Long-term Study to Evaluate and Clinical Outcomes in Patients With Favorable Intermediate Risk Localized Prostate Cancer
a study on Prostate Cancer
This is a long-term prospective registry study to determine whether Prolaris testing in patients with favorable intermediate risk prostate cancer influences physician management decisions toward conservative treatment in patients with Prolaris low-risk scores without negatively impacting patient oncologic outcomes, thereby sparing low-risk patients from unnecessary treatments and associated side-effects.
Long-Term Prospective Registry to Evaluate Treatment Decisions and Clinical Outcomes in Patients With Favorable Intermediate-Risk Localized Prostate Cancer Following Cell Cycle Progression (CCP) Testing (Prolaris® Test)
This is a long-term prospective registry to evaluate the impact of Prolaris testing on therapeutic decisions in patients with newly diagnosed favorable intermediate-risk localized prostate cancer and to summarize clinical oncologic outcomes. The design of the study is non-interventional, and therefore the protocol will not require a specific treatment plan for study participants. However, in the absence of a universally accepted timeframe for repeat biopsies within existing active surveillance recommendations, study sites will be encouraged to monitor patients for disease progression as per the standard of care (e.g., current National Comprehensive Cancer Network [NCCN] guidelines) with the expectation of a repeat biopsy within 18 months of the initial biopsy. Patients who undergo Prolaris testing will be included in the registry as well as patients who do not undergo Prolaris testing. Data collection for the first primary objective extends over a 3-year period. During this time, data is collected on the treatment initiated, any follow-up prostate biopsy performed in patients initially treated with active surveillance, definitive treatments performed (with pathology data if surgical therapy is performed), and the reasons definitive treatment was pursued, as well as data related to disease progression such as biochemical recurrence, development of prostate cancer metastases, or disease specific death. Data collection for the second primary objective extends out to 8 years. During this time data is collected on any follow-up prostate biopsy in patients still treated with active surveillance, definitive treatments performed (with pathology data if surgical therapy is performed), and the reasons definitive treatment was pursued, as well as data related to disease progression such as biochemical recurrence, development of prostate cancer metastases, or disease specific death.
Prostate Cancer Prolaris Cell Cycle Progression Test Prostatic Neoplasms Prolaris Testing
You can join if…
Open to males ages 65 years and up
- Patients who have undergone CCP testing and patients who have not undergone CCP testing will be considered for enrollment in the study.
- Willing to provide written informed consent.
- Males ≥65 years old.
- Newly diagnosed (≤6 months), treatment-naïve patient with histologically proven localized adenocarcinoma of prostate whose initial treatment has not been decided.
- Candidate for and considering AS and yet would be eligible for definitive therapy.
- Favorable intermediate-risk disease, defined by the NCCN as follows:
- predominant Gleason grade 3; AND
- percentage of positive cores <50%; AND
- no more than 1 of the following NCCN intermediate-risk factors:
- Gleason grade 7
- PSA 10-20 ng/mL
- Estimated life expectancy ≥10 years.
- Can be monitored for disease progression according to standard of care (e.g., current NCCN guidelines).
You CAN'T join if...
- Clinical evidence of metastasis or lymph node involvement.
- Received pelvic radiation prior to biopsy.
- Received androgen deprivation therapy (ADT) prior to biopsy; however, 5 alpha-reductase inhibitors (5-ARIs) are permitted.
- Participation in interventional clinical trials.
- Patient is considering watchful waiting.
- Has a known history of hypogonadism.
- UCI Medical Center
accepting new patients
Orange California 92866 United States
- VA Long Beach Healthcare
accepting new patients
Long Beach California 90822 United States
- accepting new patients
- Start Date
- Completion Date
- Myriad Genetic Laboratories, Inc.
- Study Type
- Observational [Patient Registry]
- Last Updated
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study. Submitting your contact information does not obligate you to participate in research.
The study team should get back to you in a few business days.