Take the next step with Prolaris

Navigate crucial prostate cancer treatment decisions – with the right answers at the right time.

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Prolaris®
Prostate Cancer Prognostic Test

His options just became clearer

When you want to bring clarity and personalization to your prostate cancer treatment discussions, go beyond risk stratification at biopsy with Prolaris testing.

The patient in front of you wants to know more

Patients want to be confident that their doctors treatment recommendation is THEIR best option. Prolaris delivers a personalized risk assessment of a patient’s prostate cancer by combining clinically proven information with traditional diagnostic tools like PSA and Gleason.

45%

of biopsy and surgical Gleason scores do not match.1

34%

of the time, expert-trained GU pathologists disagree about biopsy Gleason scores.2

plays 'Improving the patient experience through genomics' videolightbox

Improving the patient experience through genomics

The Prolaris test is the most comprehensive test available

When it comes to making active surveillance or definitive treatment decisions, selecting the correct biomarker test matters. Prolaris is the only test studied in untreated patients and can identify the MOST patients for active surveillance across all biomarkers.4

The Prolaris test combines genomic (CCP) and clin-path features. CCP is the gold standard for measuring cancer aggressiveness.

The Prolaris test is validated in 10,000 patients across all risk groups.3

Prolaris is two times more prognostic than PSA/Gleason alone8


clinical variables graphic

Independent is good, but comprehensive is better

Prolaris has an independent CCP score that determines cancer aggressiveness and is combined with more traditional clinical pathological features like PSA and Gleason to create the most prognostic test on the market.

Go Beyond Risk Stratification at Biopsy

Prolaris can identify which men are safe for active surveillance and those who are not. With two clinically validated thresholds, Prolaris can also identify which patients should consider actively treating their cancer with one form of treatment, like surgery or radiation, and which patients will benefit from multiple forms of treatment

Active surveillance

Identify active surveillance (AS) patients at time of biopsy

Because the Prolaris® test was developed and validated on untreated men,4 AS conversations with the untreated patient in front of you are more relevant and informed.

The Prolaris test outperforms all other biomarkers in identifying the right patients for active surveillance in both low and intermediate risk populations4

In the Prolaris validation study, NO patient below the AS threshold died of prostate cancer4

The Prolaris biomarker best aligns with patients studied in ProtecT, the largest randomized trial of AS or treatment in screen-detected localized prostate cancer5

Single-modal Treatment

Identify the patients who need definitive treatment and at what intensity

The Prolaris® test shows that those patients who fall below the multi-modal threshold do not benefit from intensifying treatment6

Establishing the multi-modal threshold

The Prolaris test threshold was developed on approximately 1,500 intermediate and high-risk patients from two separate cohorts

Validating patients prior to a multi-modal treatment

Patients were separated by those who received single-modal therapy versus those with multiple modes of treatment

Multi-modal Threshold

Guide the androgen deprivation therapy (ADT) conversation

Multiple groups with ADT variations evaluated for metastasis

The Multi-modal threshold was developed and double-validated across all outcomes to predict the risk of metastasis and determine which patients can safely forego ADT6,7

At or below the multi-modal threshold
(8.8% metastasis risk)

The Prolaris® test gives your patients personalized, shareable guidance and a simple “number-needed-to-treat” value

Is ADT right for this patient?

With the Prolaris test, there’s nothing to decipher

2x the predictive power of PSA and Gleason combined8

Outperforms all other biomarkers in active surveillance9

Only test developed and validated on untreated men4

Most comprehensive: combines genomic, PSA and Gleason scores8

Goes beyond risk stratification to determine which patients need treatment and the appropriate level of intensity

Personalizes ADT decisions with ARR for every patient

For you and the patient in front of you, when it comes to finding the best tool to bring clarity, utility and personalization to your prostate cancer treatment discussions, the conversation just got easier.

plays 'The clinical utility of Prolaris in prostate cancer' videolightbox

The clinical utility of Prolaris® in prostate cancer

plays 'Prolaris empowers clinicians during a cancer consult' videolightbox

Prolaris® empowers clinicians during a cancer consult

Meet Myriad UroSuite

The complete suite of tests for a full prostate cancer workup.

Myriad UroSuite gives healthcare providers the ability to directly order a complete suite of tests – including biomarker, germline, and somatic – for clear, comprehensive insights to guide prostate cancer treatment.

What to expect with every Prolaris test

Actionable

Every Prolaris test provides actionable results to inform more confident prostate cancer treatment decisions.

Affordable

Myriad is committed to providing patients with access to accurate and affordable genetic results through extensive coverage with most insurance plans and financial assistance programs.

Accurate

Myriad believes in providing the most accurate and highest quality tests for patients. From hereditary cancer to precision medicine, our tests are designed to give providers and patients the most accurate answer possible.

Prolaris resources

References:

  1. Schreiber D, Wong AT, Rineer J, Weedon J, Schwartz D. Prostate biopsy concordance in a large population-based sample: a Surveillance, Epidemiology and End Results study. J. Clin. Path. 2015;68(6):453-457. doi:https://doi.org/10.1136/jclinpath-2014-202767.
  2. Allsbrook WC, Mangold KA, Johnson MH, et al. Interobserver reproducibility of Gleason grading of prostatic carcinoma: Urologic pathologists. Hum. Pathol. 2001;32(1):74-80. doi:https://doi.org/10.1053/hupa.2001.21134
  3. https://prolaris.com/posters-and-medical-publications/#!#home.
  4. Lin DW, E. David Crawford, 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. doi:https://doi.org/10.1016/j.urolonc.2018.03.011.
  5. Hamdy FC, Donovan JL, Lane JA, et al. Fifteen-Year Outcomes after Monitoring, Surgery, or Radiotherapy for Prostate Cancer. NEJM. Published online March 11, 2023. doi:https://doi.org/10.1056/nejmoa2214122.
  6. Tward J, Lenz L, Flake DD, et al. The Clinical Cell-Cycle Risk (CCR) Score Is Associated With Metastasis After Radiation Therapy and Provides Guidance on When to Forgo Combined Androgen Deprivation Therapy With Dose-Escalated Radiation. IJROBP. 2022;113(1):66-76. doi:https://doi.org/10.1016/j.ijrobp.2021.09.034.
  7. Tward JD, Schlomm T, Bardot S, et al. Ability of the combined clinical cell-cycle risk score to identify patients that benefit from multi versus single modality therapy in NCCN intermediate and high-risk prostate cancer. J. Clin. Onc. 2020;38(6_suppl):346-346. doi:https://doi.org/10.1200/jco.2020.38.6_suppl.346.
  8. Cuzick J, Berney DM, Fisher G, et al. Prognostic value of a cell cycle progression signature for prostate cancer death in a conservatively managed needle biopsy cohort. Br. J. Cancer. 2012;106(6):1095-1099. doi:https://doi.org/10.1038/bjc.2012.39.
  9. 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):1-15. doi:https://doi.org/10.1200/po.18.00163.