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Predicting aggressive outcome in T1N0M0 breast cancer

Despite the excellent overall prognosis, unpredictable breast cancer recurrences and deaths also occur among T1N0M0 patients. We have evaluated clinically applicable methods for identifying aggressive outcome in T1N0M0 breast cancer. The material is based on aggressive T1N0M0 invasive ductal and lob...

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Autores principales: Kronqvist, P, Kuopio, T, Nykänen, M, Helenius, H, Anttinen, J, Klemi, P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409808/
https://www.ncbi.nlm.nih.gov/pubmed/15199391
http://dx.doi.org/10.1038/sj.bjc.6601948
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author Kronqvist, P
Kuopio, T
Nykänen, M
Helenius, H
Anttinen, J
Klemi, P
author_facet Kronqvist, P
Kuopio, T
Nykänen, M
Helenius, H
Anttinen, J
Klemi, P
author_sort Kronqvist, P
collection PubMed
description Despite the excellent overall prognosis, unpredictable breast cancer recurrences and deaths also occur among T1N0M0 patients. We have evaluated clinically applicable methods for identifying aggressive outcome in T1N0M0 breast cancer. The material is based on aggressive T1N0M0 invasive ductal and lobular carcinomas diagnosed in Turku University Hospital and Jyväskylä Central Hospital, Finland, during 1987–1997. We studied all the T1N0M0 breast cancers that had led to recurrency or death (n=21, 95% T1cN0M0) during the follow-up period (4–14 years). The study is based on statistical analyses of matched case–control data in which the prognostic factors of each individual patient with aggressive disease were compared with control patients (n=45) individually matched by tumour size, age at diagnosis, histological type of tumour and length of follow-up. The cancer cases were examined for clinically applicable conventional and immunohistochemical pathologic prognostic factors. High Ki-67 immunopositivity was the strongest prognosticator of breast cancer death or recurrence in T1N0M0 breast cancer. Also, high p53 immunopositivity, low oestrogen receptor immunopositivity and Her-2/neu oncogene amplification by chromogen in situ hybridisation were reliable indicators of unfavourable outcome. Our statistical methods also allowed us to determine for the present material a range of clinical significance for each immunohistochemical prognostic feature with the associated relative risk for breast cancer death and recurrence. The paper suggests guidelines for predicting aggressive outcome in T1N0M0 breast cancer.
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spelling pubmed-24098082009-09-10 Predicting aggressive outcome in T1N0M0 breast cancer Kronqvist, P Kuopio, T Nykänen, M Helenius, H Anttinen, J Klemi, P Br J Cancer Molecular and Cellular Pathology Despite the excellent overall prognosis, unpredictable breast cancer recurrences and deaths also occur among T1N0M0 patients. We have evaluated clinically applicable methods for identifying aggressive outcome in T1N0M0 breast cancer. The material is based on aggressive T1N0M0 invasive ductal and lobular carcinomas diagnosed in Turku University Hospital and Jyväskylä Central Hospital, Finland, during 1987–1997. We studied all the T1N0M0 breast cancers that had led to recurrency or death (n=21, 95% T1cN0M0) during the follow-up period (4–14 years). The study is based on statistical analyses of matched case–control data in which the prognostic factors of each individual patient with aggressive disease were compared with control patients (n=45) individually matched by tumour size, age at diagnosis, histological type of tumour and length of follow-up. The cancer cases were examined for clinically applicable conventional and immunohistochemical pathologic prognostic factors. High Ki-67 immunopositivity was the strongest prognosticator of breast cancer death or recurrence in T1N0M0 breast cancer. Also, high p53 immunopositivity, low oestrogen receptor immunopositivity and Her-2/neu oncogene amplification by chromogen in situ hybridisation were reliable indicators of unfavourable outcome. Our statistical methods also allowed us to determine for the present material a range of clinical significance for each immunohistochemical prognostic feature with the associated relative risk for breast cancer death and recurrence. The paper suggests guidelines for predicting aggressive outcome in T1N0M0 breast cancer. Nature Publishing Group 2004-07-19 2004-06-15 /pmc/articles/PMC2409808/ /pubmed/15199391 http://dx.doi.org/10.1038/sj.bjc.6601948 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
Kronqvist, P
Kuopio, T
Nykänen, M
Helenius, H
Anttinen, J
Klemi, P
Predicting aggressive outcome in T1N0M0 breast cancer
title Predicting aggressive outcome in T1N0M0 breast cancer
title_full Predicting aggressive outcome in T1N0M0 breast cancer
title_fullStr Predicting aggressive outcome in T1N0M0 breast cancer
title_full_unstemmed Predicting aggressive outcome in T1N0M0 breast cancer
title_short Predicting aggressive outcome in T1N0M0 breast cancer
title_sort predicting aggressive outcome in t1n0m0 breast cancer
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409808/
https://www.ncbi.nlm.nih.gov/pubmed/15199391
http://dx.doi.org/10.1038/sj.bjc.6601948
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