Empowered Myriad Oncology patient

Each step. Every patient. Myriad Oncology.

Delivering comprehensive care at every step of the patient journey with germline and tumor genomic insights to assess hereditary cancer risk, guide treatment selection, and evaluate recurrence risk—all in one streamlined solution.

Empowering confident cancer care at every step

Myriad Oncology offers comprehensive germline and tumor genomic tests that provide clinically actionable insights, helping to tailor treatments for each patient’s unique cancer journey—maximizing their chance for a healthier future.

I’m a provider

I’m a patient

Improving patients outcomes throughout their journey

From risk assessment to therapy selection, Myriad Oncology offers integrated germline and tumor genomic tests that enable a truly personalized approach to cancer prevention and treatment.

Infographic of the simplified approach to Myriad Oncology’s patient pathway showing the different Myriad Oncology tests available for high-risk unaffected, diagnosed, progression, and survivorship patient types.Infographic of the simplified approach to Myriad Oncology’s patient pathway showing the different Myriad Oncology tests available for high-risk unaffected, diagnosed, progression, and survivorship patient types.

Comprehensive support services for providers and patients

Myriad Oncology provides a comprehensive suite of services and workflow solutions that simplify germline and tumor genomic testing, all at no additional cost to the clinic or patient.

Patient education

Pre- and post-test education as live, point-of-care sessions with a board-certified Genetic Counselor

Affordability

Transparent pricing with personalized cost estimates, financial assistance, and other affordability options, including direct pay

Fast results

Consolidated germline and tumor genomic results are available on average of 14 days after lab receives the sample

Easy reporting

The Myriad Management Tool streamlines germline and tumor genomic results into an easy-to-follow report

Provider support

Medical Science Liaison’s support providers and their teams in answering clinical, testing, and results-related questions

Lifetime commitment

Myriad’s Variant Classification Program includes a Lifetime Reclassification Commitment to send amended reports if a variant of uncertain significance (VUS) is reclassified and is clinically actionable

Comprehensive support services for providers and patients

Myriad Oncology provides a comprehensive suite of services and workflow solutions that simplify germline and tumor genomic testing, all at no additional cost to the clinic or patient.

Patient education

Pre- and post-test education as live, point-of-care sessions with a board-certified Genetic Counselor

Affordability

Transparent pricing with personalized cost estimates, financial assistance, and other affordability options, including direct pay

Fast results

Consolidated germline and tumor genomic results are available on average of 14 days after lab receives the sample

Easy reporting

The Myriad Management Tool streamlines germline and tumor genomic results into an easy-to-follow report

Provider support

Medical Science Liaison’s support providers and their teams in answering clinical, testing, and results-related questions

Lifetime commitment

Myriad’s Variant Classification Program includes a Lifetime Reclassification Commitment to send amended reports if a variant of uncertain significance (VUS) is reclassified and is clinically actionable

Myriad Oncology empowers providers and patients with fast, comprehensive answers to guide management decisions and targeted therapy choices

Comprehensive germline and tumor genomic biomarker testing from a single, trusted source

  • Germline Tests

    Germline hereditary cancer test that evaluates 48 clinically actionable genes to provide a comprehensive, guideline-driven assessment across 11 common cancer sites.

  • Tumor Profiling

    Precise Tumor® is a pan-cancer, comprehensive laboratory test that uses state-of-the-art, next-generation sequencing to discover and target important variants within tumors.

  • Genomic prognostic test for patients newly diagnosed with early-stage, estrogen-receptor-positive, HER2-negative breast cancer.

  • Prolaris® is a molecular diagnostic test that helps determine the aggressiveness of a prostate cancer tumor to guide the best treatment decisions for prostate cancer patients.

  • HRD Status

    The most comprehensive FDA-approved tumor test that determines HRD status in women with ovarian cancer.

  • FDA-approved germline companion diagnostic test for patients with breast, ovarian, pancreatic and prostate cancer.

  • IHC Stains

    FDA-approved assay to identify patients with ovarian cancer who may qualify for treatment with mirvetuximab*

  • Offered together with Precise Tumor to measure protein expression and identify patients who may benefit from immunotherapy

Previous Test
    Next Test

    Affordable genetic testing

    Excellent insurance coverage

    Many patients pay $0 for genetic testing.

    Clear cost estimates

    Patients will know what their costs are—if any—before the test is run.

    Financial assistance

    Myriad offers assistance to manage out-of-pocket costs as well as a direct pay option.

    Latest research and publications

    Groundbreaking research to support patient health

    Myriad conducts industry-leading, innovative genetic research and testing to further the science of care. Our scientific studies have been published in prominent journals and at global conferences and feature breakthrough insights for improved patient treatments and outcomes.

    See our publications

    Get started with Myriad Oncology

    Request more information from our team.

    [email protected]

    (800) 469-7423

    Request more information about how Myriad Oncology can benefit you/your patients.

    Get started with Myriad Oncology

    Request more information about how Myriad’s Oncology solutions can benefit you/your patients.


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    References:
    1. Gradishar W, et al. Clinical variant classification: a comparison of public databases and a commercial testing laboratory. The Oncologist. 2017; 22(7):797–803. doi: 10.1634/theoncologist.2016-0431
    2. Mundt E, et al. Driving Down the Rate of Variants of Uncertain Significance as the Myriad MyRisk® Multigene Panel Grows [White paper]. Myriad Genetics. Oct 2019.
    3. Internal data on file at Myriad Genetics, Inc

    Myriad Genetics, MyRisk, Precise Tumor, MyChoice, Prolaris, BRACAnalysis CDx, RiskScore, and their respective logos, are registered trademarks of Myriad Genetics, Inc. and its subsidiaries in the United States and other jurisdictions. EndoPredict and the EndoPredict logo are either trademarks or registered trademarks of Eurobio Scientific.