Lynx Dx has commercially launched MyProstateScore 2.0 (MPS2), a urine test kit for prostate cancer intended for at-home sample collection by patients.
The test can be ordered by physicians and is now qualified for Medicare reimbursement.
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MPS2 analyses a comprehensive set of 18 gene transcripts to predict the presence of clinically significant prostate cancer.
Lynx Dx has developed the algorithm for “optimising” diagnostic accuracy and offering clinical flexibility, enabling the test to be used with or without including clinical risk factors, based on the preference of the physician.
MPS2 can be used by patients to test either in their own homes or at a medical facility.
This flexibility aligns the test with telehealth practices and expands access for individuals in remote or underserved areas. Moreover, the urine samples remain stable without the need for temperature control, stated the company.
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By GlobalDataAccording to the company, recent research has demonstrated that MPS2 delivered “high” accuracy in predicting clinically significant prostate cancer risk.
The study showed that MPS2 “outperformed” traditional prostate-specific antigen (PSA) testing, identifying up to 53% of men who would have an unnecessary biopsy, while keeping 91%–94% sensitivity for detecting high-grade cancer.
Lynx Dx chief medical officer Spencer Heaton said: “Giving patients the option to take the test at home, without the need to schedule a visit to the doctor or have a DRE, adds convenience, removes stigma and broadens access to a powerful method of screening for a serious disease.
“MyProstateScore 2.0 offers more clarity about the need for a biopsy in a way that aligns seamlessly with modern clinical workflows.”
Lynx Dx provides diagnostic testing services while leveraging technology from the University of Michigan. The company focuses on developing genomic tests especially where there is a significant need.
