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Identifying Women With Cervical Neoplasia: Using Human Papillomavirus DNA Testing for Equivocal Papanicolaou Results
CONTEXT A Papanicolaou (Pap) test result of atypical squamous cells of undetermined significance (ASCUS) presents a clinical challenge. Only 5% to 10% of women with ASCUS harbor serious cervical disease, but more than one third of the high-grade squamous intraepithelial lesions (HSILs) in screening...
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Published in: | JAMA : the journal of the American Medical Association 1999-05, Vol.281 (17), p.1605-1610 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | CONTEXT A Papanicolaou (Pap) test result of atypical squamous
cells of undetermined significance (ASCUS) presents a clinical
challenge. Only 5% to 10% of women with ASCUS harbor serious cervical
disease, but more than one third of the high-grade squamous
intraepithelial lesions (HSILs) in screening populations are identified
from ASCUS Pap test results. OBJECTIVE To determine whether human papillomavirus (HPV) DNA
testing of residual material from liquid-based Pap tests and referral
of cases found to be HPV-positive directly to colposcopy could provide
sensitive detection of underlying HSILs in women with ASCUS Pap
results, compared with repeat Pap testing. DESIGN AND SETTING Natural history of women with ASCUS Pap smear
results, all of whom had liquid-based cytology, HPV testing, and
subsequent repeat Pap tests and colposcopy with histologic evaluation,
conducted at 12 gynecology clinics in a large managed care organization
between October 1995 and June 1996. PARTICIPANTS From a cohort of 46,009 women who had
routine cervical examinations, 995 women with Pap test results of ASCUS
who consented to participate were identified. MAIN OUTCOME MEASURES Cervical histology, HPV test
results, and repeat Pap smear results, and sensitivity of HPV testing
to identify patients found to have HSIL+ histology. RESULTS Of 995 participants with ASCUS Pap test results, 973 had
both a definitive histologic diagnosis and HPV result. Sixty-five
(6.7%) had histologic HSIL or cancer. For women with histologic HSIL+,
the HPV test was positive in 89.2% (95% confidence interval [CI],
78.4%-95.2%), and the specificity was 64.1% (95% CI,
60.9%-67.2%). The repeat Pap smear result was abnormal in 76.2%
(95% CI, 63.5%-85.7%). Triage based on HPV testing only or on repeat
Pap testing only would refer similar proportions (approximately 39%)
to colposcopy. The sensitivity of HPV DNA testing for HSIL was
equivalent to, if not greater than, that of the repeat Pap test. We
further estimated that an HPV-based algorithm including the immediate
colposcopy of HPV-positive women, and then repeat Pap testing of all
others, would provide an overall sensitivity of 96.9% (95% CI,
88.3%-99.5%). CONCLUSIONS For women with ASCUS Pap tests, HPV DNA testing of
residual specimens collected for routine cervical cytology can help
identify those who have underlying HSIL. By testing the specimen
collected at initial screening, the majority of high-risk cases can be
identified and referred for colposcopy based o |
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ISSN: | 0098-7484 1538-3598 |
DOI: | 10.1001/jama.281.17.1605 |