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Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone?
This paper examines whether screen-detected breast cancer confers additional prognostic benefit to the patient, over and above that expected by any shift in stage at presentation. In all, 5604 women (aged 50–70 years) diagnosed with invasive breast cancer between 1998 and 2003 were identified by the...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410118/ https://www.ncbi.nlm.nih.gov/pubmed/18506175 http://dx.doi.org/10.1038/sj.bjc.6604368 |
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author | Wishart, G C Greenberg, D C Britton, P D Chou, P Brown, C H Purushotham, A D Duffy, S W |
author_facet | Wishart, G C Greenberg, D C Britton, P D Chou, P Brown, C H Purushotham, A D Duffy, S W |
author_sort | Wishart, G C |
collection | PubMed |
description | This paper examines whether screen-detected breast cancer confers additional prognostic benefit to the patient, over and above that expected by any shift in stage at presentation. In all, 5604 women (aged 50–70 years) diagnosed with invasive breast cancer between 1998 and 2003 were identified by the Eastern Cancer Registration and Information Centre (ECRIC) and mammographic screening status was determined. Using proportional hazards regression, we estimated the effect of screen detection compared with symptomatic diagnosis on 5-year survival unadjusted, then adjusted for age and Nottingham Prognostic Index (NPI). A total of 72% of the survival benefit associated with screen-detected breast cancer can be accounted for by age and shift in NPI. Survival analysis by continuous NPI showed a small but systematic survival benefit for screen-detected cancers at each NPI value. These data show that although most of the screen-detected survival advantage is due to a shift in NPI, the mode of detection does impact on survival in patients with equivalent NPI scores. This residual survival benefit is small but significant, and is likely to be due to differences in tumour biology. Current prognostication tools may, therefore, overestimate the benefit of systemic treatments in screen-detected cancers and lead to overtreatment of these patients. |
format | Text |
id | pubmed-2410118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24101182009-09-10 Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? Wishart, G C Greenberg, D C Britton, P D Chou, P Brown, C H Purushotham, A D Duffy, S W Br J Cancer Clinical Study This paper examines whether screen-detected breast cancer confers additional prognostic benefit to the patient, over and above that expected by any shift in stage at presentation. In all, 5604 women (aged 50–70 years) diagnosed with invasive breast cancer between 1998 and 2003 were identified by the Eastern Cancer Registration and Information Centre (ECRIC) and mammographic screening status was determined. Using proportional hazards regression, we estimated the effect of screen detection compared with symptomatic diagnosis on 5-year survival unadjusted, then adjusted for age and Nottingham Prognostic Index (NPI). A total of 72% of the survival benefit associated with screen-detected breast cancer can be accounted for by age and shift in NPI. Survival analysis by continuous NPI showed a small but systematic survival benefit for screen-detected cancers at each NPI value. These data show that although most of the screen-detected survival advantage is due to a shift in NPI, the mode of detection does impact on survival in patients with equivalent NPI scores. This residual survival benefit is small but significant, and is likely to be due to differences in tumour biology. Current prognostication tools may, therefore, overestimate the benefit of systemic treatments in screen-detected cancers and lead to overtreatment of these patients. Nature Publishing Group 2008-06-03 2008-05-27 /pmc/articles/PMC2410118/ /pubmed/18506175 http://dx.doi.org/10.1038/sj.bjc.6604368 Text en Copyright © 2008 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 Wishart, G C Greenberg, D C Britton, P D Chou, P Brown, C H Purushotham, A D Duffy, S W Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? |
title | Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? |
title_full | Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? |
title_fullStr | Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? |
title_full_unstemmed | Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? |
title_short | Screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? |
title_sort | screen-detected vs symptomatic breast cancer: is improved survival due to stage migration alone? |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410118/ https://www.ncbi.nlm.nih.gov/pubmed/18506175 http://dx.doi.org/10.1038/sj.bjc.6604368 |
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