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New ‘Super Test’ for Prostate Cancer Developed in the UK by EDX Medical

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CAMBRIDGE, England, February 17, 2025--(BUSINESS WIRE)--Scientists in Cambridge have developed a new ‘super test’ for prostate cancer in an effort to revolutionise screening and diagnosis of the disease and accelerate personalised treatment for patients.

The test identifies the presence or absence of cancerous cells, signs of early and late-stage cancer, whether it is slow or aggressive as well as genetic and hereditary risks in the patient.

The new test involves studying the most comprehensive combination of clinically-validated prostate-related biomarkers currently known, in both blood and urine samples. The interpretation of these biomarkers using a proprietary AI-driven algorithm highlights early signs of cancer and characteristic features that can guide treatment selection.

There are 55,000 new cases of prostate cancer in the UK each year, more than 330,000 across European Union countries and more than one million men undergoing treatment at any one time.

More than 100 clinically validated biomarkers are measured in the new test – which has been developed by EDX Medical Group plc. The biomarkers used in the test are then analysed by the specially created AI-powered algorithm which produces a detailed report of results for doctors. Currently available advanced tests which rely on up to 20 biomarkers per test.

EDX Medical scientists expect the test to consistently deliver exceptionally high accuracy with levels of sensitivity and specificity of between 96-99% across an extended age-range and diverse ethnic groups. By comparison, current standard of care prostate testing, including prostate specific antigen (PSA) tests and biopsies, can be below 50%.

The non-invasive ‘super test’ will detect various sub-types of prostate cancer determining key features particularly important for patients in non-caucasian higher risk groups.

The super test takes a ‘multi-omics’ approach and comprises a combination of multiple proteomic, transcriptomic, genetic/hereditary and epigenetic biomarker signatures which provide detailed biological data. A comprehensive list of phenotypic and symptom data is added to the biomarker data and is simultaneously analysed by the AI algorithm.

Individually, these biomarkers have all been clinically validated and published and in previous trials on more than 31,000 positive prostate cancer samples as well as more than 100,000 control non-cancer samples.

A highly accurate prostate cancer test will provide significant benefits for seemingly well 45-70 year-old men and also for healthcare providers. The increased accuracy should reduce the requirement to run unnecessary MRI scans. The need for highly invasive digital rectal examinations (DRE) will also be dramatically reduced.