Benefits of the Riskguard test

Being proactive now can make a difference for the future

A health care provider with stethoscope looking at a tablet device with a patient.
Powerful information about hereditary cancer risk
While many people have a history of cancer in their families, only 10-15% of cancers are hereditary.1 By testing for hereditary cancer conditions, patients and healthcare providers can better determine the optimal monitoring or treatment plan. 

The Riskguard test can offer powerful insights for patients who have a family history of cancer, patients who have been newly diagnosed with cancer, and even patients who have already undergone cancer treatment.

A man sitting in a chair receiving chemotherapy, gazing off to the right with a mobile device in his hand.
Tools for personalized treatment and risk-management
The Riskguard test can help patients and providers tailor individualized treatment and risk-management journeys, guided by genetics.2-7
An older man and woman with a younger woman, all smiling at the camera.
Results that empower you and your family members
Receive easy-to-understand results with potential next steps that providers and patients can use for personalized care planning.

The Riskguard test can also identify family members at risk and help them make more informed decisions about strategies to reduce their cancer risk. 

The Riskguard test checks 59 genes across 11 common cancer types
Approximately 1 in 8 cancers are due to a hereditary syndrome.1 The Riskguard test helps patients learn more about their genetic risk for some of the most common and aggressive cancer types.

Colorectal     Breast     Prostate     Pancreatic     Ovarian     Endometrial     Skin     Gastric     Kidney     Endocrine     Lung

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The Riskguard test process

Determine whether the Riskguard test is a good fit

Take the test — both in-office and at-home tests are available

Access the results online and discuss next steps

You have coverage options

We understand navigating coverage can be overwhelming. Exact Sciences* is an in-network provider with many health plans. We offer insurance billing and flexible payment options.

  • Coverage for eligible patients including Medicare and commercial insurance
  • Specialized support for billing insurance and prior authorization
  • Flexible payment options for patients
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We're here for you

With questions about ordering the Riskguard test, insurance billing and payment options, checking results, or getting connected with a genetic counselor, call us at +1 866-662-6897 or email us at riskguard@exactsciences.com.

References

  1. Genomic Health, Inc., an Exact Sciences company, is the billing entity for Riskguard.
  2. Medicare and commercial insurance plans have specific inclusion criteria based on personal and family history of cancer.

  1. DeBortoli E, McGahan E, Yanes T, et al., “ Utility of Germline, Somatic and ctDNA Testing in Adults With Cancer,” Cancer Medicine 14, no. 15 (2025): e71080, https://doi.org/10.1002/cam4.71080.
  2. Geyer CE Jr, Garber JE, Gelber RD, et al. OlympiA Clinical Trial Steering Committee and Investigators. Overall survival in the OlympiA phase III trial of adjuvant olaparib in patients with germline pathogenic variants in BRCA1/2 and high-risk, early breast cancer. Ann Oncol. 2022;33(12):1250-1268.
  3. Hussain M, Mateo J, Fizazi K, et al. PROfound Trial Investigators. Survival with olaparib in metastatic castration-resistant prostate cancer. N Engl J Med. 2020;383(24):2345-2357.
  4. Golan T, Hammel P, Reni M, et al. Maintenance olaparib for germline BRCA-mutated metastatic pancreatic cancer. N Engl J Med. 2019;381:317-327.
  5. Ledermann J, Harter P, Gourley C, et al. Olaparib maintenance therapy in patients with platinum-sensitive relapsed serous ovarian cancer: A preplanned retrospective analysis of outcomes by BRCA status in a randomised phase 2 trial. Lancet Oncol. 2014;15:852-861.
  6. Domchek SM, Friebel TM, Singer CF, et al. Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality. JAMA. 2010;304(9):967-975.
  7. Ladabaum U, Wang G, Terdiman J, et al. Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis. Ann Intern Med. 2011;155(2):69-79.