Transform the future of cancer screening with the Cancerguard™ test


~70% of annual cancer cases
and deaths have no
recommended screening3
With ~600,000 deaths in the
US every year, cancer is the
2nd deadliest disease4
Recommended screening only catches 1 in 7 cancers§,5
Only 4 types of cancer have recommended screening options3
The Cancerguard test dramatically expands your screening power
Helps find the deadliest cancers

Cancerguard screens for cancer types responsible for the majority of annual cancer diagnoses in the U.S. including the ones that are hardest to find.
With Cancerguard, you can expand your screening capabilities to enable more comprehensive proactive care.

Catching cancer earlier can change everything. The Cancerguard test found 1 in 3 early-stage cancers in a study.
You can help your patients move forward with confidence--and stay one step ahead of even the most aggressive cancers.

With high specificity, the Cancerguard test delivers actionable results.
Low false positive rates, which minimize unnecessary imaging and follow up, mean you can do more for your patients.
Multiple biomarker classes. Actionable results.
The only test of its kind to combine DNA methylation and protein biomarkers2
- Analyzing multiple biological signals casts a wider net for detecting cancer in its early stages.
- Our multi-biomarker class approach boosts detection of 6 of the deadliest cancer* organ types with the shortest 5-year survival rate.
- The Cancerguard test is designed to detect more than 50 cancer types and subtypes.
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Designed to minimize unnecessary follow-ups

Expert-designed imaging workflow
Less guesswork. Greater efficiency.
Showed a ~30% reduction in diagnostic burden
Trusted guidance to ease patient anxiety

Our Care Navigators can act as a patient’s personal guide after a positive test result and cover things like:
- Finding locations for follow-up imaging and testing
- Providing eligibility details for our Patient Imaging Reimbursement Program
- Help assess and reduce barriers to getting follow-up care

Coverage of follow-up imaging after a positive result varies based on insurance plans and a patient’s unique situation. If a patient has a positive test result, our imaging reimbursement program can help reduce the financial impact for eligible patients, so they can stay focused on their health. Patients must apply and eligibility depends on program qualifications and is not guaranteed.
The Imaging Reimbursement program will not reimburse any covered imaging costs, including copay, coinsurance and/or deductible amounts determined by insurance.
Results designed for clarity.
Negative Result
Positive Result
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Partnering with the brightest minds in cancer research
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Three ways to use DNA to gain insight

Multi-Cancer Early Detection (MCED) test

Hereditary Cancer Test
(HCT)

Molecular Residual Disease (MRD) test
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Footnotes and references
- pancreatic, esophageal, liver, lung, stomach, ovarian
- American Cancer Society. Cancer Facts & Figures 2025. Cancer.org. Published 2025.
- $689 amount reflects self-pay price. FSA/HSA/HRA programs may be a resource you could use to pay as well.
- Limitations: Based on modeling data derived from numerous sources including self-reported surveys. Includes assumptions on detectability of certain cancer types. Does not include all cancer types or screening methods.
- Data on file. Cancerguard Cancer Subtype Analysis. Exact Sciences, Madison, WI; September 2025
- Exact Sciences. Exact Sciences Specimen Collection Guide Preparation Collection and Processing. Published 2024, Accessed June 13, 2025
- Data on file. Cancerguard Test development study. 2025. Bioinformatics, Exact Sciences, Madison, WI
- Data on file. Calculated cancers without USPSTF recommended screening tests. 2025.
- Siegel RL, Kratzer TB, Giaquinto AN, Sung H, Jemal A. Cancer statistics, 2025. CA Cancer. J Clin. 2025;75(1):10‐45.
- NORC at the University of Chicago. Percent of Cancers Detected by Screening in the U.S. Published 2022. Accessed June 13, 2025
- Exact Sciences. Cancerguard™ Patient Support Guide. Published 2025 Accessed July 11, 2025.
- Exact Sciences. Patient Positive Result Supplement. Published 2025. Accessed July 11 2025
- Exact Sciences. Cancerguard™ Care Navigation Guide. Published 2025. Accessed July 23, 2025.
- Exact Sciences. Exact Sciences Company History. Published 2025. Accessed June 13, 2025
- Choudhry O, Kharge A, Rego S, et al. DETECT-A Participants with Pre-Malignant Conditions Diagnosed Consequent to an MCED Test.; 2024. Accessed June 13, 2025.
Important information about the Cancerguard test
Rx only. The Cancerguard™ test is indicated for use in adults ages 50-84 with no known cancer diagnosis in the last three years. It detects alterations in circulating tumor DNA and tumor-associated protein levels which are commonly associated with cancer. The test does not detect all cancers and is not a replacement for existing recommended cancer screening or diagnostic modalities for cancer. Current recommended screening for cancer should also be followed. The test is not indicated for screening of breast and prostate cancer and was not evaluated for the detection of pre-cancerous lesions. Due to the potential for follow-up imaging with IV contrast CT after a positive test result, careful consideration should be given before ordering the Cancerguard test for patients with a history of adverse reactions to iodine based IV contrast or for women who are, may be, or plan to become pregnant. Results should be interpreted in the context of a patient’s medical history, clinical signs, and symptoms. A negative result does not rule out the presence of cancer of any type. A positive Cancerguard™ test result means that the blood test identified a cancer signal that may indicate the presence of cancer. This result alone does not confirm the presence of cancer. Further clinical evaluation by a healthcare provider (which may include blood tests such as complete blood count and comprehensive metabolic panel) and follow-up imaging are needed to locate and confirm a diagnosis of cancer or determine that cancer is not present. While there are no established guidelines for imaging following a positive Cancerguard test result, there is a published follow-up workflow based on expert clinician opinion and results from an exploratory, prospective, interventional study [Kisiel et al Life (Basel) 2024 Jul 24; Lennon et al, Science, 2020]. The proposed workflow in the Kisiel et al publication includes an intravenous-contrast enhanced computed tomography (IV contrast CT of chest, abdomen/pelvis, and soft-tissue neck) and if necessary, positron emission tomography-computed tomography (18F FDG PET-CT) from the skull-base to mid-thigh. Alternative follow-up procedures (e.g. targeted imaging, endoscopic procedures, CT without IV- contrast) may be appropriate in the context of the patient’s medical history and clinical evaluation [Lennon et al, Science, 2020]. False positive and false negative test results can occur.
The Cancerguard test was developed, and the performance characteristics validated by Exact Sciences Laboratories following College of American Pathologists (CAP) and Clinical Laboratory Improvement Amendments (CLIA) regulations. This test has not been cleared or approved by the US Food and Drug Administration. The test is performed at Exact Sciences Laboratories. Exact Sciences Laboratories is accredited by CAP, certified under CLIA regulations, and qualified to perform high-complexity clinical laboratory testing.