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Comparative pathology of breast cancer in a randomised trial of screening.
In the Edinburgh Randomised Breast Screening Project (EBSP) to December 1988 there were 500 cancers in the study population invited to screening and 340 cancers identified in the control population. The size and negative lymph node status characteristics of invasive cancers from the two populations...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1991
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977297/ https://www.ncbi.nlm.nih.gov/pubmed/1854609 |
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author | Anderson, T. J. Lamb, J. Donnan, P. Alexander, F. E. Huggins, A. Muir, B. B. Kirkpatrick, A. E. Chetty, U. Hepburn, W. Smith, A. |
author_facet | Anderson, T. J. Lamb, J. Donnan, P. Alexander, F. E. Huggins, A. Muir, B. B. Kirkpatrick, A. E. Chetty, U. Hepburn, W. Smith, A. |
author_sort | Anderson, T. J. |
collection | PubMed |
description | In the Edinburgh Randomised Breast Screening Project (EBSP) to December 1988 there were 500 cancers in the study population invited to screening and 340 cancers identified in the control population. The size and negative lymph node status characteristics of invasive cancers from the two populations were significantly different (P less than 0.05). The cancers detected by screening were predominantly 'early stage', with 16% noninvasive (PTIS) and 42% invasive stage I (pT1 node negative), whereas cancers were frequently 'late stage' (more than pT2) and inoperable in nonattenders (44%) and controls (36%). Grouped according to customary size ranges of invasive cancers, the proportion of cases lymph node positive differed in those screen detected compared with controls, but the benefit in favour of screen detection was not constant. In comparisons of cancers detected at prevalence and incidence screens, as a test of conformity with screening theory, no significant differences were apparent according to size and lymph node status, yet the characteristics of histological type of cancer discriminated significantly (P less than 0.05). When these same histological characteristics were used to compare survival, the capacity to separate invasive cancers into two groups having good and poor survival probabilities was evident, with a significant improvement for the screen detected poor survival group compared with controls (P less than 0.05). |
format | Text |
id | pubmed-1977297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19772972009-09-10 Comparative pathology of breast cancer in a randomised trial of screening. Anderson, T. J. Lamb, J. Donnan, P. Alexander, F. E. Huggins, A. Muir, B. B. Kirkpatrick, A. E. Chetty, U. Hepburn, W. Smith, A. Br J Cancer Research Article In the Edinburgh Randomised Breast Screening Project (EBSP) to December 1988 there were 500 cancers in the study population invited to screening and 340 cancers identified in the control population. The size and negative lymph node status characteristics of invasive cancers from the two populations were significantly different (P less than 0.05). The cancers detected by screening were predominantly 'early stage', with 16% noninvasive (PTIS) and 42% invasive stage I (pT1 node negative), whereas cancers were frequently 'late stage' (more than pT2) and inoperable in nonattenders (44%) and controls (36%). Grouped according to customary size ranges of invasive cancers, the proportion of cases lymph node positive differed in those screen detected compared with controls, but the benefit in favour of screen detection was not constant. In comparisons of cancers detected at prevalence and incidence screens, as a test of conformity with screening theory, no significant differences were apparent according to size and lymph node status, yet the characteristics of histological type of cancer discriminated significantly (P less than 0.05). When these same histological characteristics were used to compare survival, the capacity to separate invasive cancers into two groups having good and poor survival probabilities was evident, with a significant improvement for the screen detected poor survival group compared with controls (P less than 0.05). Nature Publishing Group 1991-07 /pmc/articles/PMC1977297/ /pubmed/1854609 Text en 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 | Research Article Anderson, T. J. Lamb, J. Donnan, P. Alexander, F. E. Huggins, A. Muir, B. B. Kirkpatrick, A. E. Chetty, U. Hepburn, W. Smith, A. Comparative pathology of breast cancer in a randomised trial of screening. |
title | Comparative pathology of breast cancer in a randomised trial of screening. |
title_full | Comparative pathology of breast cancer in a randomised trial of screening. |
title_fullStr | Comparative pathology of breast cancer in a randomised trial of screening. |
title_full_unstemmed | Comparative pathology of breast cancer in a randomised trial of screening. |
title_short | Comparative pathology of breast cancer in a randomised trial of screening. |
title_sort | comparative pathology of breast cancer in a randomised trial of screening. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977297/ https://www.ncbi.nlm.nih.gov/pubmed/1854609 |
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