A less invasive option for watching low-risk prostate cancer
A new urine test may change how doctors monitor men with low-risk prostate cancer who are on active surveillance. According to a study published in The Journal of Urology, the test performed better than PSA-based testing and MRI in this setting and could have avoided up to 64% of unnecessary repeat biopsies while still detecting higher-grade cancers that warrant treatment.
The test, called MyProstateScore 2.0-Active Surveillance, or MPS2-AS, was evaluated in more than 300 patients with Grade Group 1 prostate cancer. The result addresses one of the most persistent burdens in active surveillance: the need for repeated prostate biopsies every two to three years because current noninvasive tools do not reliably rule out clinically important progression.
Why surveillance still feels invasive
Active surveillance is widely used because many low-risk prostate cancers are unlikely to cause harm if watched carefully rather than treated immediately. That approach helps patients avoid unnecessary surgery or radiation. But surveillance comes with its own costs. Some patients later prove to have higher-risk disease, so doctors must keep checking for signs of upgrading.
Because PSA testing and imaging have limits, repeat biopsy remains central to the current model. Biopsies can be uncomfortable, invasive, and anxiety-producing. A test that helps determine who really needs one, and who can safely avoid it, would therefore fill a major gap.
That is the problem MPS2-AS is trying to solve. Rather than replacing monitoring altogether, it aims to make monitoring more selective and more precise.







