New ACOG Practice Bulletin Recognizes Value of HPV Screeening in Its Highest Level of Recommendation
4/17/2005 Gaithersburg, MD press release PRSNewswire HPV DNA testing is 'more sensitive than cervical cytology' in detecting high grade cervical disease A newly released Practice Bulletin from the American College of Obstetricians and Gynecologists (ACOG) recognizes testing for the human papillomavirus (HPV) as "more sensitive than cervical cytology [the Pap test]" for detection of pre- cancerous cells (CIN 2/3) and cervical cancer. Digene is the developer of the only FDA-approved test for high-risk types of HPV, the cause of virtually all cases of cervical cancer. The Digene HPV Test, also marketed as the DNAwithPap(TM) Test, is approved for use in conjunction with a Pap test for women age 30 and older. ACOG's April 2005 Practice Bulletin on HPV summarizes epidemiology and transmission of the virus, discusses the incorporation of HPV screening into clinical practice, and provides guidance on how to use the test results to tailor patient management. ACOG represents more than 45,000 physicians who provide health care for women. The bulletin concludes, as a "Level A" recommendation "based on good and consistent scientific evidence," that HPV testing together with a Pap test is more sensitive in detecting cancer than a Pap test alone: * "Because HPV DNA testing is more sensitive than cervical cytology in detecting CIN 2 and CIN 3, women with negative concurrent test results can be reassured that their risk of unidentified CIN 2 and CIN 3 or cervical cancer is approximately 1 in 1,000." * "Studies using combined HPV testing with cervical cytology have reported [...]