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HPV Virus Test May Improve
Cervical Cancer Detection

12-5-3


NEW YORK (Reuters Health) - Switching from Pap smears to human papillomavirus (HPV) testing as the primary screening method for cervical cancer could improve detection rates, a research team suggests. They also say that, with appropriate repeat screening, this strategy would not increase rates of referral for more invasive tests, which can sometimes be unnecessary.
 
In the current of The Lancet, Dr. J. Cuzick, at the Cancer Research UK in London, and associates outline a screening approach in which women would first be screened for HPV, a virus associated with the majority of cervical cancers, and those testing positive would then have a Pap test.
 
But "for HPV testing to be cost effective in primary screening, it would be necessary to develop an efficient policy for the management of women who test positive for high-risk HPV types," but have negative or borderline results on Pap screening, the team points out.
 
To explore the possible approaches for cervical cancer screening, the investigators studied 10,358 women, ages 30 to 60, who underwent cervical tissue testing (Pap smears) and who also had an HPV test.
 
Overall, HPV testing was more sensitive than Pap tests (97.1 percent vs. 76.6 percent) in detecting precancerous cervical tissues. The rate of false-positive tests was slightly higher with HPV testing than with Pap tests.
 
Among the study subjects, 825 women had borderline Pap results or positive high-risk HPV test results and negative Pap results.
 
Of this subgroup, 414 women were randomly assigned to undergo more extensive cervical tissue removal (colposcopy) and 411 women were assigned to have repeat HPV and Pap testing after 12 months (411 women) and then undergo colposcopy if needed. Low-risk and high-risk cervical tissue was identified in 7 percent and 3 percent of those who had immediate colposcopy, versus 4 percent and 2 percent in the surveillance group.
 
Thus, the researchers deduce, "surveillance at 12 months was as effective as immediate colposcopy."
 
Their findings suggest that women who had borderline Pap test results and negative HPV tests could have been safely returned to routine screening every three to five years without the need for additional follow-up.
 
In a related editorial in The Lancet, Dr. Eduardo L. Franco calls for further studies to define the duration of protection conferred by a negative HPV result and the effectiveness of using Pap smears as a second screening test.
 
Dr. Franco, from McGill University in Montreal, points out that a cervical cancer screening program that focuses on HPV, a sexually transmitted infection, will place "the emphasis of prevention not only on women but on their partners as well."
 
SOURCE: The Lancet, December 6, 2003.
 

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