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A prognostic index for operable, node-negative breast cancer

Clinical data and samples from patients diagnosed, more than 10 years previously, with operable node-negative breast cancer (participants in the Scottish Adjuvant Tamoxifen trial), were revisited. Cases with two distinct categories of outcome were selected; more than 10 years disease-free survival (...

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Autores principales: McCallum, M, Baker, C, Gillespie, K, Cohen, B, Stewart, H, Leonard, R, Cameron, D, Leake, R, Paxton, J, Robertson, A, Purdie, C, Gould, A, Steel, M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409476/
https://www.ncbi.nlm.nih.gov/pubmed/15138474
http://dx.doi.org/10.1038/sj.bjc.6601826
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author McCallum, M
Baker, C
Gillespie, K
Cohen, B
Stewart, H
Leonard, R
Cameron, D
Leake, R
Paxton, J
Robertson, A
Purdie, C
Gould, A
Steel, M
author_facet McCallum, M
Baker, C
Gillespie, K
Cohen, B
Stewart, H
Leonard, R
Cameron, D
Leake, R
Paxton, J
Robertson, A
Purdie, C
Gould, A
Steel, M
author_sort McCallum, M
collection PubMed
description Clinical data and samples from patients diagnosed, more than 10 years previously, with operable node-negative breast cancer (participants in the Scottish Adjuvant Tamoxifen trial), were revisited. Cases with two distinct categories of outcome were selected; more than 10 years disease-free survival (‘good outcome’) or distant relapse within 6 years of diagnosis (‘poor outcome’). An initial set of cases was analysed for a range of putative prognostic markers and a prognostic index, distinguishing the two outcome categories, was calculated. This index was then validated by testing its predictive power on a second, independent set of cases. A combination of histological grade plus immunochemical staining for BCL-2, p27 and Cyclin D1, generated a useful prognostic index for tamoxifen-treated patients but not for those treated by surgery alone. The value of the index was confirmed in a second set of tamoxifen-treated, early stage breast cancers. Overall, it correctly predicted good and poor outcome in 79 and 74% of cases, respectively (odds ratio 11.0). Other markers assessed added little to prediction of outcome. In the case of molecular assays, sensitivity and reliability were compromised by the age of the tissue specimens and the variability of fixation protocols. In selecting patients for adjuvant systemic chemotherapy, the proposed index improves considerably on current international guidelines and matches the performance reported for ‘gene-expression signature’ analysis.
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spelling pubmed-24094762009-09-10 A prognostic index for operable, node-negative breast cancer McCallum, M Baker, C Gillespie, K Cohen, B Stewart, H Leonard, R Cameron, D Leake, R Paxton, J Robertson, A Purdie, C Gould, A Steel, M Br J Cancer Molecular and Cellular Pathology Clinical data and samples from patients diagnosed, more than 10 years previously, with operable node-negative breast cancer (participants in the Scottish Adjuvant Tamoxifen trial), were revisited. Cases with two distinct categories of outcome were selected; more than 10 years disease-free survival (‘good outcome’) or distant relapse within 6 years of diagnosis (‘poor outcome’). An initial set of cases was analysed for a range of putative prognostic markers and a prognostic index, distinguishing the two outcome categories, was calculated. This index was then validated by testing its predictive power on a second, independent set of cases. A combination of histological grade plus immunochemical staining for BCL-2, p27 and Cyclin D1, generated a useful prognostic index for tamoxifen-treated patients but not for those treated by surgery alone. The value of the index was confirmed in a second set of tamoxifen-treated, early stage breast cancers. Overall, it correctly predicted good and poor outcome in 79 and 74% of cases, respectively (odds ratio 11.0). Other markers assessed added little to prediction of outcome. In the case of molecular assays, sensitivity and reliability were compromised by the age of the tissue specimens and the variability of fixation protocols. In selecting patients for adjuvant systemic chemotherapy, the proposed index improves considerably on current international guidelines and matches the performance reported for ‘gene-expression signature’ analysis. Nature Publishing Group 2004-05-17 2004-04-27 /pmc/articles/PMC2409476/ /pubmed/15138474 http://dx.doi.org/10.1038/sj.bjc.6601826 Text en Copyright © 2004 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 Molecular and Cellular Pathology
McCallum, M
Baker, C
Gillespie, K
Cohen, B
Stewart, H
Leonard, R
Cameron, D
Leake, R
Paxton, J
Robertson, A
Purdie, C
Gould, A
Steel, M
A prognostic index for operable, node-negative breast cancer
title A prognostic index for operable, node-negative breast cancer
title_full A prognostic index for operable, node-negative breast cancer
title_fullStr A prognostic index for operable, node-negative breast cancer
title_full_unstemmed A prognostic index for operable, node-negative breast cancer
title_short A prognostic index for operable, node-negative breast cancer
title_sort prognostic index for operable, node-negative breast cancer
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409476/
https://www.ncbi.nlm.nih.gov/pubmed/15138474
http://dx.doi.org/10.1038/sj.bjc.6601826
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