Researchers may have invented a new, improved method to test for the most severe and bold shapes of prostate cancer. A new study, printed in JAMA Oncology on April 18, presented the MyProstateScore 2.0 (MPS2) test. MPS2 is a urine test that stretches for 18 individual genes linked to high-grade prostate cancer.

Prostate cancers are assigned a “step” from one to five established on how likely they are to quickly grow and spread. The MPS2 test may be able to pinpoint prostate cancers that satisfy the standards for quality group two or more increased, which are more difficult.

The power to notice whether an individual’s prostate cancer is low-grade (and less of a problem) or high-grade (and more of a concern) would help physicians filter out prostate cancer patients that don’t necessitate quick biopsy or intervention.

“Being capable of reducing the number of unneeded biopsies would be very useful because they can occasionally be sad, cause bleeding, and most notably, there is a slight chance of severe disease,” said Mark Katz, MD, clinical associate instructor of urology at the Boston University Chobanian and Avedisian School of Medicine.

Beyond just the physical, the MPS2 test could also deliver ease of mind for men with low-grade prostate cancer, who might otherwise face extreme pressure, doctor’s visits, and policies, Katz told Health.

Here’s what professionals had to say about the new trial, and how it piles up against other prostate cancer testing procedures.

How Does the MPS2 Exam Work?

Almost a decade ago, the same University of Michigan-based analysis team after MPS2 created an original interpretation of the urine test, anointed MPS. That earlier test read two other genes associated with prostate cancer, as well as an individual’s prostate-specific antigen (PSA) levels. 

But MPS2 improves upon the original version, explained study author Arul Chinnaiyan, MD, PhD, director of the Michigan Center for Translational Pathology at the University of Michigan Medical School.

“MPS—understanding 1—and some of the other retail urine and blood biomarkers for prostate cancer care to do well in seeing all conditions of prostate cancer, but small so in seeing high-grade, [grade group two], prostate cancer from those with low grade, [grade group one], indolent condition,” Chinnaiyan told Health. “[MPS2] is only to the other difficulties in seeing high-grade prostate cancer.”

PSA levels or other abnormal rectal exam results.

While creating this new test, Chinnaiyan and his group examined urine specimens from men who had advanced PSA levels or other abnormal rectal exam results.

Students used data from a product cohort—which had 761 men with a middle age of 63 to pick out the exact 18 genes that may be telling of higher-grade prostate cancer.

The 18-gene test was then used on a confirmation cohort of 743 men, where the analysis authors examined whether MPS2 could remember those men with quality group two or more increased cancers. Those effects revealed that the elevated test was “more useful at determining the medium and high-grade prostate cancers that need therapy,” Katz explained.

“Across a people of patients, the test contains about 40% of unneeded biopsies,” Chinnaiyan presented. “The trial works even reasonably in patients that have had a prior adverse biopsy, and can contain upwards of 50% of unneeded biopsies in this group.”

Of course, this new urine test could allow physicians to determine whether a patient with elevated PSA levels needs further intervention, said Katz.

How Does MPS2 Compare to Other Testing Strategies?

The most typical form of prostate cancer screening is the PSA blood test, Haywood said.

Because of this, students have been looking for ways to further determine a person’s actual risk of prostate cancer after they bring a PSA test, Haywood said.

“As a lot, we have been attempting to find more detailed features to enable better screenmen and decrease over-utilization of more active [or] invasive testing,” he counted.

One possibility is for physicians to use an MRI to also evaluate males with high PSA classes, Haywood said. Yet, he cautioned, these scans can sometimes miss positive cases and can be expensive and hard to access.

The Test Is Unrestricted, But More Research Is Needed

Though the study’s results are pledging, some rules and questions remain.

For one, there was little racial variety in the study people pool, and the study writers mentioned it’s not yet clear whether the results would be other in Black Americans.

This is especially important because there are “some public distinctions” when it comes to prostate cancers seen in Black and white patient residents, Chinnaiyan said. Especially, Black men present with prostate cancer before, have more bold cases, and have more increased mortality speeds than white men.

“By having 18 biomarkers, we wish to mitigate those differences,” he said. “That said, a future ongoing investigation will formally test MPS2 in a considerable African American cohort to ensure its implementation further.”

The longing is that the MPS2 test would “bear also across all racial levels,” Haywood said, but at this point, there just isn’t data to back it up.

In complement to testing MPS2 in Black Americans, Chinnaiyan stated he and his associates will also be glancing at the use of this test “in the active management people.” They want to see if MPS2 can “predict which patients have feisty prostate cancer, or whose cancer has gone.”

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