Open Registry Measuring Impact of Genomic Testing on Treatment Decision After Biopsy in Newly Diagnosed Prostate Cancer Patients



Status:Recruiting
Conditions:Prostate Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/13/2015
Start Date:May 2014
Contact:Kristen Rushton
Email:krushton@myriad.com

Use our guide to learn which trials are right for you!

An Open Registry to Measure the Impact of Adding Genomic Testing (Prolaris®) on the Treatment Decision Following Biopsy in Newly Diagnosed Prostate Cancer Patients by Specialists

This registry is intended to measure the impact of Prolaris® testing on therapeutic
decisions when added to standard clinical-pathological parameters in men with newly
diagnosed prostate cancer.


Inclusion Criteria:

- Newly diagnosed (≤6 months), untreated patients with histologically proven
adenocarcinoma of the prostate that have the following characteristics.

- Clinically localized (no evidence on clinical or imaging studies of advanced disease.

- No hormonal therapy including LHRH agonist or antagonist, anti-androgen, 5-alpha
reductase inhibitor, estrogens or exogenous androgens, when applicable.

- Sufficient amount of tissue remains from biopsy to perform genomic testing.

Exclusion Criteria:

- Patients with known history of hypogonadism will be excluded from the registry
We found this trial at
1
site
Seattle, Washington 98104
(206) 543-2100
Univ of Washington Founded in 1861 by a private gift of 10 acres in what...
?
mi
from
Seattle, WA
Click here to add this to my saved trials