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Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data

BACKGROUND: We describe temporal trends in breast cancer incidence by molecular subtypes in Scotland because public health prevention programmes, diagnostic and therapeutic services are shaped by differences in tumour biology. METHODS: Population-based cancer registry data on 72,217 women diagnosed...

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Autores principales: Mesa-Eguiagaray, Ines, Wild, Sarah H., Rosenberg, Philip S., Bird, Sheila M., Brewster, David H., Hall, Peter S., Cameron, David A., Morrison, David, Figueroa, Jonine D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463252/
https://www.ncbi.nlm.nih.gov/pubmed/32555534
http://dx.doi.org/10.1038/s41416-020-0938-z
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author Mesa-Eguiagaray, Ines
Wild, Sarah H.
Rosenberg, Philip S.
Bird, Sheila M.
Brewster, David H.
Hall, Peter S.
Cameron, David A.
Morrison, David
Figueroa, Jonine D.
author_facet Mesa-Eguiagaray, Ines
Wild, Sarah H.
Rosenberg, Philip S.
Bird, Sheila M.
Brewster, David H.
Hall, Peter S.
Cameron, David A.
Morrison, David
Figueroa, Jonine D.
author_sort Mesa-Eguiagaray, Ines
collection PubMed
description BACKGROUND: We describe temporal trends in breast cancer incidence by molecular subtypes in Scotland because public health prevention programmes, diagnostic and therapeutic services are shaped by differences in tumour biology. METHODS: Population-based cancer registry data on 72,217 women diagnosed with incident primary breast cancer from 1997 to 2016 were analysed. Age-standardised rates (ASR) and age-specific incidence were estimated by tumour subtype after imputing the 8% of missing oestrogen receptor (ER) status. Joinpoint regression and age–period–cohort models were used to assess whether significant differences were observed in incidence trends by ER status. RESULTS: Overall, ER-positive tumour incidence increased by 0.4%/year (95% confidence interval (CI): −0.1, 1.0). Among routinely screened women aged 50–69 years, we observed an increase in ASR from 1997 to 2011 (1.6%/year, 95% CI: 1.2–2.1). ER-negative tumour incidence decreased among all ages by 2.5%/year (95% CI: −3.9 to −1.1%) over the study period. Compared with the 1941–1959 birth cohort, women born in 1912–1940 had lower incidence rate ratios (IRR) for ER+ tumours and women born in 1960–1986 had lower IRR for ER− tumours. CONCLUSIONS: Future incidence and survival reporting should be monitored by molecular subtypes to inform clinical planning and cancer control programmes.
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spelling pubmed-74632522020-09-11 Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data Mesa-Eguiagaray, Ines Wild, Sarah H. Rosenberg, Philip S. Bird, Sheila M. Brewster, David H. Hall, Peter S. Cameron, David A. Morrison, David Figueroa, Jonine D. Br J Cancer Article BACKGROUND: We describe temporal trends in breast cancer incidence by molecular subtypes in Scotland because public health prevention programmes, diagnostic and therapeutic services are shaped by differences in tumour biology. METHODS: Population-based cancer registry data on 72,217 women diagnosed with incident primary breast cancer from 1997 to 2016 were analysed. Age-standardised rates (ASR) and age-specific incidence were estimated by tumour subtype after imputing the 8% of missing oestrogen receptor (ER) status. Joinpoint regression and age–period–cohort models were used to assess whether significant differences were observed in incidence trends by ER status. RESULTS: Overall, ER-positive tumour incidence increased by 0.4%/year (95% confidence interval (CI): −0.1, 1.0). Among routinely screened women aged 50–69 years, we observed an increase in ASR from 1997 to 2011 (1.6%/year, 95% CI: 1.2–2.1). ER-negative tumour incidence decreased among all ages by 2.5%/year (95% CI: −3.9 to −1.1%) over the study period. Compared with the 1941–1959 birth cohort, women born in 1912–1940 had lower incidence rate ratios (IRR) for ER+ tumours and women born in 1960–1986 had lower IRR for ER− tumours. CONCLUSIONS: Future incidence and survival reporting should be monitored by molecular subtypes to inform clinical planning and cancer control programmes. Nature Publishing Group UK 2020-06-19 2020-09-01 /pmc/articles/PMC7463252/ /pubmed/32555534 http://dx.doi.org/10.1038/s41416-020-0938-z Text en © The Author(s) 2020 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
Mesa-Eguiagaray, Ines
Wild, Sarah H.
Rosenberg, Philip S.
Bird, Sheila M.
Brewster, David H.
Hall, Peter S.
Cameron, David A.
Morrison, David
Figueroa, Jonine D.
Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data
title Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data
title_full Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data
title_fullStr Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data
title_full_unstemmed Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data
title_short Distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of Scottish cancer registry data
title_sort distinct temporal trends in breast cancer incidence from 1997 to 2016 by molecular subtypes: a population-based study of scottish cancer registry data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463252/
https://www.ncbi.nlm.nih.gov/pubmed/32555534
http://dx.doi.org/10.1038/s41416-020-0938-z
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