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Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method

BACKGROUND: The one-step nucleic acid amplification (OSNA) assay is a molecular-based lymph-node metastasis detection procedure that can assess a whole node and yields semi-quantitative results for the detection of clinically relevant nodal metastases. We aimed to determine the performance of the OS...

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Autores principales: Osako, T, Iwase, T, Kimura, K, Yamashita, K, Horii, R, Akiyama, F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3208491/
https://www.ncbi.nlm.nih.gov/pubmed/21878934
http://dx.doi.org/10.1038/bjc.2011.350
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author Osako, T
Iwase, T
Kimura, K
Yamashita, K
Horii, R
Akiyama, F
author_facet Osako, T
Iwase, T
Kimura, K
Yamashita, K
Horii, R
Akiyama, F
author_sort Osako, T
collection PubMed
description BACKGROUND: The one-step nucleic acid amplification (OSNA) assay is a molecular-based lymph-node metastasis detection procedure that can assess a whole node and yields semi-quantitative results for the detection of clinically relevant nodal metastases. We aimed to determine the performance of the OSNA assay as an accurate nodal staging tool in comparison with routine histological examination. METHODS: Subjects comprised 183 consecutive patients with pT1-2 breast cancer who underwent axillary dissection after positive sentinel-node (SN) biopsy with the OSNA assay. Of these, for non-SN evaluation, 119 patients underwent OSNA assay evaluation, whereas 64 had single-section histology. We compared the detection rates of non-SN metastasis and upstaging rates from the SN stage according to the American Joint Committee on Cancer staging between the OSNA and histology cohorts. RESULTS: OSNA detected more cases of non-SN metastases than histology (OSNA 66/119, 55.5% vs histology 13/64, 20.3% P<0.001), particularly micrometastases (36/119, 30.3% vs 1/64, 1.6% P<0.001). Total upstaging rates were similar in both cohorts (20/119, 16.8% vs 9/64, 14.1%, P=0.79). CONCLUSION: OSNA detects a far greater proportion of non-SN micrometastases than routine histological examination. However, upstaging rates after axillary dissection were not significantly different between both cohorts. Follow-up of the OSNA cohort is required to determine its clinical relevance.
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spelling pubmed-32084912012-10-11 Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method Osako, T Iwase, T Kimura, K Yamashita, K Horii, R Akiyama, F Br J Cancer Molecular Diagnostics BACKGROUND: The one-step nucleic acid amplification (OSNA) assay is a molecular-based lymph-node metastasis detection procedure that can assess a whole node and yields semi-quantitative results for the detection of clinically relevant nodal metastases. We aimed to determine the performance of the OSNA assay as an accurate nodal staging tool in comparison with routine histological examination. METHODS: Subjects comprised 183 consecutive patients with pT1-2 breast cancer who underwent axillary dissection after positive sentinel-node (SN) biopsy with the OSNA assay. Of these, for non-SN evaluation, 119 patients underwent OSNA assay evaluation, whereas 64 had single-section histology. We compared the detection rates of non-SN metastasis and upstaging rates from the SN stage according to the American Joint Committee on Cancer staging between the OSNA and histology cohorts. RESULTS: OSNA detected more cases of non-SN metastases than histology (OSNA 66/119, 55.5% vs histology 13/64, 20.3% P<0.001), particularly micrometastases (36/119, 30.3% vs 1/64, 1.6% P<0.001). Total upstaging rates were similar in both cohorts (20/119, 16.8% vs 9/64, 14.1%, P=0.79). CONCLUSION: OSNA detects a far greater proportion of non-SN micrometastases than routine histological examination. However, upstaging rates after axillary dissection were not significantly different between both cohorts. Follow-up of the OSNA cohort is required to determine its clinical relevance. Nature Publishing Group 2011-10-11 2011-08-30 /pmc/articles/PMC3208491/ /pubmed/21878934 http://dx.doi.org/10.1038/bjc.2011.350 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Osako, T
Iwase, T
Kimura, K
Yamashita, K
Horii, R
Akiyama, F
Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method
title Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method
title_full Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method
title_fullStr Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method
title_full_unstemmed Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method
title_short Accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method
title_sort accurate staging of axillary lymph nodes from breast cancer patients using a novel molecular method
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3208491/
https://www.ncbi.nlm.nih.gov/pubmed/21878934
http://dx.doi.org/10.1038/bjc.2011.350
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