Overview

The Prostatype test was developed by Prostatype Genomics after more than 15 years of research and is offered by Cambridge Clinical Laboratories. It is a genomic test that assesses how aggressive prostate cancer is. It guides whether immediate treatment is needed or if active surveillance is appropriate.



How it Works

  • Analyzes three stem-cell mRNA biomarkers (F3, IGFBP3, VGLL3) from existing biopsy samples. No new biopsy required.

  • Combines biomarker data with PSA levels, Gleason score, tumour stage, and clinical information.

  • Generates a P-score, indicating 10-year risk of death from prostate cancer without treatment.


  • Accuracy

  • Outperforms traditional models (D’Amico and CAPRA) in predicting prostate cancer mortality.

  • Enables 35% of patients to be safely reclassified to active surveillance, while confirming treatment for 65%.

  • P-score has a high prognostic accuracy (AUC ~0.89) and strong correlation with 10-year cancer-specific mortality (hazard ratio ~1.6).


  • Benefits

  • Reduces overtreatment and undertreatment.

  • Supports better-informed treatment decisions.

  • Offers cost-efficient and scalable use through existing biopsy materials.


  • Eligibility

  • Suitable for newly diagnosed patients who need clarity on cancer aggressiveness.

  • Also available for patients under active surveillance. Requires a more recent biopsy sample.

  • Access via private specialist consultants. Some named consultants currently offering it:

    • Tim Dudderidge (Spire Southampton)

    • Jaimin Bhatt (Ross Hall Clinic, Glasgow)

    • Utsav Reddy (Spire Norwich)

  • NHS patients must access Prostatype through private consultation, either via their NHS consultant offering private services or arranged through Prostatype’s facilitators.

  • Get your Prostatype test

    Prostatype offers men with prostate cancer a clearer picture of how aggressive their disease is, helping avoid both overtreatment and undertreatment.