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Early human papillomavirus testing predicts residual/recurrent disease after LEEP

Authors
Ryu, AeliNam, KyehyunKwak, JeongjaKim, JeongsigJeon, Seob
Issue Date
Oct-2012
Publisher
대한부인종양학회
Keywords
Cervical intraepithelial neoplasia; Follow-up; Human papillomavirus; Loop electrosurgical excision procedure
Citation
Journal of Gynecologic Oncology, v.23, no.4, pp 217 - 225
Pages
9
Journal Title
Journal of Gynecologic Oncology
Volume
23
Number
4
Start Page
217
End Page
225
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/14800
DOI
10.3802/jgo.2012.23.4.217
ISSN
2005-0380
2005-0399
Abstract
Objective: The purpose of this study was to determine the predictive factors for residual/recurrent disease and to analyze the timing for Pap smears and human papillomavirus (HPV) testing during follow-up after loop electrosurgical excision procedure (LEEP) for cervical intraepithelial neoplasia (CIN) 2 or worse. Methods: We retrospectively analyzed 183 patients (mean age, 39.3 years) with CIN 2/3 who were treated with LEEP. Post-LEEP follow-up was performed by Pap smear and HPV hybrid capture2 (HC2) testing. The definition of persistent/recurrent disease was biopsy-proven CIN 2 or worse. Results: Among 183 patients, punch biopsies were CIN 2 in 31 (16.9%) and CIN 3 in 152(83.1%). HPV HC2 tests before LEEP were positive in 170(95.5%) of 178 patients. During follow-up, 12 patients (6.6%) had residual/recurrent CIN 2+. LEEP margin status was a significant predictive factor for persistent/recurrent disease. Other factors such as age, HPV HC2 viral load (>= 100 relative light units), and HPV typing (type 16/18 vs. other types) did not predict recurrence. Early HPV HC2 testing at 3 months after LEEP detected all cases of residual/recurrent disease. The sensitivity and negative predictive value of the HPV HC2 test for residual/recurrent disease were both 100% at 3 and 6 months. Conclusion: Margin involvement in conization specimens was a significant factor predicting-residual/recurrent disease after LEEP. HPV test results at 3 and 6 months after treatment were comparable. Early 3-month follow-up testing after LEEP can offer timely information about residual/recurrent disease and alleviate patient anxiety early about treatment failure.
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