USPSTF Draft Cervical Cancer Screening Guidelines Could Bring Headwinds for Pap Test Providers

This article has been updated to clarify that Roche's HPV assay is the only one on the market with an FDA-approved primary screening indication, and not the only FDA-approved HPV test on the market.

NEW YORK (GenomeWeb) – The US Preventative Services Task Force has issued draft recommendations proposing that women in their 20s be screened for cervical cancer every three years with cervical cytology alone.