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A simple way to measure the burden of interval cancers in breast cancer screening
BACKGROUND: The sensitivity of a mammography program is normally evaluated by comparing the interval cancer rate to the expected breast cancer incidence without screening, i.e. the proportional interval cancer rate (PICR). The expected breast cancer incidence in absence of screening is, however, dif...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219107/ https://www.ncbi.nlm.nih.gov/pubmed/25344115 http://dx.doi.org/10.1186/1471-2407-14-782 |
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author | Andersen, Sune Bangsbøll Törnberg, Sven Lynge, Elsebeth Von Euler-Chelpin, My Njor, Sisse Helle |
author_facet | Andersen, Sune Bangsbøll Törnberg, Sven Lynge, Elsebeth Von Euler-Chelpin, My Njor, Sisse Helle |
author_sort | Andersen, Sune Bangsbøll |
collection | PubMed |
description | BACKGROUND: The sensitivity of a mammography program is normally evaluated by comparing the interval cancer rate to the expected breast cancer incidence without screening, i.e. the proportional interval cancer rate (PICR). The expected breast cancer incidence in absence of screening is, however, difficult to estimate when a program has been running for some time. As an alternative to the PICR we propose the interval cancer ratio [Image: see text]. We validated this simple measure by comparing it with the traditionally used PICR. METHOD: We undertook a systematic review and included studies: 1) covering a service screening program, 2) women aged 50-69 years, 3) observed data, 4) interval cancers, women screened, or interval cancer rate, screen detected cases, or screen detection rate, and 5) estimated breast cancer incidence rate of background population. This resulted in 5 papers describing 12 mammography screening programs. RESULTS: Covering initial screens only, the ICR varied from 0.10 to 0.28 while the PICR varied from 0.22 to 0.51. For subsequent screens only, the ICR varied from 0.22 to 0.37 and the PICR from 0.28 to 0.51. There was a strong positive correlation between the ICR and the PICR for initial screens (r = 0.81), but less so for subsequent screens (r = 0.65). CONCLUSION: This alternate measure seems to capture the burden of interval cancers just as well as the traditional PICR, without need for the increasingly difficult estimation of background incidence, making it a more accessible tool when evaluating mammography screening program performance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-782) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4219107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42191072014-11-05 A simple way to measure the burden of interval cancers in breast cancer screening Andersen, Sune Bangsbøll Törnberg, Sven Lynge, Elsebeth Von Euler-Chelpin, My Njor, Sisse Helle BMC Cancer Research Article BACKGROUND: The sensitivity of a mammography program is normally evaluated by comparing the interval cancer rate to the expected breast cancer incidence without screening, i.e. the proportional interval cancer rate (PICR). The expected breast cancer incidence in absence of screening is, however, difficult to estimate when a program has been running for some time. As an alternative to the PICR we propose the interval cancer ratio [Image: see text]. We validated this simple measure by comparing it with the traditionally used PICR. METHOD: We undertook a systematic review and included studies: 1) covering a service screening program, 2) women aged 50-69 years, 3) observed data, 4) interval cancers, women screened, or interval cancer rate, screen detected cases, or screen detection rate, and 5) estimated breast cancer incidence rate of background population. This resulted in 5 papers describing 12 mammography screening programs. RESULTS: Covering initial screens only, the ICR varied from 0.10 to 0.28 while the PICR varied from 0.22 to 0.51. For subsequent screens only, the ICR varied from 0.22 to 0.37 and the PICR from 0.28 to 0.51. There was a strong positive correlation between the ICR and the PICR for initial screens (r = 0.81), but less so for subsequent screens (r = 0.65). CONCLUSION: This alternate measure seems to capture the burden of interval cancers just as well as the traditional PICR, without need for the increasingly difficult estimation of background incidence, making it a more accessible tool when evaluating mammography screening program performance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-782) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-24 /pmc/articles/PMC4219107/ /pubmed/25344115 http://dx.doi.org/10.1186/1471-2407-14-782 Text en © Andersen et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Andersen, Sune Bangsbøll Törnberg, Sven Lynge, Elsebeth Von Euler-Chelpin, My Njor, Sisse Helle A simple way to measure the burden of interval cancers in breast cancer screening |
title | A simple way to measure the burden of interval cancers in breast cancer screening |
title_full | A simple way to measure the burden of interval cancers in breast cancer screening |
title_fullStr | A simple way to measure the burden of interval cancers in breast cancer screening |
title_full_unstemmed | A simple way to measure the burden of interval cancers in breast cancer screening |
title_short | A simple way to measure the burden of interval cancers in breast cancer screening |
title_sort | simple way to measure the burden of interval cancers in breast cancer screening |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219107/ https://www.ncbi.nlm.nih.gov/pubmed/25344115 http://dx.doi.org/10.1186/1471-2407-14-782 |
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