Genomics in Michigan to AdJust Outcomes in Prostate canceR (G-MAJOR) for Men With Newly Diagnosed Favorable Risk Prostate Cancer
Primary Purpose
Prostate Cancer
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Decipher
Prolaris
Oncotype Dx Genomic Prostate Score (GPS)
Standard of care (askMUSIC score)
Sponsored by
About this trial
This is an interventional other trial for Prostate Cancer focused on measuring Biomarkers, Active surveillance, Gene Expression Classifier
Eligibility Criteria
Inclusion Criteria:
- Prostate cancer patients who have undergone diagnostic prostate biopsy in the past 9 months.
- Prostate biopsy tumor tissue (FFPR block) available for processing
- Age 18 years or older
- PSA <20 ng/ml
- Grade Group (GG) 1 cancer with > 2 biopsy cores involved with cancer OR GG2 cancer
- Ability to understand and the willingness to sign a written informed consent. A subject's legally acceptable representative may sign the consent form.
Exclusion Criteria:
- Clinical (on digital rectal exam) or radiographic evidence (if MRI performed) of T3 disease
- Nodal or metastatic prostate cancer (if staging imaging performed)
- Prior prostate cancer treatment, including prostatectomy, radiation therapy, or hormone therapy.
- Prior prostate gene expression classier testing
Sites / Locations
- University of Michigan Rogel Cancer CenterRecruiting
- Henry Ford Health SystemRecruiting
- Sherwood Medical CenterRecruiting
- Spectrum Health Medical GroupRecruiting
- Western Michigan Urological AssociatesRecruiting
- University of North CarolinaRecruiting
- University of Pennsylvania Perelman School of MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Standard of care (no pre-treatment genomics testing)
Standard of care + pre-treatment genomics testing
Arm Description
Provider will discuss askMUSIC results with patient prior to deciding on a management strategy (standard of care).
Provider will discuss askMUSIC and Gene Expression Classifier (GEC) results with patient prior to deciding on a cancer management strategy. Patients' biopsy tissue will be analyzed using one of the following GECs: Decipher, Prolaris or Oncotype Dx.
Outcomes
Primary Outcome Measures
Binomial proportion of men on active surveillance without treatment
Secondary Outcome Measures
Occurence of grade reclassification
Grade reclassification defined as an increase in grade group on surveillance biopsy (GG=1 to GG≥2 or GG=2 to GG≥3) for patients managed on active surveillance
Rate of indolent pathology
To determine the impact of GEC testing on the rate of potentially unnecessary surgery, as defined by indolent pathology at prostatectomy (GG1 and stage pT2).
Mean score per arm of patient reported urinary function questionnaire
Assessed by patient reported Expanded Prostate Cancer Index (EPIC) Urinary Incontinence Domain (UIN) questionnaire. Response options form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better quality of life (QOL).
Proportion of patients with changes from baseline in urinary function exceeding Minimal Important Differences (MID).
Assessed by patient reported EPIC UIN questionnaire. For this measure, MID = 9 points.
Mean score per arm of patient reported sexual function questionnaire
Assessed by patient reported Expanded Prostate Cancer Index (EPIC) sexual domain questionnaire. Response options form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better QOL.
Proportion of patients with changes from baseline in sexual function exceeding Minimal Important Differences (MID).
Assessed by patient reported EPIC sexual function questionnaire. For this measure, MID = 11 points.
Time to biochemical recurrence (BCR)
Time from treatment PSA >= 0.2 ng/mL for patients undergoing surgery (with PSA at least 5 weeks after surgery) and nadir plus 2.0 ng/mL for patients undergoing radiotherapy.
Time to distant metastases
Assessed by CT, MRI, bone scan, and/or PET scan
Mean score per arm of health-related quality of life (HRQOL)
Assessed by patient reported Expanded Prostate Cancer Index Composite short form (EPIC-26). EPIC-26 encompasses 5 domains (Urinary Incontinence, Urinary Irritative/Obstructive, Bowel, Sexual, and Hormonal). Response options for each of 26 items form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better HRQOL.
Rate of adverse pathology at prostatectomy
To determine the performance of GEC testing in predicting adverse pathology, defined as GG≥3 and/or ≥pT3 disease.
Rate of biochemical recurrence
To determine the performance of GEC testing in predicting biochemical recurrence, defined as PSA >= 0.2 ng/mL for patients undergoing surgery (with PSA at least 5 weeks after surgery) and nadir plus 2.0 ng/mL for patients undergoing radiotherapy.
Full Information
NCT ID
NCT04396808
First Posted
May 15, 2020
Last Updated
September 25, 2023
Sponsor
University of Michigan Rogel Cancer Center
Collaborators
National Institutes of Health (NIH), Myrexis Inc., Veracyte, Inc., MDx Health
1. Study Identification
Unique Protocol Identification Number
NCT04396808
Brief Title
Genomics in Michigan to AdJust Outcomes in Prostate canceR (G-MAJOR) for Men With Newly Diagnosed Favorable Risk Prostate Cancer
Official Title
Genomics in Michigan to AdJust Outcomes in Prostate canceR (G-MAJOR): A Randomized Multi-center Study for Men With Newly Diagnosed Favorable Risk Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 5, 2020 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
November 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Michigan Rogel Cancer Center
Collaborators
National Institutes of Health (NIH), Myrexis Inc., Veracyte, Inc., MDx Health
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.
Yes
5. Study Description
Brief Summary
This study seeks to determine the clinical impact of Gene Expression Classifier (GEC) testing in prostate cancer care while also developing a pragmatic approach for improved GEC clinical use and future study.
Detailed Description
All patients in this study have received or will receive a score from the Michigan Urological Surgery Improvement Collaborative's Cancer of the Prostate Risk Assessment (askMUSIC) scoring system, at the time of enrollment. AskMUSIC is a risk calculator based on standard clinical and pathologic variables and is generally included as part of routine clinical care. The variables used in the risk calculator are prostate-specific antigen (PSA), Gleason score, number of positive core biopsies, number of negative core biopsies, and clinical stage.
Patients will be randomized to either an intervention arm or a control arm. In the control arm, the treating provider will review the askMUSIC score with the patient. In the intervention arm, the treating provider will review the askMUSIC and the GEC score with the patient. Biopsies obtained during the course of standard clinical care will be analyzed using one of the following GECs: Decipher, Prolaris or Oncotype Dx Genomic Prostate Score. No additional biopsies will be obtained as part of this study.
After reviewing the results, patients and their treating physicians will decide on a management strategy.
Long-term follow-up will be tracked through the Michigan Urological Surgery Improvement Collaborative (MUSIC) registry.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Biomarkers, Active surveillance, Gene Expression Classifier
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
1:1 cluster-crossover in 3 month blocks
Masking
None (Open Label)
Allocation
Randomized
Enrollment
900 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard of care (no pre-treatment genomics testing)
Arm Type
Active Comparator
Arm Description
Provider will discuss askMUSIC results with patient prior to deciding on a management strategy (standard of care).
Arm Title
Standard of care + pre-treatment genomics testing
Arm Type
Active Comparator
Arm Description
Provider will discuss askMUSIC and Gene Expression Classifier (GEC) results with patient prior to deciding on a cancer management strategy. Patients' biopsy tissue will be analyzed using one of the following GECs: Decipher, Prolaris or Oncotype Dx.
Intervention Type
Device
Intervention Name(s)
Decipher
Other Intervention Name(s)
Decipher Prostate Cancer Classifier
Intervention Description
The Decipher test (GenomeDx Biosciences) is a genomic test that will be performed on prostate biopsy tissue. Results will be provided to the patient and physician prior to making a treatment decision.
Intervention Type
Device
Intervention Name(s)
Prolaris
Other Intervention Name(s)
Prolaris Prostate Cancer Test
Intervention Description
The Prolaris test (Myriad Genetics, Inc.) is a genomic test that will be performed on prostate biopsy tissue. Results will be provided to the patient and physician prior to making a treatment decision.
Intervention Type
Device
Intervention Name(s)
Oncotype Dx Genomic Prostate Score (GPS)
Intervention Description
The Oncotype Dx GPS test (Exact Sciences corp.) is a genomic test that will be performed on prostate biopsy tissue. Results will be provided to the patient and physician prior to making a treatment decision.
Intervention Type
Other
Intervention Name(s)
Standard of care (askMUSIC score)
Other Intervention Name(s)
askMUSIC score
Intervention Description
AskMUSIC is a risk calculator based on standard clinical and pathologic variables (https://ask.musicurology.com/) and is generally included as part of routine clinical care.
Primary Outcome Measure Information:
Title
Binomial proportion of men on active surveillance without treatment
Time Frame
At 2 years
Secondary Outcome Measure Information:
Title
Occurence of grade reclassification
Description
Grade reclassification defined as an increase in grade group on surveillance biopsy (GG=1 to GG≥2 or GG=2 to GG≥3) for patients managed on active surveillance
Time Frame
At 2 years
Title
Rate of indolent pathology
Description
To determine the impact of GEC testing on the rate of potentially unnecessary surgery, as defined by indolent pathology at prostatectomy (GG1 and stage pT2).
Time Frame
At time of prostatectomy (for patients who undergo procedure), up to 2 years
Title
Mean score per arm of patient reported urinary function questionnaire
Description
Assessed by patient reported Expanded Prostate Cancer Index (EPIC) Urinary Incontinence Domain (UIN) questionnaire. Response options form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better quality of life (QOL).
Time Frame
At 2 years
Title
Proportion of patients with changes from baseline in urinary function exceeding Minimal Important Differences (MID).
Description
Assessed by patient reported EPIC UIN questionnaire. For this measure, MID = 9 points.
Time Frame
Baseline to 12 months and 2 years
Title
Mean score per arm of patient reported sexual function questionnaire
Description
Assessed by patient reported Expanded Prostate Cancer Index (EPIC) sexual domain questionnaire. Response options form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better QOL.
Time Frame
At 2 years
Title
Proportion of patients with changes from baseline in sexual function exceeding Minimal Important Differences (MID).
Description
Assessed by patient reported EPIC sexual function questionnaire. For this measure, MID = 11 points.
Time Frame
Baseline to 12 months and 2 years
Title
Time to biochemical recurrence (BCR)
Description
Time from treatment PSA >= 0.2 ng/mL for patients undergoing surgery (with PSA at least 5 weeks after surgery) and nadir plus 2.0 ng/mL for patients undergoing radiotherapy.
Time Frame
From time of radical therapy until the event or the last measured follow-up, up to 2 years
Title
Time to distant metastases
Description
Assessed by CT, MRI, bone scan, and/or PET scan
Time Frame
From time of radical therapy until the event or the last measured follow-up, up to 2 years
Title
Mean score per arm of health-related quality of life (HRQOL)
Description
Assessed by patient reported Expanded Prostate Cancer Index Composite short form (EPIC-26). EPIC-26 encompasses 5 domains (Urinary Incontinence, Urinary Irritative/Obstructive, Bowel, Sexual, and Hormonal). Response options for each of 26 items form a Likert scale, and multi-item scale scores are transformed linearly to a 0-100 scale, with higher scores representing better HRQOL.
Time Frame
At 2 years
Title
Rate of adverse pathology at prostatectomy
Description
To determine the performance of GEC testing in predicting adverse pathology, defined as GG≥3 and/or ≥pT3 disease.
Time Frame
At time of prostatectomy, up to 5 years from enrollment
Title
Rate of biochemical recurrence
Description
To determine the performance of GEC testing in predicting biochemical recurrence, defined as PSA >= 0.2 ng/mL for patients undergoing surgery (with PSA at least 5 weeks after surgery) and nadir plus 2.0 ng/mL for patients undergoing radiotherapy.
Time Frame
Up to 5 years following treatment
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Prostate cancer patients who have undergone diagnostic prostate biopsy in the past 9 months.
Prostate biopsy tumor tissue (FFPR block) available for processing
Age 18 years or older
PSA <20 ng/ml
Grade Group (GG) 1 cancer with > 2 biopsy cores involved with cancer OR GG2 cancer
Ability to understand and the willingness to sign a written informed consent. A subject's legally acceptable representative may sign the consent form.
Exclusion Criteria:
Clinical (on digital rectal exam) or radiographic evidence (if MRI performed) of T3 disease
Nodal or metastatic prostate cancer (if staging imaging performed)
Prior prostate cancer treatment, including prostatectomy, radiation therapy, or hormone therapy.
Prior prostate gene expression classier testing
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
G-Major Study
Phone
734-764-4060
Email
gmajorstudy@med.umich.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Todd Morgan, M.D.
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Daniel Spratt, M.D.
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan Rogel Cancer Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
G-Major Study
Phone
734-764-4060
Email
gmajorstudy@med.umich.edu
First Name & Middle Initial & Last Name & Degree
Todd Morgan, M.D.
First Name & Middle Initial & Last Name & Degree
Daniel Spratt, M.D.
Facility Name
Henry Ford Health System
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Craig Rogers, MD
Facility Name
Sherwood Medical Center
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48221
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Conrad Maitland, MD
Facility Name
Spectrum Health Medical Group
City
Grand Rapids
State/Province
Michigan
ZIP/Postal Code
49503
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Conrad Tobert
First Name & Middle Initial & Last Name & Degree
Conrad Tobert
Facility Name
Western Michigan Urological Associates
City
Holland
State/Province
Michigan
ZIP/Postal Code
49423
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Ludlow, MD
Facility Name
University of North Carolina
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ray Tan
First Name & Middle Initial & Last Name & Degree
Ray Tan
Facility Name
University of Pennsylvania Perelman School of Medicine
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hanna Stambakio
Phone
215-614-5039
Email
Hanna.Stambakio@pennmedicine.upenn.edu
First Name & Middle Initial & Last Name & Degree
Daniel Lee, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Genomics in Michigan to AdJust Outcomes in Prostate canceR (G-MAJOR) for Men With Newly Diagnosed Favorable Risk Prostate Cancer
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