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Predicting a local recurrence after breast-conserving therapy by gene expression profiling
INTRODUCTION: To tailor local treatment in breast cancer patients there is a need for predicting ipsilateral recurrences after breast-conserving therapy. After adequate treatment (excision with free margins and radiotherapy), young age and incompletely excised extensive intraductal component are pre...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779489/ https://www.ncbi.nlm.nih.gov/pubmed/17069664 http://dx.doi.org/10.1186/bcr1614 |
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author | Nuyten, Dimitry SA Kreike, Bas Hart, Augustinus AM Chi, Jen-Tsan Ashley Sneddon, Julie B Wessels, Lodewyk FA Peterse, Hans J Bartelink, Harry Brown, Patrick O Chang, Howard Y van de Vijver, Marc J |
author_facet | Nuyten, Dimitry SA Kreike, Bas Hart, Augustinus AM Chi, Jen-Tsan Ashley Sneddon, Julie B Wessels, Lodewyk FA Peterse, Hans J Bartelink, Harry Brown, Patrick O Chang, Howard Y van de Vijver, Marc J |
author_sort | Nuyten, Dimitry SA |
collection | PubMed |
description | INTRODUCTION: To tailor local treatment in breast cancer patients there is a need for predicting ipsilateral recurrences after breast-conserving therapy. After adequate treatment (excision with free margins and radiotherapy), young age and incompletely excised extensive intraductal component are predictors for local recurrence, but many local recurrences can still not be predicted. Here we have used gene expression profiling by microarray analysis to identify gene expression profiles that can help to predict local recurrence in individual patients. METHODS: By using previously established gene expression profiles with proven value in predicting metastasis-free and overall survival (wound-response signature, 70-gene prognosis profile and hypoxia-induced profile) and training towards an optimal prediction of local recurrences in a training series, we establish a classifier for local recurrence after breast-conserving therapy. RESULTS: Validation of the different gene lists shows that the wound-response signature is able to separate patients with a high (29%) or low (5%) risk of a local recurrence at 10 years (sensitivity 87.5%, specificity 75%). In multivariable analysis the classifier is an independent predictor for local recurrence. CONCLUSION: Our findings indicate that gene expression profiling can identify subgroups of patients at increased risk of developing a local recurrence after breast-conserving therapy. |
format | Text |
id | pubmed-1779489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-17794892007-01-19 Predicting a local recurrence after breast-conserving therapy by gene expression profiling Nuyten, Dimitry SA Kreike, Bas Hart, Augustinus AM Chi, Jen-Tsan Ashley Sneddon, Julie B Wessels, Lodewyk FA Peterse, Hans J Bartelink, Harry Brown, Patrick O Chang, Howard Y van de Vijver, Marc J Breast Cancer Res Research Article INTRODUCTION: To tailor local treatment in breast cancer patients there is a need for predicting ipsilateral recurrences after breast-conserving therapy. After adequate treatment (excision with free margins and radiotherapy), young age and incompletely excised extensive intraductal component are predictors for local recurrence, but many local recurrences can still not be predicted. Here we have used gene expression profiling by microarray analysis to identify gene expression profiles that can help to predict local recurrence in individual patients. METHODS: By using previously established gene expression profiles with proven value in predicting metastasis-free and overall survival (wound-response signature, 70-gene prognosis profile and hypoxia-induced profile) and training towards an optimal prediction of local recurrences in a training series, we establish a classifier for local recurrence after breast-conserving therapy. RESULTS: Validation of the different gene lists shows that the wound-response signature is able to separate patients with a high (29%) or low (5%) risk of a local recurrence at 10 years (sensitivity 87.5%, specificity 75%). In multivariable analysis the classifier is an independent predictor for local recurrence. CONCLUSION: Our findings indicate that gene expression profiling can identify subgroups of patients at increased risk of developing a local recurrence after breast-conserving therapy. BioMed Central 2006 2006-10-30 /pmc/articles/PMC1779489/ /pubmed/17069664 http://dx.doi.org/10.1186/bcr1614 Text en Copyright © 2006 Nuyten et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Nuyten, Dimitry SA Kreike, Bas Hart, Augustinus AM Chi, Jen-Tsan Ashley Sneddon, Julie B Wessels, Lodewyk FA Peterse, Hans J Bartelink, Harry Brown, Patrick O Chang, Howard Y van de Vijver, Marc J Predicting a local recurrence after breast-conserving therapy by gene expression profiling |
title | Predicting a local recurrence after breast-conserving therapy by gene expression profiling |
title_full | Predicting a local recurrence after breast-conserving therapy by gene expression profiling |
title_fullStr | Predicting a local recurrence after breast-conserving therapy by gene expression profiling |
title_full_unstemmed | Predicting a local recurrence after breast-conserving therapy by gene expression profiling |
title_short | Predicting a local recurrence after breast-conserving therapy by gene expression profiling |
title_sort | predicting a local recurrence after breast-conserving therapy by gene expression profiling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779489/ https://www.ncbi.nlm.nih.gov/pubmed/17069664 http://dx.doi.org/10.1186/bcr1614 |
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