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Non-progression of cervical intraepithelial neoplasia estimated from population-screening data.
Non-progression and duration of preclinical neoplastic lesions of the cervix uteri were studied using screening data from a previously unscreened population, Maribo County, Denmark (1966-82). To estimate regression rates, the incidence of clinical cancer before the screening programme was related to...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222698/ https://www.ncbi.nlm.nih.gov/pubmed/9000609 |
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author | Bos, A. B. van Ballegooijen, M. van Oortmarssen, G. J. van Marle, M. E. Habbema, J. D. Lynge, E. |
author_facet | Bos, A. B. van Ballegooijen, M. van Oortmarssen, G. J. van Marle, M. E. Habbema, J. D. Lynge, E. |
author_sort | Bos, A. B. |
collection | PubMed |
description | Non-progression and duration of preclinical neoplastic lesions of the cervix uteri were studied using screening data from a previously unscreened population, Maribo County, Denmark (1966-82). To estimate regression rates, the incidence of clinical cancer before the screening programme was related to the prevalence and incidence of preclinical lesions estimated from the detection rates of first smear and third and subsequent smears respectively. Duration was estimated from the time lag between the cumulative incidence of preclinical lesions and the combined cumulative incidence of clinical cancer and the estimated 'incidence of regression'. Of all preclinical lesions in women aged 25-50, 24% progressed, 39% regressed and 38% remained. Even if we assume no onset of preclinical lesions above age 50, we estimated that 48% of the preclinical lesions would not progress to clinical cancer in the women's lifetime. The estimated mean duration of preclinical lesions was 16 years. In Maribo County during the 1970s, the positive rate (1.6%) was low compared with current rates in several countries. We conclude that the detection of non-progressive lesions was outweighed by the prevention of clinical cancer. IMAGES: |
format | Text |
id | pubmed-2222698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22226982009-09-10 Non-progression of cervical intraepithelial neoplasia estimated from population-screening data. Bos, A. B. van Ballegooijen, M. van Oortmarssen, G. J. van Marle, M. E. Habbema, J. D. Lynge, E. Br J Cancer Research Article Non-progression and duration of preclinical neoplastic lesions of the cervix uteri were studied using screening data from a previously unscreened population, Maribo County, Denmark (1966-82). To estimate regression rates, the incidence of clinical cancer before the screening programme was related to the prevalence and incidence of preclinical lesions estimated from the detection rates of first smear and third and subsequent smears respectively. Duration was estimated from the time lag between the cumulative incidence of preclinical lesions and the combined cumulative incidence of clinical cancer and the estimated 'incidence of regression'. Of all preclinical lesions in women aged 25-50, 24% progressed, 39% regressed and 38% remained. Even if we assume no onset of preclinical lesions above age 50, we estimated that 48% of the preclinical lesions would not progress to clinical cancer in the women's lifetime. The estimated mean duration of preclinical lesions was 16 years. In Maribo County during the 1970s, the positive rate (1.6%) was low compared with current rates in several countries. We conclude that the detection of non-progressive lesions was outweighed by the prevention of clinical cancer. IMAGES: Nature Publishing Group 1997 /pmc/articles/PMC2222698/ /pubmed/9000609 Text en 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 | Research Article Bos, A. B. van Ballegooijen, M. van Oortmarssen, G. J. van Marle, M. E. Habbema, J. D. Lynge, E. Non-progression of cervical intraepithelial neoplasia estimated from population-screening data. |
title | Non-progression of cervical intraepithelial neoplasia estimated from population-screening data. |
title_full | Non-progression of cervical intraepithelial neoplasia estimated from population-screening data. |
title_fullStr | Non-progression of cervical intraepithelial neoplasia estimated from population-screening data. |
title_full_unstemmed | Non-progression of cervical intraepithelial neoplasia estimated from population-screening data. |
title_short | Non-progression of cervical intraepithelial neoplasia estimated from population-screening data. |
title_sort | non-progression of cervical intraepithelial neoplasia estimated from population-screening data. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2222698/ https://www.ncbi.nlm.nih.gov/pubmed/9000609 |
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