GENOMIC AND GERMLINE TESTING WITH MYRIAD ONCOLOGY

Personalize prostate cancer management and treatment strategies

Myriad offers risk stratification and genomic tools that inform management decisions for every patient you treat, from newly diagnosed to advanced cancer.

Clinical utility across the prostate cancer care continuum

Gaining individualized genetic insights about your patient’s prostate cancer gives you valuable information that can help you decide on the best treatment plan for your patient, thereby improving patient outcomes.

Early-Stage & Treatment Selection

  • Active surveillance
  • Surgery
  • Radiation therapy
  • Adjuvant therapy


High-Risk & Metastatic Disease

  • Targeted therapy selection
  • Clinical trial eligibility




Prolaris® Prostate Cancer Prognostic Test. Built to personalize treatment decisions for low- and favorable intermediate-risk prostate cancer.

Patients with intermediate-risk prostate cancer often fall into the “gray zone,” where decisions between active surveillance and treatment can be difficult. The Prolaris Test was developed for untreated patients with localized prostate cancer providing clear answers to support treatment discussions for low and intermediate-risk patients.1 It outperforms all other biomarkers in identifying which patients may be appropriate to pursue active surveillance (AS).2

See how the Prolaris Test helped Marcus and his care team.

No prostate cancer patient deserves the intermediate risk “gray zone”

Combining the MyRisk® Hereditary Cancer Test and Precise Tumor® Molecular Profile Test reveals more for your patients with advanced prostate cancer.

Men with advanced prostate cancer may qualify for targeted treatments and clinical trials based on their germline and somatic mutation status.3 Combining germline and somatic testing doubles the chances of identifying clinically actionable mutations.4 That’s why clinical guidelines support combined testing:3

  • Germline testing for all patients with high-risk, very high-risk, regional, or metastatic prostate cancer (or any stage with family history suggestive of hereditary cancer)
  • Somatic tumor testing for metastatic prostate cancer to detect DNA repair gene mutations (e.g., BRCA1, BRCA2, ATM, etc.) relevant for PARP inhibitor eligibility and other targeted therapies

Germline testing with the MyRisk Test

Molecular profiling with the Precise Tumor Test

By ordering both tests from Myriad, you get consolidated, concordant results — avoiding the inconsistencies that arise when multiple labs interpret variants differently. Our integrated approach means clearer reporting, fewer redundancies, and greater confidence in distinguishing inherited from somatic mutations, helping you identify more patients for targeted therapies and clinical trials.

Genomic and germline insights for confident management across the prostate cancer care continuum

  • for newly diagnosed and untreated patients

    The Prolaris Test is a cell-cycle proliferation biomarker test combining clinical and pathological features with a personalized tumor aggressiveness score to help determine if a patient can safely stay on active surveillance or should pursue treatment.

  • for patients with high-risk to metastatic cancer

    The MyRisk Test is a guideline-driven germline test that identifies inherited mutations in genes like BRCA1 and others, to help determine eligibility for targeted therapies such as PARP inhibitors.3,5

  • for patients with metastatic disease

    A somatic test with broad coverage of guidelines that analyzes over 500 genes, as well as key biomarkers like MSI, TMB, and PD-L1, to determine eligibility for FDA-approved therapies and clinical trials.6

Previous Test
    Next Test

    Streamlined support for you and your 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 for the MyRisk Test, financial assistance, and other affordability options, including direct pay. A majority of patients face no out-of-pocket costs for the Prolaris Test.7

    Fast results

    Consolidated germline and tumor genomic results are available, on average, 14 days after our 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 Liaisons 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

    Streamlined support for you and your 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 for the MyRisk Test, financial assistance, and other affordability options, including direct pay. A majority of patients face no out-of-pocket costs for the Prolaris Test.7

    Fast results

    Consolidated germline and tumor genomic results are available, on average, 14 days after our 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 Liaisons 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

    Provider content and resources

    The Modern Urologist Podcast: Expert perspectives on precision medicine in urology

    Join leading voices in urology as they explore advances in prostate cancer genomics, evolving treatment guidelines, and the future of precision medicine.

    Provider Stories: Peer insights from using the Prolaris Test in practice

    Hear from fellow clinicians on how the Prolaris Test has changed the way they manage prostate cancer care — helping identify which patients can safely choose active surveillance and which may benefit from treatment.

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    Robert Jansen, Urologist
    South Carolina

    The latest Prolaris report has a great layout. I’m very happy with it. It’s important to me to be able to explain a test report to a patient.

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    David Rich, Urologist
    South Carolina

    I find the utility for Prolaris most helpful in the patients with low risk or immediate risk prostate cancer.

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    Tim Richardson, Urologist
    Kansas

    Prolaris is very helpful with preventing over treating in some of these patients, especially with the intensification of treatment.

    Additional resources

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    Myriad Oncology Solutions for advanced prostate cancer

    Combining germline and somatic testing empowers you to navigate complex decisions in advanced prostate cancer care.

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    Publications & posters

    Stay current with clinical validation and utility publications and more.

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    Documents & forms

    Find the Myriad documents and forms you need right here.

    References:
    1. Lin DW, Crawford ED, Keane T, et al. Identification of men with low-risk biopsy-confirmed prostate cancer as candidates for active surveillance. Urol Oncol. 2018;36(6):310.e7-310.e13.
    2. Hu JC, Tosoian JJ, Qi J, et al. Clinical Utility of Gene Expression Classifiers in Men With Newly Diagnosed Prostate Cancer. JCO Precis Oncol. 2018;2:PO.18.00163.
    3. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Prostate Cancer. V3.2026. © National Comprehensive Cancer Network, Inc. 2025. All rights reserved. Accessed November 11, 2025. To view the most recent and complete version of the guideline, visit NCCN.org. NCCN makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.
    4. Berchuck JE, Boiarsky D, Silver R, et al. Addition of Germline Testing to Tumor-Only Sequencing Improves Detection of Pathogenic Germline Variants in Men With Advanced Prostate Cancer. JCO Precis Oncol. 2022;6:e2200329.
    5. National Comprehensive Cancer Network (NCCN). NCCN Clinical Practice Guidelines in Oncology. Genetic /Familial High-Risk Assessment: Breast, Ovarian, Pancreatic, and Prostate. V2.2026. © National Comprehensive Cancer Network, Inc. 2025. All rights reserved. Accessed November 11, 2025. To view the most recent and complete version of the guideline, visit NCCN.org. NCCN makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.
    6. Conroy JM, Pabla S, Glenn ST, et al. A scalable high-throughput targeted next-generation sequencing assay for comprehensive genomic profiling of solid tumors. PLoS One. 2021;16(12):e0260089.
    7. Based on a review of 12 months of past claim data for major insurance carriers across the US, the majority of patients face no out-of-pocket costs for their Prolaris test. Last updated 2024.

    ©2026 Myriad Genetics, Myriad Oncology, MyRisk, Precise Tumor, Prolaris, and their respective logos, are either trademarks or registered trademarks of Myriad Genetics, Inc. and its subsidiaries in the United States and other jurisdictions.