A groundbreaking blood test developed by Test for Cancer can detect cancer up to 18 months before any symptoms show. The HrC Genomics blood test offers a non-invasive method to identify cancer early, potentially saving lives by catching the disease well before traditional diagnoses are possible.
Cancer remains one of the leading causes of death worldwide, and early detection is crucial for improving treatment outcomes. Unfortunately, many cancers are often found too late, limiting treatment options and lowering survival rates.
The HrC Genomics test changes this by detecting specific stem cells called pluripotent progenitor stem cells, which begin to circulate in the bloodstream when cancer develops—often 12 to 18 months prior to any symptoms. By spotting these early markers, the test provides a valuable window of opportunity for timely medical intervention.
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Unlike many screening tools, this test is available to adults of all ages, regardless of gender or family history. This accessibility opens the door for wider cancer screening and early detection, even for individuals who may not qualify for conventional screenings.
Test for Cancer is committed to making early cancer detection broadly accessible, empowering more people to take proactive steps toward their health and improving the chances of successful treatment by catching cancer in its earliest stages.