A Registry for Hereditary Cancer Risk Assessment and Genetic Testing

Sponsor
Myriad Genetic Laboratories, Inc. (Industry)
Overall Status
Completed
CT.gov ID
NCT04015102
Collaborator
Carolina Urologic Research Center (Other)
255
10
19.8
25.5
1.3

Study Details

Study Description

Brief Summary

This prospective registry will evaluate the feasibility and impact of implementing standard cancer family history review and guideline-aligned genetic testing for men diagnosed with Prostate Cancer in community urology practices nationwide.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Genes linked to hereditary cancer syndromes have been associated with increased risk for prostate cancer (PrCa), earlier disease onset and increased disease aggressiveness.1,2 Ascertaining family cancer history and hereditary risk in men diagnosed with PrCa can help inform medical management decisions. Recently published National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology for Prostate Cancer (v3.2018)3 and Genetic/Familial High Risk Assessment: Breast and Ovarian (v2.2019)4 as well as the American Urological Association Guideline for Clinically Localized Prostate Cancer (2017)5 recommend appropriate counseling and genetic testing for men who are at increased hereditary cancer risk, based upon personal or family history. Genetic testing for patients with metastatic prostate cancer is now standard of care per NCCN Genetic/Familial High Risk Assessment: Breast and Ovarian (v2.2019) guidelines4. NCCN Prostate Cancer Guidelines (v3.2018)3 recommend obtaining a cancer-focused family history at diagnosis and consideration of germline genetic testing in multiple risk groups. Community urology practices can support guideline-aligned care by performing routine hereditary cancer risk assessment (HCRA), patient counseling and, when appropriate, genetic testing. This prospective registry will evaluate the feasibility and impact of implementing standard cancer family history review and guideline-aligned genetic testing for men diagnosed with PrCa in community urology practices nationwide.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    255 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    A Registry for Hereditary Cancer Risk Assessment and Genetic Testing Among Men With Prostate Cancer in the Community Urology Practice Setting
    Actual Study Start Date :
    Mar 6, 2019
    Actual Primary Completion Date :
    Oct 21, 2020
    Actual Study Completion Date :
    Oct 30, 2020

    Outcome Measures

    Primary Outcome Measures

    1. To see how practical it would be to integrate a standard hereditary cancer risk assessment, patient counseling and genetic testing process into the community urology practice setting. [18 weeks per site]

      To see how practical it would be to integrate a standard hereditary cancer risk assessment , patient counseling and genetic testing process into the community urology practice setting. Also to evaluate the impact of the integrated process on provider and patient satisfaction. This registry will gather information to evaluate the feasibility of HCRA and genetic testing process integration in the Urology community practice setting. Analysis of the registry will compare historical pre-process integration data with post-integration data from the same providers within participating community Urology practices.

    Secondary Outcome Measures

    1. To see what the proportion of community urology patients with PrCa is who complete each component of the HCRA, patient counseling and genetic testing process. [18 weeks]

      To see what the proportion of community urology patients with PrCa is who complete each component of the HCRA, patient counseling and genetic testing process. This registry will gather information to evaluate the feasibility of HCRA and genetic testing process integration in the Urology community practice setting. Analysis of the registry will compare historical pre-process integration data with post-integration data from the same providers within participating community Urology practices.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 18 Years of age or older at time of enrollment

    • Affected with Prostate Cancer (newly or previously diagnosed patients).

    • Presents for a medical care visit and meets eligibility criteria for hereditary cancer genetic testing, based on personal and family cancer history and NCCN Practice Guidelines in Oncology (Prostate Cancer)

    • Able to understand informed consent and agrees to participate in the registry.

    Exclusion Criteria:
    • Minors (younger than 18 years of age)

    • Have had previous genetic testing for Hereditary Breast and Ovarian Cancer or Lynch Syndrome, or have previously undergone hereditary multi-gene, pan-cancer, or panel testing.

    • Unable to provide routine clinical informed consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Arkansas Urology Little Rock Arkansas United States 72211
    2 Urology Associates of Central California Fresno California United States 93720
    3 Urologic Specialists of Northwest Indiana Merrillville Indiana United States 46410
    4 Comprehensive Urology Royal Oak Michigan United States 48073
    5 Comprehensive Urology Waterford Michigan United States 48328
    6 Associated Medical Professionals of New York Syracuse New York United States 13210
    7 Associated Urologists of North Carolina Raleigh North Carolina United States 27612
    8 Oregon Urology Institute Springfield Oregon United States 97477
    9 MidLantic Urology Bala-Cynwyd Pennsylvania United States 19004
    10 Carolina Urologic Research Center Myrtle Beach South Carolina United States 29572

    Sponsors and Collaborators

    • Myriad Genetic Laboratories, Inc.
    • Carolina Urologic Research Center

    Investigators

    • Principal Investigator: Neal Shore, MD, Carolina Urologic Research Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Myriad Genetic Laboratories, Inc.
    ClinicalTrials.gov Identifier:
    NCT04015102
    Other Study ID Numbers:
    • URO-012
    First Posted:
    Jul 10, 2019
    Last Update Posted:
    Nov 5, 2020
    Last Verified:
    Nov 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Myriad Genetic Laboratories, Inc.
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 5, 2020