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Early human papillomavirus testing predicts residual/recurrent disease after LEEP
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 (CI...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Gynecologic Oncology and Colposcopy
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469856/ https://www.ncbi.nlm.nih.gov/pubmed/23094124 http://dx.doi.org/10.3802/jgo.2012.23.4.217 |
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author | Ryu, Aeli Nam, Kyehyun Kwak, Jeongja Kim, Jeongsig Jeon, Seob |
author_facet | Ryu, Aeli Nam, Kyehyun Kwak, Jeongja Kim, Jeongsig Jeon, Seob |
author_sort | Ryu, Aeli |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3469856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korean Society of Gynecologic Oncology and Colposcopy |
record_format | MEDLINE/PubMed |
spelling | pubmed-34698562012-10-23 Early human papillomavirus testing predicts residual/recurrent disease after LEEP Ryu, Aeli Nam, Kyehyun Kwak, Jeongja Kim, Jeongsig Jeon, Seob J Gynecol Oncol Original Article 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. Korean Society of Gynecologic Oncology and Colposcopy 2012-10 2012-09-19 /pmc/articles/PMC3469856/ /pubmed/23094124 http://dx.doi.org/10.3802/jgo.2012.23.4.217 Text en Copyright © 2012. Asian Society of Gynecologic Oncology, Korean Society of Gynecologic Oncology http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ryu, Aeli Nam, Kyehyun Kwak, Jeongja Kim, Jeongsig Jeon, Seob Early human papillomavirus testing predicts residual/recurrent disease after LEEP |
title | Early human papillomavirus testing predicts residual/recurrent disease after LEEP |
title_full | Early human papillomavirus testing predicts residual/recurrent disease after LEEP |
title_fullStr | Early human papillomavirus testing predicts residual/recurrent disease after LEEP |
title_full_unstemmed | Early human papillomavirus testing predicts residual/recurrent disease after LEEP |
title_short | Early human papillomavirus testing predicts residual/recurrent disease after LEEP |
title_sort | early human papillomavirus testing predicts residual/recurrent disease after leep |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469856/ https://www.ncbi.nlm.nih.gov/pubmed/23094124 http://dx.doi.org/10.3802/jgo.2012.23.4.217 |
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