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Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016

We analysed patterns in the incidence of cervical intraepithelial neoplasia grades 2 and 3 (CIN2, CIN3) and adenocarcinoma in situ (AIS) by age and histology in 1992–2016 in Norway and described changes in screening tests. Incident cases of CIN2, CIN3, AIS and cervical cancer were identified in the...

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Autores principales: Orumaa, Madleen, Leinonen, Maarit K, Campbell, Suzanne, Møller, Bjørn, Myklebust, Tor Åge, Nygård, Mari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767573/
https://www.ncbi.nlm.nih.gov/pubmed/30734284
http://dx.doi.org/10.1002/ijc.32195
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author Orumaa, Madleen
Leinonen, Maarit K
Campbell, Suzanne
Møller, Bjørn
Myklebust, Tor Åge
Nygård, Mari
author_facet Orumaa, Madleen
Leinonen, Maarit K
Campbell, Suzanne
Møller, Bjørn
Myklebust, Tor Åge
Nygård, Mari
author_sort Orumaa, Madleen
collection PubMed
description We analysed patterns in the incidence of cervical intraepithelial neoplasia grades 2 and 3 (CIN2, CIN3) and adenocarcinoma in situ (AIS) by age and histology in 1992–2016 in Norway and described changes in screening tests. Incident cases of CIN2, CIN3, AIS and cervical cancer were identified in the Cancer Registry of Norway, as were all women with at least one screening test. The annual percentage change statistic was used to assess point estimates and changes in age‐specific and age‐standardised incidence rates (IR). Women aged 25–29 years had the highest incidence of cervical precancerous lesions (CIN2: 192.9/10, CIN3: 737.2/10, AIS: 32.5/10(5) in 2016). The IR of CIN2 increased for all screening ages (25–69 years) from 3.6% to 6.7% per year. CIN3 incidence increased by 1.6% (95% confidence interval [CI] 0.6–2.6) annually. A steep increase in AIS incidence was observed in all age groups (7.1% per year, 95% CI 5.3–8.8). Changes in screening tests and the histological verification of cervical precancerous lesions alone cannot explain the steady increase in incidence we observed over the 25‐year study period, and increased exposure to human papillomavirus (HPV) likely plays a role. Age‐appropriate treatment of screening‐detected cervical precancerous lesions is needed for effective cervical cancer control while avoiding overtreatment and related health risks. In order to perform an appropriate harm‐benefit evaluation of cervical cancer control efforts, detailed information on screening technology and background risks, including HPV vaccination status, is needed to create optimal public health policy.
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spelling pubmed-67675732019-10-03 Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016 Orumaa, Madleen Leinonen, Maarit K Campbell, Suzanne Møller, Bjørn Myklebust, Tor Åge Nygård, Mari Int J Cancer Cancer Epidemiology We analysed patterns in the incidence of cervical intraepithelial neoplasia grades 2 and 3 (CIN2, CIN3) and adenocarcinoma in situ (AIS) by age and histology in 1992–2016 in Norway and described changes in screening tests. Incident cases of CIN2, CIN3, AIS and cervical cancer were identified in the Cancer Registry of Norway, as were all women with at least one screening test. The annual percentage change statistic was used to assess point estimates and changes in age‐specific and age‐standardised incidence rates (IR). Women aged 25–29 years had the highest incidence of cervical precancerous lesions (CIN2: 192.9/10, CIN3: 737.2/10, AIS: 32.5/10(5) in 2016). The IR of CIN2 increased for all screening ages (25–69 years) from 3.6% to 6.7% per year. CIN3 incidence increased by 1.6% (95% confidence interval [CI] 0.6–2.6) annually. A steep increase in AIS incidence was observed in all age groups (7.1% per year, 95% CI 5.3–8.8). Changes in screening tests and the histological verification of cervical precancerous lesions alone cannot explain the steady increase in incidence we observed over the 25‐year study period, and increased exposure to human papillomavirus (HPV) likely plays a role. Age‐appropriate treatment of screening‐detected cervical precancerous lesions is needed for effective cervical cancer control while avoiding overtreatment and related health risks. In order to perform an appropriate harm‐benefit evaluation of cervical cancer control efforts, detailed information on screening technology and background risks, including HPV vaccination status, is needed to create optimal public health policy. John Wiley & Sons, Inc. 2019-03-04 2019-11-15 /pmc/articles/PMC6767573/ /pubmed/30734284 http://dx.doi.org/10.1002/ijc.32195 Text en © 2019 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cancer Epidemiology
Orumaa, Madleen
Leinonen, Maarit K
Campbell, Suzanne
Møller, Bjørn
Myklebust, Tor Åge
Nygård, Mari
Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016
title Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016
title_full Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016
title_fullStr Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016
title_full_unstemmed Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016
title_short Recent increase in incidence of cervical precancerous lesions in Norway: Nationwide study from 1992 to 2016
title_sort recent increase in incidence of cervical precancerous lesions in norway: nationwide study from 1992 to 2016
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767573/
https://www.ncbi.nlm.nih.gov/pubmed/30734284
http://dx.doi.org/10.1002/ijc.32195
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