patient adherence to preventive examination - active recruitment.
Number of participants who agreed to be included in the study through used recruitment strategies.
Patient adherence to preventive examination - self-recruitment.
Number of participants who contacted the team themselves with a request for testing.
Patient adherence to preventive examination.
Number of participants who signed the informed consent and were enrolled in the study.
Evaluation of patient adherence to preventive examination.
Number of participants who visited a screening facility.
Evaluation of patient adherence to preventive examination - completation of planned exams.
Number of participants who completed the designated examination.
Evaluation of the financial burden of the study for the future preventive program of prostate cancer screening.
Costs of individual inclusion and screening tests.
Detection and assessment of potential barriers to patient participation in the study. Assessment of patient adherence to remain in the study throughout the study period.
Numbers and reasons of participants who did not complete scheduled tests, follow-up examinations, or withdrew informed consent.

Full Information

First Posted
September 2, 2022
Last Updated
October 30, 2022
Sponsor
Masaryk Memorial Cancer Institute
Collaborators
Masaryk University
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1. Study Identification

Unique Protocol Identification Number
NCT05603351
Brief Title
Prostate Cancer Screening With Abbreviated MRI Protocol
Acronym
ProstaPilot
Official Title
ProstaPilot: Prostate Cancer Screening Using MRI With an Abbreviated Protocol
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2022 (Actual)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Masaryk Memorial Cancer Institute
Collaborators
Masaryk University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Prostate cancer is one of the most common malignancies in the male population with incidence and mortality rates comparable to breast cancer in women, but in contrast, a population screening program that would fulfill all the recommended criteria is not yet available. According to international recommendations, the preventive PSA sampling used in clinical practice is not suitable because of the concurrent detection of clinically insignificant carcinomas in a major proportion of tests. These clinically non-significant cancers make up a significant and increasing proportion with age. Detection of non-significant cancers burdens the health care system and patients with the care that has no positive impact on their health. Current preventive serum prostate-specific antigen (PSA) testing does not distinguish benign hyperplasia and nonsignificant carcinoma from clinically significant cancer. It is therefore not suitable for full-scale screening. According to current guidelines, magnetic resonance imaging (MRI) is indicated only in patients with an increased risk of cancer for detection or staging after biopsy and is not used for screening. According to recent studies, MRI has detected an increased proportion of significant cancers in the general population compared to screening based on PSA, while fewer clinically insignificant cancers have been detected. In screening, a shorter examination protocol without contrast medium (biparametric MRI) is used with a lower cost per examination, allowing to increase both the number of patients examined and patient comfort. The main objective of the project is to assess the contribution of imaging in the screening of clinically significant prostate cancer and to validate the published results in the Czech population, and extend the screening model by the second round of examinations and additional laboratory markers. The secondary aim is to design a subsequent study with a larger number of participants allowing statistical evaluation, similar to the successful breast cancer screening.
Detailed Description
A prospective cross-sectional (with a longitudinal component, 2nd screening round) study evaluating the possibility of using the biparametric MRI protocol technique for screening clinically significant prostate cancer in men from the general population. Tests performed: Serum PSA PHI calculation (Prostate Health Index) to be performed only if the PSA values are in the range of 2-10 ng/l MRI of the prostate (abbreviated biparametric protocol) Digital rectal examination (DRE) as part of a clinical visit at a urologist in patients with a positive PSA test Biopsy - if indicated MRI specifications: Protocol with anatomical T2 sequence and diffusion-weighted images (DWI), according to the standards Typical complete examination time does not exceed 20 minutes, planned acquisition time less than 15 minutes. No contrast agent or spasmolytics is injected. Blinding: Every test evaluator (radiologist/urologist) does not know the results of other tests. · MRI reports entered in the registry obligatorily before the biopsy. The patient is not informed which test was positive and resulted in an indication for biopsy. The pathologist does not know the results of MRI or laboratory tests. The sequence of tests: The MRI is assessed with the PI-RADS 2.1 system, each finding is reported on a scale of 1-5. To minimize the detection of non-significant cancers and to reduce the number of biopsies according to the results of the IP1-Prostagram study, a PI-RADS value of 4-5 was chosen as a positive test representation. Consensual double reading by 2 experienced uroradiologists (at least 400 MRI of the prostate read by the beginning of the study). Men with a positive MRI test are planned for a targeted MRI/US fusion and systematic prostate biopsy. Men with a positive blood marker (either PSA, PSAD, or PHI) are planned for a systematic 12 core biopsy. Positive test results are PSA ≥ 3, integrated marker PSAD ≥ 0.15, and PHI ≥ 35. Study participants are invited to repeat the screening tests after 2 years by letter. If they do not respond to a written offer, also by e-mail and SMS. Definition of clinically significant cancer: • ISUP Grade Group ≥ 2.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
magnetic resonance imaging, biparametric MRI, prostate cancer, PI-RADS, PSA, preventive medicine

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A prospective cross-sectional (with a longitudinal component, 2nd screening round) study evaluating the possibility of using the abbreviated bpMRI protocol technique for screening clinically significant prostate cancer in men from the general population.
Masking
None (Open Label)
Allocation
N/A
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Preventive prostate examination by bpMRI
Arm Type
Experimental
Arm Description
The cohort consists of patients: with age 50-69 years without any contraindications to MRI or biopsy without known status of prostate cancer or prostate biopsy in the past (interventions for BPH are not a restriction) without known BRCA mutation without PSA test or prostate MRI in the past 2 years without any signs of prostatitis or urinary tract infection in the past 6 months.
Intervention Type
Diagnostic Test
Intervention Name(s)
magnetic resonance
Other Intervention Name(s)
MRI
Intervention Description
biparametric MRI with protocol including anatomical T2 sequence and diffusion-weighted images (DWI), according to the standards
Intervention Type
Diagnostic Test
Intervention Name(s)
serum PSA examination
Intervention Description
testing of prostate-specific antigen (PSA) in serum
Intervention Type
Procedure
Intervention Name(s)
Biopsy
Intervention Description
Men with a positive MR test are planned for a targeted MRI/US fusion and systematic prostate biopsy. Men with a positive blood marker (either PSA, PSAD, or PHI) are planned for a systematic 12 core biopsy. Positive test results are PSA ≥ 3, integrated marker PSAD ≥ 0.15, and PHI ≥ 35.
Primary Outcome Measure Information:
Title
Assessment of the importance of the imaging test in the screening of significant prostate cancer in asymptomatic men, compared with PSA screening: Proportion of positive MRI findings
Description
Proportion of positive MRI findings (PI-RADS 4+) in the general population of men aged 50-69 years.
Time Frame
2 years
Title
Distribution of PI-RADS scores in the observed cohort.
Description
Distribution of PI-RADS scores (proportion of individual scores 1-5) in the screened population.
Time Frame
2 years
Title
Proportion of positive PI-RADS detections in the cohort of patients indicated for biopsy.
Description
Ratio of significant and non-significant cancers in individual categories of PI-RADS scores in patients indicated for biopsy.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Feasibility evaluation of a larger-scale study of screening for significant prostate cancer using an imaging modality:
Description
Concordance rate (%) between radiologists performing MRI scoring.
Time Frame
2 years
Title
Evaluation of complications after an interventional procedure (biopsy).
Description
Number of complications after biopsy.
Time Frame
2 years
Title
Evaluation of patient adherence to preventive examination - active recruitment.
Description
Number of participants who agreed to be included in the study through used recruitment strategies.
Time Frame
2 years
Title
Patient adherence to preventive examination - self-recruitment.
Description
Number of participants who contacted the team themselves with a request for testing.
Time Frame
2 years
Title
Patient adherence to preventive examination.
Description
Number of participants who signed the informed consent and were enrolled in the study.
Time Frame
2 years
Title
Evaluation of patient adherence to preventive examination.
Description
Number of participants who visited a screening facility.
Time Frame
2 years
Title
Evaluation of patient adherence to preventive examination - completation of planned exams.
Description
Number of participants who completed the designated examination.
Time Frame
2 years
Title
Evaluation of the financial burden of the study for the future preventive program of prostate cancer screening.
Description
Costs of individual inclusion and screening tests.
Time Frame
2 years
Title
Detection and assessment of potential barriers to patient participation in the study. Assessment of patient adherence to remain in the study throughout the study period.
Description
Numbers and reasons of participants who did not complete scheduled tests, follow-up examinations, or withdrew informed consent.
Time Frame
2 years

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Due to the nature of examined organ (prostate), this study is focused exclusively on men.
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 50-69 years Life expectancy over 10 years Ability to undergo all planned procedures (without contraindications to MRI or biopsy) No known prostate cancer or prostate biopsy in the past (interventions for BPH are not a restriction) No PSA test or prostate MRI in the past 2 years. No signs of prostatitis or urinary tract infection in the past 6 months. Signed informed consent. Exclusion Criteria: Contraindications to MRI Hip replacement Known BRCA1/BRCA2 mutation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michal Standara, MD
Phone
00420 543 136 008
Email
standara@mou.cz
First Name & Middle Initial & Last Name or Official Title & Degree
Jan Křístek, MD, PhD
Phone
00420 605 444 732
Email
jan.kristek@mou.cz
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michal Staník, MD,PhD.
Organizational Affiliation
Masaryk Memorial Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Masaryk Memorial Cancer Institute
City
Brno
State/Province
Czech Republic
ZIP/Postal Code
65653
Country
Czechia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michal Standara, MD
Phone
+420543136008
Email
standara@mou.cz
First Name & Middle Initial & Last Name & Degree
Jan Kristek, Ph.D., MD
Phone
+420605444732
Email
jan.kristek@mou.cz
First Name & Middle Initial & Last Name & Degree
Michal Stanik, Ass.Prof.
First Name & Middle Initial & Last Name & Degree
Michal Standara, MD
First Name & Middle Initial & Last Name & Degree
Jan Kristek, PhD
First Name & Middle Initial & Last Name & Degree
Alexandr Poprach, Ass.Prof.
First Name & Middle Initial & Last Name & Degree
Milos Pacal, MD
First Name & Middle Initial & Last Name & Degree
Iva Babankova, MD
First Name & Middle Initial & Last Name & Degree
David Miklanek, MD

12. IPD Sharing Statement

Plan to Share IPD
No
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Links:
URL
https://www.uroweb.cz/index.php?pg=odborne-analyzy-a-publikace--epidemiologie-nadoru-urogenitalniho-systemu-v-ceske-republice
Description
Prostate cancer epidemiology in the Czech republic.
URL
https://www.svod.cz
Description
Epidemiology of malignant tumors in the Czech republic

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Prostate Cancer Screening With Abbreviated MRI Protocol

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