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A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial
Recent evidence demonstrated CIN4 as a predictive marker of anthracycline benefit in early breast cancer. An analysis of the NCIC CTG MA.21 clinical trial was performed to test the role of existing CIN gene expression signatures as prognostic and predictive markers in the context of taxane based che...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226493/ https://www.ncbi.nlm.nih.gov/pubmed/27056899 http://dx.doi.org/10.18632/oncotarget.8542 |
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author | Spears, Melanie Lyttle, Nicola D'Costa, Alister Chen, Bingshu E. Yao, Cindy Q. Boutros, Paul C. Burnell, Margot Levine, Mark N. O'Brien, Patti Shepherd, Lois Bartlett, John M.S. |
author_facet | Spears, Melanie Lyttle, Nicola D'Costa, Alister Chen, Bingshu E. Yao, Cindy Q. Boutros, Paul C. Burnell, Margot Levine, Mark N. O'Brien, Patti Shepherd, Lois Bartlett, John M.S. |
author_sort | Spears, Melanie |
collection | PubMed |
description | Recent evidence demonstrated CIN4 as a predictive marker of anthracycline benefit in early breast cancer. An analysis of the NCIC CTG MA.21 clinical trial was performed to test the role of existing CIN gene expression signatures as prognostic and predictive markers in the context of taxane based chemotherapy. RNA was extracted from patients in cyclophosphamide, epirubicin and fluorouracil (CEF) and epirubicin, cyclophosphamide and paclitaxel (EC/T) arms of the NCIC CTG MA.21 trial and analysed using NanoString technology. After multivariate analysis both high CIN25 and CIN70 score was significantly associated with an increased in RFS (HR 1.76, 95%CI 1.07-2.86, p=0.0018 and HR 1.59, 95%CI 1.12-2.25, p=0.0096 respectively). Patients whose tumours had low CIN4 gene expression scores were associated with an increase in RFS (HR: 0.64, 95% CI 0.39-1.03, p=0.06) when treated with EC/T compared to patients treated with CEF. In conclusion we have demonstrated CIN25 and CIN70 as prognostic markers in breast cancer and that CIN4 is a potential predictive maker of benefit from taxane treatment. |
format | Online Article Text |
id | pubmed-5226493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52264932017-01-18 A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial Spears, Melanie Lyttle, Nicola D'Costa, Alister Chen, Bingshu E. Yao, Cindy Q. Boutros, Paul C. Burnell, Margot Levine, Mark N. O'Brien, Patti Shepherd, Lois Bartlett, John M.S. Oncotarget Research Paper Recent evidence demonstrated CIN4 as a predictive marker of anthracycline benefit in early breast cancer. An analysis of the NCIC CTG MA.21 clinical trial was performed to test the role of existing CIN gene expression signatures as prognostic and predictive markers in the context of taxane based chemotherapy. RNA was extracted from patients in cyclophosphamide, epirubicin and fluorouracil (CEF) and epirubicin, cyclophosphamide and paclitaxel (EC/T) arms of the NCIC CTG MA.21 trial and analysed using NanoString technology. After multivariate analysis both high CIN25 and CIN70 score was significantly associated with an increased in RFS (HR 1.76, 95%CI 1.07-2.86, p=0.0018 and HR 1.59, 95%CI 1.12-2.25, p=0.0096 respectively). Patients whose tumours had low CIN4 gene expression scores were associated with an increase in RFS (HR: 0.64, 95% CI 0.39-1.03, p=0.06) when treated with EC/T compared to patients treated with CEF. In conclusion we have demonstrated CIN25 and CIN70 as prognostic markers in breast cancer and that CIN4 is a potential predictive maker of benefit from taxane treatment. Impact Journals LLC 2016-04-01 /pmc/articles/PMC5226493/ /pubmed/27056899 http://dx.doi.org/10.18632/oncotarget.8542 Text en Copyright: © 2016 Spears et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Spears, Melanie Lyttle, Nicola D'Costa, Alister Chen, Bingshu E. Yao, Cindy Q. Boutros, Paul C. Burnell, Margot Levine, Mark N. O'Brien, Patti Shepherd, Lois Bartlett, John M.S. A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial |
title | A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial |
title_full | A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial |
title_fullStr | A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial |
title_full_unstemmed | A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial |
title_short | A four gene signature of chromosome instability (CIN4) predicts for benefit from taxanes in the NCIC-CTG MA21 clinical trial |
title_sort | four gene signature of chromosome instability (cin4) predicts for benefit from taxanes in the ncic-ctg ma21 clinical trial |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226493/ https://www.ncbi.nlm.nih.gov/pubmed/27056899 http://dx.doi.org/10.18632/oncotarget.8542 |
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