MEDICATIONS: THREE-YEAR CERVICAL CANCER
SCREENING RECOMMENDATIONS MAY BE APPLICABLE FOR CERTAIN WOMEN WITH HIV
March 22, 2005 — Women with human immunodeficiency virus (HIV) who have
normal cervical cancer screening results and negative tests for human papilloma
virus (HPV), a sexually transmitted virus that is associated with cervical
cancer, may be able to have Papanicolaou (Pap) smears every three years, the
same interval as HIV-negative women, according to a study in the March 23/30
issue of the Journal of the American Medical Association.
According to background information in the article, "cervical cancer
screening recommendations in the United States have been recently updated and
now advise using an interval of three years between screenings in healthy women
30 years or older who have normal cytology (cells) results and who test negative
for oncogenic (cancer-associated) human papilloma virus (HPV) DNA. The
recommended interval is six to 12 months for women with normal cytology and
detectable oncogenic HPV." Women who are HIV-positive are recommended to have
two Pap smears six-months apart after their initial HIV diagnosis, and if both
are normal, should undergo an annual screening. HPV test results are not
considered.
Tiffany G. Harris, Ph.D., from Albert Einstein College of Medicine, Bronx,
N.Y., and colleagues studied the incidence of cervical squamous intraepithelial
lesions (SILs) [abnormal lesions] among HIV-seropositive (n= 855) and
HIV-seronegative (n= 343) who were enrolled in the Women's Interagency HIV Study
(WIHS) and had normal cervical cytology at the beginning of the study. The
researchers sought to determine if a single initial HPV test result could be
used to determine the appropriate cervical cancer screening interval in an
HIV-seropositive woman with normal cervical cytology.
The researchers found that after two years, "there were no large or
significant absolute differences in the cumulative incidence of SIL" between the
two groups of women. "In this observational cohort study, HIV-seronegative and
HIV-seropositive women who had normal cytology results with CD4 (cell) counts
greater than 500/microlitre and who had negative test results for HPV at
baseline had a similar low cumulative incidence of any SIL for three years or
more," the researchers report.
In conclusion the authors write: "Consideration will also need to be given to
the psychosocial costs of a positive HPV test in HIV-seropositive women, many of
whom will not develop SIL. However, according to the results of our study, we
believe that the use of HPV testing in HIV-seropositive women warrants
evaluation in a formal clinical trial."
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