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An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients
The one-step nucleic acid amplification (OSNA) assay is a molecular procedure that can identify deposits of breast cancer (BC) cells in the sentinel lymph node (SLN). We examined the consistency of the OSNA assay with a classic hematoxylin-eosin (H&E)-based immunohistochemistry (IHC) study and e...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102897/ https://www.ncbi.nlm.nih.gov/pubmed/25034150 http://dx.doi.org/10.1038/srep05743 |
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author | Ruano, Miguel Alonso Lopez-Bonet, Eugeni Buxó, Maria Tuca-Rodríguez, Francesc Vila-Camps, Ester Alvarez, Elena Martin-Castillo, Begoña Menendez, Javier A. |
author_facet | Ruano, Miguel Alonso Lopez-Bonet, Eugeni Buxó, Maria Tuca-Rodríguez, Francesc Vila-Camps, Ester Alvarez, Elena Martin-Castillo, Begoña Menendez, Javier A. |
author_sort | Ruano, Miguel Alonso |
collection | PubMed |
description | The one-step nucleic acid amplification (OSNA) assay is a molecular procedure that can identify deposits of breast cancer (BC) cells in the sentinel lymph node (SLN). We examined the consistency of the OSNA assay with a classic hematoxylin-eosin (H&E)-based immunohistochemistry (IHC) study and evaluated how OSNA-based axillary staging might impact the therapeutic management of BC patients. SLN biopsy results were considered to be positive in 60 patients (40%) in the OSNA group (N = 148) and in 43 (28%) patients in the IHC cohort (N = 153, p = 0.023). There was no difference in the macrometastasis (22% for OSNA, 15% for H&E, p = 0.139) or micrometastasis (19% for OSNA, 13% for H&E, p = 0.166) rates, but we found statistically significant differences in the number of isolated tumor cells (1% for OSNA, 11% for H&E, p < 0.001). There were no differences in the administration rate of adjuvant systemic therapy between the OSNA (66% in the SLN(+) patients) and the H&E (74% in the SLN(+) patients) groups (p = 0.159). The OSNA assay allows for the detection of SLN metastases more precisely than conventional pathologic methods but does not alter the therapeutic management of SLN(+) BC patients. |
format | Online Article Text |
id | pubmed-4102897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41028972014-07-21 An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients Ruano, Miguel Alonso Lopez-Bonet, Eugeni Buxó, Maria Tuca-Rodríguez, Francesc Vila-Camps, Ester Alvarez, Elena Martin-Castillo, Begoña Menendez, Javier A. Sci Rep Article The one-step nucleic acid amplification (OSNA) assay is a molecular procedure that can identify deposits of breast cancer (BC) cells in the sentinel lymph node (SLN). We examined the consistency of the OSNA assay with a classic hematoxylin-eosin (H&E)-based immunohistochemistry (IHC) study and evaluated how OSNA-based axillary staging might impact the therapeutic management of BC patients. SLN biopsy results were considered to be positive in 60 patients (40%) in the OSNA group (N = 148) and in 43 (28%) patients in the IHC cohort (N = 153, p = 0.023). There was no difference in the macrometastasis (22% for OSNA, 15% for H&E, p = 0.139) or micrometastasis (19% for OSNA, 13% for H&E, p = 0.166) rates, but we found statistically significant differences in the number of isolated tumor cells (1% for OSNA, 11% for H&E, p < 0.001). There were no differences in the administration rate of adjuvant systemic therapy between the OSNA (66% in the SLN(+) patients) and the H&E (74% in the SLN(+) patients) groups (p = 0.159). The OSNA assay allows for the detection of SLN metastases more precisely than conventional pathologic methods but does not alter the therapeutic management of SLN(+) BC patients. Nature Publishing Group 2014-07-18 /pmc/articles/PMC4102897/ /pubmed/25034150 http://dx.doi.org/10.1038/srep05743 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Ruano, Miguel Alonso Lopez-Bonet, Eugeni Buxó, Maria Tuca-Rodríguez, Francesc Vila-Camps, Ester Alvarez, Elena Martin-Castillo, Begoña Menendez, Javier A. An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients |
title | An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients |
title_full | An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients |
title_fullStr | An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients |
title_full_unstemmed | An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients |
title_short | An improved axillary staging system using the OSNA assay does not modify the therapeutic management of breast cancer patients |
title_sort | improved axillary staging system using the osna assay does not modify the therapeutic management of breast cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102897/ https://www.ncbi.nlm.nih.gov/pubmed/25034150 http://dx.doi.org/10.1038/srep05743 |
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