Long-Term Prospective Registry in Prostate Cancer Patients From Diverse Urology Practice Settings Following Prolaris Testing

  • STATUS
    Recruiting
  • End date
    Nov 5, 2031
  • participants needed
    500
  • sponsor
    Myriad Genetic Laboratories, Inc.
Updated on 19 February 2024
adenocarcinoma
adenocarcinoma of prostate
prolaris testing

Summary

This registry will evaluate treatment selection for patients with newly diagnosed, localized prostate cancer following Prolaris testing. It will measure the proportion of men who initially select treatment with active surveillance, the time frame between active surveillance selection and any change in treatment, and clinical outcomes.

Description

To evaluate use of the Prolaris score in treatment management decisions in an ethnically and racially diverse population of men who have been newly diagnosed with prostate cancer and who are potential candidates for active surveillance. This registry will evaluate oncologic and co-morbidity outcomes in patients who receive Prolaris testing. Additionally, the registry will measure the prevalence and distribution of pathogenic mutations in hereditary cancer risk-associated genes among men with prostate cancer who meet National Cancer Center Network (NCCN) criteria for hereditary cancer genetic testing.

The primary objective of this registry is to evaluate initial selection of active surveillance (Active Surveillance selection) versus definitive therapy (DT) among men with newly diagnosed prostate cancer who make treatment decisions with Prolaris testing, and among patient subsets defined by race/ethnicity.

The secondary objectives of the registry are to evaluate progression of from Active Surveillance to definitive therapy over time and prostate cancer-associated morbidities that affect quality of life among men with newly diagnosed prostate cancer and who undergo Prolaris testing, and among patient subsets defined by racial/ethnic background and ancestry.

Details
Condition Malignant neoplasm of prostate, Prostatic disorder
Age 18-100 years
Clinical Study IdentifierNCT04404894
SponsorMyriad Genetic Laboratories, Inc.
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Age 18 years or older on date of enrollment
Diagnosed within the past six months with histologically proven, localized adenocarcinoma of prostate determined via transrectal ultrasonography and biopsy of at least 10 prostate sites
Received Prolaris testing and a resulting CCR score from the diagnostic biopsy sample as standard of care
Can be monitored for disease progression according to standard of care (e.g., current NCCN guidelines)

Exclusion Criteria

Estimated life expectancy < 10 years
Clinical evidence of metastasis or lymph node involvement
Received pelvic radiation prior to biopsy
Received androgen deprivation therapy (ADT) prior to biopsy; however, 5 alphareductase inhibitor (5-ARI) use is permitted
Plan to use PrCa-specific prognostic testing other than PSA for treatment decision making during Active Surveillance
Currently participating in an interventional clinical trial
Unable to provide routine clinical informed consent
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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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