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HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3

The aim of this paper was to evaluate the factors that predict regression of untreated CIN 2 and 3. A total of 93 patients with colposcopic persistent CIN 2 and 3 lesions after biopsy were followed for 6 months. Human papillomavirus (HPV) types were determined by polymerase chain reaction at enrolme...

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Autores principales: Chan, J K, Monk, B J, Brewer, C, Keefe, K A, Osann, K, McMeekin, S, Rose, G S, Youssef, M, Wilczynski, S P, Meyskens, F L, Berman, M L
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376964/
https://www.ncbi.nlm.nih.gov/pubmed/12966426
http://dx.doi.org/10.1038/sj.bjc.6601196
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author Chan, J K
Monk, B J
Brewer, C
Keefe, K A
Osann, K
McMeekin, S
Rose, G S
Youssef, M
Wilczynski, S P
Meyskens, F L
Berman, M L
author_facet Chan, J K
Monk, B J
Brewer, C
Keefe, K A
Osann, K
McMeekin, S
Rose, G S
Youssef, M
Wilczynski, S P
Meyskens, F L
Berman, M L
author_sort Chan, J K
collection PubMed
description The aim of this paper was to evaluate the factors that predict regression of untreated CIN 2 and 3. A total of 93 patients with colposcopic persistent CIN 2 and 3 lesions after biopsy were followed for 6 months. Human papillomavirus (HPV) types were determined by polymerase chain reaction at enrolment. We analysed the biologic and demographic predictors of natural regression using univariate and multivariate methods. The overall regression rate was 52% (48 out of 93), including 58% (22 out of 38) of CIN 2 and 47% (26 out of 55) of CIN 3 lesions (P=0.31 for difference). Human papillomavirus was detected in 84% (78 out of 93) of patients. In univariate analysis, 80% (12 out of 15) of lesions without HPV regressed compared to 46% (36 out of 78) of lesions with HPV infection (P=0.016). Women without HPV and those who had a resolution of HPV had a four-fold higher chance of regression than those with persistent HPV (relative odds=3.5, 95% CI=1.4–8.6). Women with five or fewer lifetime sexual partners had higher rates of regression than women with more than five partners (P=0.003). In multivariate analysis, HPV status and number of sexual partners remained as significant independent predictors of regression. In conclusion, HPV status and number of lifetime sexual partners were strongly predictive of regression of untreated CIN 2 and 3.
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spelling pubmed-23769642009-09-10 HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3 Chan, J K Monk, B J Brewer, C Keefe, K A Osann, K McMeekin, S Rose, G S Youssef, M Wilczynski, S P Meyskens, F L Berman, M L Br J Cancer Molecular and Cellular Pathology The aim of this paper was to evaluate the factors that predict regression of untreated CIN 2 and 3. A total of 93 patients with colposcopic persistent CIN 2 and 3 lesions after biopsy were followed for 6 months. Human papillomavirus (HPV) types were determined by polymerase chain reaction at enrolment. We analysed the biologic and demographic predictors of natural regression using univariate and multivariate methods. The overall regression rate was 52% (48 out of 93), including 58% (22 out of 38) of CIN 2 and 47% (26 out of 55) of CIN 3 lesions (P=0.31 for difference). Human papillomavirus was detected in 84% (78 out of 93) of patients. In univariate analysis, 80% (12 out of 15) of lesions without HPV regressed compared to 46% (36 out of 78) of lesions with HPV infection (P=0.016). Women without HPV and those who had a resolution of HPV had a four-fold higher chance of regression than those with persistent HPV (relative odds=3.5, 95% CI=1.4–8.6). Women with five or fewer lifetime sexual partners had higher rates of regression than women with more than five partners (P=0.003). In multivariate analysis, HPV status and number of sexual partners remained as significant independent predictors of regression. In conclusion, HPV status and number of lifetime sexual partners were strongly predictive of regression of untreated CIN 2 and 3. Nature Publishing Group 2003-09-15 2003-09-09 /pmc/articles/PMC2376964/ /pubmed/12966426 http://dx.doi.org/10.1038/sj.bjc.6601196 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular and Cellular Pathology
Chan, J K
Monk, B J
Brewer, C
Keefe, K A
Osann, K
McMeekin, S
Rose, G S
Youssef, M
Wilczynski, S P
Meyskens, F L
Berman, M L
HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3
title HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3
title_full HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3
title_fullStr HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3
title_full_unstemmed HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3
title_short HPV infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of CIN 2 and 3
title_sort hpv infection and number of lifetime sexual partners are strong predictors for ‘natural’ regression of cin 2 and 3
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376964/
https://www.ncbi.nlm.nih.gov/pubmed/12966426
http://dx.doi.org/10.1038/sj.bjc.6601196
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