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Explaining the difference in prognosis between screen-detected and symptomatic breast cancers
BACKGROUND: We analysed 10-year survival data in 19 411 women aged 50–64 years diagnosed with invasive breast cancer in the West Midlands region of the United Kingdom. The aim was to estimate the survival advantage seen in cases that were screen detected compared with those diagnosed symptomatically...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111158/ https://www.ncbi.nlm.nih.gov/pubmed/21540862 http://dx.doi.org/10.1038/bjc.2011.144 |
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author | Allgood, P C Duffy, S W Kearins, O O'Sullivan, E Tappenden, N Wallis, M G Lawrence, G |
author_facet | Allgood, P C Duffy, S W Kearins, O O'Sullivan, E Tappenden, N Wallis, M G Lawrence, G |
author_sort | Allgood, P C |
collection | PubMed |
description | BACKGROUND: We analysed 10-year survival data in 19 411 women aged 50–64 years diagnosed with invasive breast cancer in the West Midlands region of the United Kingdom. The aim was to estimate the survival advantage seen in cases that were screen detected compared with those diagnosed symptomatically and attribute this to shifts in prognostic variables or survival differences specific to prognostic categories. METHODS: We studied tumour size, histological grade and the Nottingham Prognostic Index in very narrow categories and investigated the distribution of these prognostic factors within screen-detected and symptomatic tumours. We also adjusted for lead time bias. RESULTS: The unadjusted 10-year breast cancer survival in screen-detected cases was 85.5% and in symptomatic cases 62.8% after adjustment for lead time bias, survival in the screen-detected cases was 79.3%. Within narrow categories of prognostic variables, survival differences were small, indicating that the majority of the survival advantage of screen detection is due to differences in the distributions of size and node status. CONCLUSION: Our results suggested that a combination of lead time with size and node status in 10 categories explained almost all (97%) of the survival advantage. Only a small proportion remained to be explained by biological differences, manifested as length bias or overdiagnosis. |
format | Online Article Text |
id | pubmed-3111158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31111582012-05-24 Explaining the difference in prognosis between screen-detected and symptomatic breast cancers Allgood, P C Duffy, S W Kearins, O O'Sullivan, E Tappenden, N Wallis, M G Lawrence, G Br J Cancer Clinical Study BACKGROUND: We analysed 10-year survival data in 19 411 women aged 50–64 years diagnosed with invasive breast cancer in the West Midlands region of the United Kingdom. The aim was to estimate the survival advantage seen in cases that were screen detected compared with those diagnosed symptomatically and attribute this to shifts in prognostic variables or survival differences specific to prognostic categories. METHODS: We studied tumour size, histological grade and the Nottingham Prognostic Index in very narrow categories and investigated the distribution of these prognostic factors within screen-detected and symptomatic tumours. We also adjusted for lead time bias. RESULTS: The unadjusted 10-year breast cancer survival in screen-detected cases was 85.5% and in symptomatic cases 62.8% after adjustment for lead time bias, survival in the screen-detected cases was 79.3%. Within narrow categories of prognostic variables, survival differences were small, indicating that the majority of the survival advantage of screen detection is due to differences in the distributions of size and node status. CONCLUSION: Our results suggested that a combination of lead time with size and node status in 10 categories explained almost all (97%) of the survival advantage. Only a small proportion remained to be explained by biological differences, manifested as length bias or overdiagnosis. Nature Publishing Group 2011-05-24 2011-05-03 /pmc/articles/PMC3111158/ /pubmed/21540862 http://dx.doi.org/10.1038/bjc.2011.144 Text en Copyright © 2011 Cancer Research UK 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 | Clinical Study Allgood, P C Duffy, S W Kearins, O O'Sullivan, E Tappenden, N Wallis, M G Lawrence, G Explaining the difference in prognosis between screen-detected and symptomatic breast cancers |
title | Explaining the difference in prognosis between screen-detected and symptomatic breast cancers |
title_full | Explaining the difference in prognosis between screen-detected and symptomatic breast cancers |
title_fullStr | Explaining the difference in prognosis between screen-detected and symptomatic breast cancers |
title_full_unstemmed | Explaining the difference in prognosis between screen-detected and symptomatic breast cancers |
title_short | Explaining the difference in prognosis between screen-detected and symptomatic breast cancers |
title_sort | explaining the difference in prognosis between screen-detected and symptomatic breast cancers |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111158/ https://www.ncbi.nlm.nih.gov/pubmed/21540862 http://dx.doi.org/10.1038/bjc.2011.144 |
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