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Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester

BACKGROUND: Long-term follow-up of large cohorts is needed to determine the effects of HPV and screening on CIN3 (grade 3 cervical intraepithelial neoplasia) and ICC (invasive cervical cancer). METHODS: Women were recruited when attending for routine cervical screening in Greater Manchester, UK: 198...

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Autores principales: Gilham, Clare, Sargent, Alexandra, Crosbie, Emma J., Peto, Julian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147679/
https://www.ncbi.nlm.nih.gov/pubmed/36959379
http://dx.doi.org/10.1038/s41416-023-02227-9
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author Gilham, Clare
Sargent, Alexandra
Crosbie, Emma J.
Peto, Julian
author_facet Gilham, Clare
Sargent, Alexandra
Crosbie, Emma J.
Peto, Julian
author_sort Gilham, Clare
collection PubMed
description BACKGROUND: Long-term follow-up of large cohorts is needed to determine the effects of HPV and screening on CIN3 (grade 3 cervical intraepithelial neoplasia) and ICC (invasive cervical cancer). METHODS: Women were recruited when attending for routine cervical screening in Greater Manchester, UK: 1987–93 for the Manchester Cohort (MC: 47,625 women) and 2001–03 for the ARTISTIC Cohort (AC: 24,496 women). Both were followed through national registration for cancer incidence and mortality to 2020. RESULTS: Risk patterns following HPV infection differed for CIN3 and ICC. Risk of ICC in the MC rises for 30 years following a single positive HPV test, reaching 2.5% (95% CI: 1.3–4.5%). A similar pattern was seen in the AC, but the risks of cancer were approximately halved. CIN3 was diagnosed much sooner in the AC due to more efficient cytology. More sensitive HPV testing was able to better predict future risk. CONCLUSION: The sensitivity of HPV testing and cytology influences the CIN3 detection rate. Sensitive HPV testing enables effective risk stratification. Increased risk of ICC is observed 15–30 years after HPV infection. Women testing HPV + should be followed until their infection clears. Discharging women from screening programmes whilst they remain HPV + may not be safe, even if cytology and colposcopy tests are normal.
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spelling pubmed-101476792023-04-30 Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester Gilham, Clare Sargent, Alexandra Crosbie, Emma J. Peto, Julian Br J Cancer Article BACKGROUND: Long-term follow-up of large cohorts is needed to determine the effects of HPV and screening on CIN3 (grade 3 cervical intraepithelial neoplasia) and ICC (invasive cervical cancer). METHODS: Women were recruited when attending for routine cervical screening in Greater Manchester, UK: 1987–93 for the Manchester Cohort (MC: 47,625 women) and 2001–03 for the ARTISTIC Cohort (AC: 24,496 women). Both were followed through national registration for cancer incidence and mortality to 2020. RESULTS: Risk patterns following HPV infection differed for CIN3 and ICC. Risk of ICC in the MC rises for 30 years following a single positive HPV test, reaching 2.5% (95% CI: 1.3–4.5%). A similar pattern was seen in the AC, but the risks of cancer were approximately halved. CIN3 was diagnosed much sooner in the AC due to more efficient cytology. More sensitive HPV testing was able to better predict future risk. CONCLUSION: The sensitivity of HPV testing and cytology influences the CIN3 detection rate. Sensitive HPV testing enables effective risk stratification. Increased risk of ICC is observed 15–30 years after HPV infection. Women testing HPV + should be followed until their infection clears. Discharging women from screening programmes whilst they remain HPV + may not be safe, even if cytology and colposcopy tests are normal. Nature Publishing Group UK 2023-03-23 2023-05-11 /pmc/articles/PMC10147679/ /pubmed/36959379 http://dx.doi.org/10.1038/s41416-023-02227-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access 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 http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gilham, Clare
Sargent, Alexandra
Crosbie, Emma J.
Peto, Julian
Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester
title Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester
title_full Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester
title_fullStr Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester
title_full_unstemmed Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester
title_short Long-term risks of invasive cervical cancer following HPV infection: follow-up of two screening cohorts in Manchester
title_sort long-term risks of invasive cervical cancer following hpv infection: follow-up of two screening cohorts in manchester
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147679/
https://www.ncbi.nlm.nih.gov/pubmed/36959379
http://dx.doi.org/10.1038/s41416-023-02227-9
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