The first and only test of its kind to identify patients who will NOT respond to AR-targeted therapies
Finding the most effective treatment for your patients with metastatic castration-resistant prostate cancer (mCRPC) can be a challenge. The Oncotype DX AR-V7 Nucleus Detect test helps you quickly and confidently determine the next step.
Accurately identify patients resistant to targeted therapies
Not all mCRPC patients respond to androgen receptor (AR)-targeted therapies, like abiraterone and enzalutamide.1 When AR-targeted therapy fails, acquired resistance could be the cause. The only predictive and prognostic test for men with mCRPC, the AR-V7 Nucleus Detect test:
- Accurately identifies patients who will not benefit from AR-targeted therapies.
- Is predictive of improved overall survival with taxanes versus AR-targeted therapies.
- Provides easy-to-interpret results (a positive or negative result).
The AR-V7 Nucleus Detect test provides unparalleled specificity by detecting AR-V7 proteins in the nucleus of circulating tumor cells (not cytoplasmic AR-V7 proteins). Find out more about nuclear detection.
Order the test each time the risk of resistance increases
Over time, tumors can adapt (and become resistant) to AR-targeted treatments. The percentage of patients who are nuclear AR-V7+ (an absolute indicator that a patient will not respond to AR-targeted therapies) increases with each exposure to AR-targeted therapies.2
- Roughly 1 in 5 patients (18%) are nuclear AR-V7+ after receiving abiraterone or enzalutamide.
- Roughly 1 in 3 patients (31%) are nuclear AR-V7+ after receiving two rounds of AR-targeted therapy.
The percentage of mCRPC patients with the AR splice variant (AR-V7+) increased with continued exposure to AR-targeted therapies2
Cross-sectional cohort study. Blood samples were collected from 161 patients with mCRPC and tested for the presence of AR-V7.
No intrusive procedures required
A liquid biopsy, the AR-V7 Nucleus Detect test analyzes circulating tumor cells in the patient’s blood. The sample is obtained through a simple blood draw and sent to our clinical laboratory. No intrusive or complicated procedures are required. The results are reported to the ordering physician confirming the patient as either AR-V7+ or AR-V7-. Learn how to order and use the AR-V7 Nucleus Detect test.