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Long-term impact of the 70-gene signature on breast cancer outcome
Several studies have validated the prognostic value of the 70-gene prognosis signature (MammaPrint(R)), but long-term outcome prediction of these patients has not been previously reported. The follow-up of the consecutively treated cohort of 295 patients (<53 years) with invasive breast cancer (T...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907672/ https://www.ncbi.nlm.nih.gov/pubmed/24445566 http://dx.doi.org/10.1007/s10549-013-2831-4 |
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author | Drukker, C. A. van Tinteren, H. Schmidt, M. K. Rutgers, E. J. Th. Bernards, R. van de Vijver, M. J. van’t Veer, L. J. |
author_facet | Drukker, C. A. van Tinteren, H. Schmidt, M. K. Rutgers, E. J. Th. Bernards, R. van de Vijver, M. J. van’t Veer, L. J. |
author_sort | Drukker, C. A. |
collection | PubMed |
description | Several studies have validated the prognostic value of the 70-gene prognosis signature (MammaPrint(R)), but long-term outcome prediction of these patients has not been previously reported. The follow-up of the consecutively treated cohort of 295 patients (<53 years) with invasive breast cancer (T1-2N0-1M0; n = 151 N0, n = 144 N1) diagnosed between 1984 and 1995, in which the 70-gene signature was previously validated, was updated. The median follow-up for this series is now extended to 18.5 years. A significant difference is seen in long-term distant metastasis-free survival (DMFS) for the patients with a low- and a high-risk 70-gene signature (DMFS p < 0.0001), as well as separately for node-negative (DMFS p < 0.0001) and node-positive patients (DMFS p = 0.0004). The 25-year hazard ratios (HRs) for all patients for DMFS and OS were 3.1 (95 % CI 2.02–4.86) and 2.9 (95 % CI 1.90–4.28), respectively. The HRs for DMFS and OS were largest in the first 5 years after diagnosis: 9.6 (95 % CI 4.2–22.1) and 11.3 (95 % CI 3.5–36.4), respectively. The 25-year HRs in the subgroup of node-negative patients for DMFS and OS were 4.57 (95 % CI 2.31–9.04) and 4.73 (95 % CI 2.46–9.07), respectively, and for node-positive patients for DMFS and OS were 2.24 (95 % CI 1.25–4.00) and 1.83 (95 % CI 1.07–3.11), respectively. The 70-gene signature remains prognostic at longer follow-up in patients <53 years of age with stage I and II breast cancer. The 70-gene signature’s strongest prognostic power is seen in the first 5 years after diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10549-013-2831-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3907672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-39076722014-02-04 Long-term impact of the 70-gene signature on breast cancer outcome Drukker, C. A. van Tinteren, H. Schmidt, M. K. Rutgers, E. J. Th. Bernards, R. van de Vijver, M. J. van’t Veer, L. J. Breast Cancer Res Treat Brief Report Several studies have validated the prognostic value of the 70-gene prognosis signature (MammaPrint(R)), but long-term outcome prediction of these patients has not been previously reported. The follow-up of the consecutively treated cohort of 295 patients (<53 years) with invasive breast cancer (T1-2N0-1M0; n = 151 N0, n = 144 N1) diagnosed between 1984 and 1995, in which the 70-gene signature was previously validated, was updated. The median follow-up for this series is now extended to 18.5 years. A significant difference is seen in long-term distant metastasis-free survival (DMFS) for the patients with a low- and a high-risk 70-gene signature (DMFS p < 0.0001), as well as separately for node-negative (DMFS p < 0.0001) and node-positive patients (DMFS p = 0.0004). The 25-year hazard ratios (HRs) for all patients for DMFS and OS were 3.1 (95 % CI 2.02–4.86) and 2.9 (95 % CI 1.90–4.28), respectively. The HRs for DMFS and OS were largest in the first 5 years after diagnosis: 9.6 (95 % CI 4.2–22.1) and 11.3 (95 % CI 3.5–36.4), respectively. The 25-year HRs in the subgroup of node-negative patients for DMFS and OS were 4.57 (95 % CI 2.31–9.04) and 4.73 (95 % CI 2.46–9.07), respectively, and for node-positive patients for DMFS and OS were 2.24 (95 % CI 1.25–4.00) and 1.83 (95 % CI 1.07–3.11), respectively. The 70-gene signature remains prognostic at longer follow-up in patients <53 years of age with stage I and II breast cancer. The 70-gene signature’s strongest prognostic power is seen in the first 5 years after diagnosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10549-013-2831-4) contains supplementary material, which is available to authorized users. Springer US 2014-01-21 2014 /pmc/articles/PMC3907672/ /pubmed/24445566 http://dx.doi.org/10.1007/s10549-013-2831-4 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by-nc/2.5/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Brief Report Drukker, C. A. van Tinteren, H. Schmidt, M. K. Rutgers, E. J. Th. Bernards, R. van de Vijver, M. J. van’t Veer, L. J. Long-term impact of the 70-gene signature on breast cancer outcome |
title | Long-term impact of the 70-gene signature on breast cancer outcome |
title_full | Long-term impact of the 70-gene signature on breast cancer outcome |
title_fullStr | Long-term impact of the 70-gene signature on breast cancer outcome |
title_full_unstemmed | Long-term impact of the 70-gene signature on breast cancer outcome |
title_short | Long-term impact of the 70-gene signature on breast cancer outcome |
title_sort | long-term impact of the 70-gene signature on breast cancer outcome |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907672/ https://www.ncbi.nlm.nih.gov/pubmed/24445566 http://dx.doi.org/10.1007/s10549-013-2831-4 |
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