Genomic tests for prostate cancer help assess risk, guide treatment, and predict disease progression.

‘#Genomictests are helping doctors better understand how aggressive #prostatecancer can be, even in low-risk cases. This could lead to more personalized treatment plans. ’

What the Study Found:
Observational studies with low bias showed most patients with very low or low baseline risk retained their risk category, though reclassification rates varied by test: 88.1%-100% for GPS, 82.9%-87.2% for Decipher and 76.9% for Prolaris. A randomized trial, however, reported higher reclassification rates to elevated risk categories (34.5% for very low risk and 29.4% for low risk with GPS). 




For intermediate-risk patients, upward or downward reclassification depended on the genomic test. GPS studies reported minimal upward reclassification (0%-1.7%) but higher rates of downward reclassification (3.8%-28.8%). Decipher and Prolaris studies showed more substantial risk reclassification in both directions.
Race also influenced reclassification patterns, with differences observed in Black and white men.
Treatment decisions after testing often shifted toward active surveillance in observational studies, while randomized trials found GPS testing slightly increased preferences for removal of a cancerous prostate gland or radiation.
“Genomic tests give us a clearer picture of how aggressive prostate cancer might be,” said Amir Alishahi Tabriz, M.D., Ph.D., assistant member in the Department of Health Outcomes and Behavior at Moffitt and lead author of the review. “While these tests show promise, we need more well-designed studies to see exactly how they can improve treatment for patients. This is an exciting area of research for the future of cancer care.”
Advertisement
Source-Eurekalert