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Cancer morbidity trends and regional differences in England—A Bayesian analysis

Reliable modelling of the dynamics of cancer morbidity risk is important, not least due to its significant impact on healthcare and related policies. We identify morbidity trends and regional differences in England for all-cancer and type-specific incidence between 1981 and 2016. We use Bayesian mod...

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Autores principales: Arık, Ayşe, Dodd, Erengul, Streftaris, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239391/
https://www.ncbi.nlm.nih.gov/pubmed/32433663
http://dx.doi.org/10.1371/journal.pone.0232844
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author Arık, Ayşe
Dodd, Erengul
Streftaris, George
author_facet Arık, Ayşe
Dodd, Erengul
Streftaris, George
author_sort Arık, Ayşe
collection PubMed
description Reliable modelling of the dynamics of cancer morbidity risk is important, not least due to its significant impact on healthcare and related policies. We identify morbidity trends and regional differences in England for all-cancer and type-specific incidence between 1981 and 2016. We use Bayesian modelling to estimate cancer morbidity incidence at various age, year, gender, and region levels. Our analysis shows increasing trends in most rates and marked regional variations that also appear to intensify through time in most cases. All-cancer rates have increased significantly, with the highest increase in East, North West and North East. The absolute difference between the rates in the highest- and lowest-incidence region, per 100,000 people, has widened from 39 (95% CI 33-45) to 86 (78-94) for females, and from 94 (85-104) to 116 (105-127) for males. Lung cancer incidence for females has shown the highest increase in Yorkshire and the Humber, while for males it has declined in all regions with the highest decrease in London. The gap between the highest- and lowest-incidence region for females has widened from 47 (42-51) to 94 (88-100). Temporal change in in bowel cancer risk is less manifested, with regional heterogeneity also declining. Prostate cancer incidence has increased with the highest increase in London, and the regional gap has expanded from 33 (30-36) to 76 (69-83). For breast cancer incidence the highest increase has occurred in North East, while the regional variation shows a less discernible increase. The analysis reveals that there are important regional differences in the incidence of all-type and type-specific cancers, and that most of these regional differences become more pronounced over time. A significant increase in regional variation has been demonstrated for most types of cancer examined here, except for bowel cancer where differences have narrowed.
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spelling pubmed-72393912020-06-03 Cancer morbidity trends and regional differences in England—A Bayesian analysis Arık, Ayşe Dodd, Erengul Streftaris, George PLoS One Research Article Reliable modelling of the dynamics of cancer morbidity risk is important, not least due to its significant impact on healthcare and related policies. We identify morbidity trends and regional differences in England for all-cancer and type-specific incidence between 1981 and 2016. We use Bayesian modelling to estimate cancer morbidity incidence at various age, year, gender, and region levels. Our analysis shows increasing trends in most rates and marked regional variations that also appear to intensify through time in most cases. All-cancer rates have increased significantly, with the highest increase in East, North West and North East. The absolute difference between the rates in the highest- and lowest-incidence region, per 100,000 people, has widened from 39 (95% CI 33-45) to 86 (78-94) for females, and from 94 (85-104) to 116 (105-127) for males. Lung cancer incidence for females has shown the highest increase in Yorkshire and the Humber, while for males it has declined in all regions with the highest decrease in London. The gap between the highest- and lowest-incidence region for females has widened from 47 (42-51) to 94 (88-100). Temporal change in in bowel cancer risk is less manifested, with regional heterogeneity also declining. Prostate cancer incidence has increased with the highest increase in London, and the regional gap has expanded from 33 (30-36) to 76 (69-83). For breast cancer incidence the highest increase has occurred in North East, while the regional variation shows a less discernible increase. The analysis reveals that there are important regional differences in the incidence of all-type and type-specific cancers, and that most of these regional differences become more pronounced over time. A significant increase in regional variation has been demonstrated for most types of cancer examined here, except for bowel cancer where differences have narrowed. Public Library of Science 2020-05-20 /pmc/articles/PMC7239391/ /pubmed/32433663 http://dx.doi.org/10.1371/journal.pone.0232844 Text en © 2020 Arık et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Arık, Ayşe
Dodd, Erengul
Streftaris, George
Cancer morbidity trends and regional differences in England—A Bayesian analysis
title Cancer morbidity trends and regional differences in England—A Bayesian analysis
title_full Cancer morbidity trends and regional differences in England—A Bayesian analysis
title_fullStr Cancer morbidity trends and regional differences in England—A Bayesian analysis
title_full_unstemmed Cancer morbidity trends and regional differences in England—A Bayesian analysis
title_short Cancer morbidity trends and regional differences in England—A Bayesian analysis
title_sort cancer morbidity trends and regional differences in england—a bayesian analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239391/
https://www.ncbi.nlm.nih.gov/pubmed/32433663
http://dx.doi.org/10.1371/journal.pone.0232844
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