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Circulating tumor cells in non-metastatic triple-negative breast cancer
Circulating tumor cells (CTCs) can be identified in approximately 25 % of stage I-III breast cancer patients; CTCs presence is a predictor of poor outcome in metastatic breast cancer, but little is known regarding the prognostic significance of CTCs in non-metastatic triple-negative 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/PMC4149877/ https://www.ncbi.nlm.nih.gov/pubmed/25164970 http://dx.doi.org/10.1007/s10549-014-3103-7 |
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author | Karhade, Mandar Hall, Carolyn Mishra, Priyankana Anderson, Amber Kuerer, Henry Bedrosian, Isabelle Krishnamurthy, Savitri Lucci, Anthony |
author_facet | Karhade, Mandar Hall, Carolyn Mishra, Priyankana Anderson, Amber Kuerer, Henry Bedrosian, Isabelle Krishnamurthy, Savitri Lucci, Anthony |
author_sort | Karhade, Mandar |
collection | PubMed |
description | Circulating tumor cells (CTCs) can be identified in approximately 25 % of stage I-III breast cancer patients; CTCs presence is a predictor of poor outcome in metastatic breast cancer, but little is known regarding the prognostic significance of CTCs in non-metastatic triple-negative breast cancer (TNBC) patients. The aim of this study was to determine whether CTCs predict worse outcome in non-metastatic TNBC patients. We evaluated CTCs in 113 patients with stages I-III TNBC at the time of definitive surgery. CTCs were assessed using the CellSearch System(®). Progression-free and overall survival were defined as time elapsed between date of diagnosis and either date of clinical disease progression, death, or last follow-up. Log-rank test and Cox regression analysis were used to determine associations of CTCs with progression-free and overall survival. The median follow-up was 40 months. CTCs were identified in 23/113 (20 %) of patients. No primary tumor characteristic or lymph node status predicted the presence of CTCs. The identification of ≥2 CTCs predicted shorter progression-free (log rank P ≤ 0.001; hazard ratio 8.30, 95 % CI 2.61–26.37) and overall survival (log rank P = 0.0004; hazard ratio 7.19, 95 % CI 1.98–26.06) versus survival for patients with <2 CTCs. Two or more CTCs predict shorter progression-free and overall survival in TNBC patients. Larger studies are needed to determine whether CTC assessment provides beneficial information that could be used in stratifying TNBC patients at increased risk for disease progression. Finally, CTCs characterization could facilitate the development of novel treatment approaches for TNBC. |
format | Online Article Text |
id | pubmed-4149877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-41498772014-09-02 Circulating tumor cells in non-metastatic triple-negative breast cancer Karhade, Mandar Hall, Carolyn Mishra, Priyankana Anderson, Amber Kuerer, Henry Bedrosian, Isabelle Krishnamurthy, Savitri Lucci, Anthony Breast Cancer Res Treat Preclinical Study Circulating tumor cells (CTCs) can be identified in approximately 25 % of stage I-III breast cancer patients; CTCs presence is a predictor of poor outcome in metastatic breast cancer, but little is known regarding the prognostic significance of CTCs in non-metastatic triple-negative breast cancer (TNBC) patients. The aim of this study was to determine whether CTCs predict worse outcome in non-metastatic TNBC patients. We evaluated CTCs in 113 patients with stages I-III TNBC at the time of definitive surgery. CTCs were assessed using the CellSearch System(®). Progression-free and overall survival were defined as time elapsed between date of diagnosis and either date of clinical disease progression, death, or last follow-up. Log-rank test and Cox regression analysis were used to determine associations of CTCs with progression-free and overall survival. The median follow-up was 40 months. CTCs were identified in 23/113 (20 %) of patients. No primary tumor characteristic or lymph node status predicted the presence of CTCs. The identification of ≥2 CTCs predicted shorter progression-free (log rank P ≤ 0.001; hazard ratio 8.30, 95 % CI 2.61–26.37) and overall survival (log rank P = 0.0004; hazard ratio 7.19, 95 % CI 1.98–26.06) versus survival for patients with <2 CTCs. Two or more CTCs predict shorter progression-free and overall survival in TNBC patients. Larger studies are needed to determine whether CTC assessment provides beneficial information that could be used in stratifying TNBC patients at increased risk for disease progression. Finally, CTCs characterization could facilitate the development of novel treatment approaches for TNBC. Springer US 2014-08-28 2014 /pmc/articles/PMC4149877/ /pubmed/25164970 http://dx.doi.org/10.1007/s10549-014-3103-7 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by-nc/4.0/ 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 | Preclinical Study Karhade, Mandar Hall, Carolyn Mishra, Priyankana Anderson, Amber Kuerer, Henry Bedrosian, Isabelle Krishnamurthy, Savitri Lucci, Anthony Circulating tumor cells in non-metastatic triple-negative breast cancer |
title | Circulating tumor cells in non-metastatic triple-negative breast cancer |
title_full | Circulating tumor cells in non-metastatic triple-negative breast cancer |
title_fullStr | Circulating tumor cells in non-metastatic triple-negative breast cancer |
title_full_unstemmed | Circulating tumor cells in non-metastatic triple-negative breast cancer |
title_short | Circulating tumor cells in non-metastatic triple-negative breast cancer |
title_sort | circulating tumor cells in non-metastatic triple-negative breast cancer |
topic | Preclinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149877/ https://www.ncbi.nlm.nih.gov/pubmed/25164970 http://dx.doi.org/10.1007/s10549-014-3103-7 |
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