Getting Started with the Empower Hereditary Cancer Test
Inherited mutations can significantly increase lifetime risk for developing cancer1
Learn More About Genetic Mutations & Hereditary Cancers
Hereditary Breast and Ovarian Cancer (HBOC) Syndrome
Up to 10% of all breast cancers can be attributed to hereditary causes, the most well known of which is a BRCA1 or 2 mutation. Inherited mutations can increase a woman’s risk for breast cancer to greater than 60%, yet up to 97% of women who carry that risk don’t know it. Patients who know their hereditary or familial cancer risk have better outcomes than those who don’t.1, 2
More Informed Treatment with Hereditary Cancer Testing
“Had I known that I carried the BRCA1 mutation when I was first diagnosed, I would have had the opportunity for different treatment options. It’s an important lesson for providers – talk about family cancer history.”
AMY V. – BRCA1 mutation carrier, breast cancer survivor
As many as 1 in 370 people are Lynch syndrome carriers, yet 95% of them do not know. Lynch syndrome is the most common inherited cause of colon cancer and endometrial cancer. In fact, gynecologic cancer is a hallmark of Lynch syndrome. Lynch syndrome can be identified early to manage cancer risk.3, 4, 5, 6, 7
How to identify and manage hereditary cancer risk
“I feel like the luckiest person in the world to have this information. I can be a previvor. I can take control of my health now and make sure that I don’t ever have to deal with uterine or colon cancer like every woman in my maternal line has so far.”
JENNIFER PLENT – Lynch syndrome mutation carrier, cancer previvor
How it works
Provider orders an Empower Hereditary Cancer Test.
Patient provides a blood or saliva sample.
Patients review results with their provider within 2 weeks.
Actionable reports guide next steps, including:
- Detect cancer at its earliest, most treatable stage
- Identify risk-reducing medications and surgeries
- Inform surgical and therapeutic decisions following a cancer diagnosis
- Notify family members to help them proactively manage hereditary cancer risk
Making the difference for families with hereditary cancer
“Our mom isn’t here to walk us through this journey.” Hannah and Katie made proactive health plans together after learning they carry a BRCA1 mutation.
Streamlined family cancer history intake with NEVA
- Streamlined family cancer history intake with NEVA
- Providers have a single view of patient risk assessment details and all Natera test orders