One Step Nucleic Acid Amplification (OSNA) positive micrometastases and additional histopathological NSLN metastases: Results from a single institution over 53 months
Abstract Introduction The role of sentinel lymph node micrometastases on histopathological analysis is controversial in axillary staging and management in clinically node negative breast cancer. Long-term studies addressing the clinical relevance of occult breast cancer in sentinel lymph nodes based...
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description | Abstract Introduction The role of sentinel lymph node micrometastases on histopathological analysis is controversial in axillary staging and management in clinically node negative breast cancer. Long-term studies addressing the clinical relevance of occult breast cancer in sentinel lymph nodes based on molecular analysis are lacking. One Step Nucleic Acid Amplification (OSNA), a highly sensitive assay of cytokeratin 19 mRNA, is used intra-operatively for the detection of lymph node macro- and micrometastases in breast cancer. Aim The aim of this study is to review the rate of micrometastases and further histopathological NSLN metastases, in our unit following the introduction of OSNA in Guildford. Methods Data was collected prospectively from the period of introduction 01/12/2008 to 31/05/2013. All patients eligible for sentinel lymph node biopsy were offered OSNA and operations were performed by the consultant breast surgeons. Presence or absence of micro-metastases depends on the agreed cut-off point on the amplification curve. On detection of micrometastases (+) and positive but inhibited (i+) metastases, a level 1 axillary clearance (ANC) was performed and for a macrometastasis (++), a level 3 ANC was carried out. Results 66% of the patients had negative SLN ( n = 672) and 34% ( n = 336) had positive sentinel lymph nodes who had further axillary surgery. Of these, 45% ( n = 152/336) had macrometastases, 40% ( n = 136/336) had micrometastases and 15% (48/336) had positive but inhibited results. There was no difference in the patient demographics and tumour characteristics in the various positive SLN groups. In patients with micrometastases, 15% (20/136) had further positive NLSNs and a further 6% (8/136) had >4 overall positive nodes (SLN + NSLN) thus requiring adjuvant supraclavicular/chest wall radiotherapy ( p |
doi_str_mv | 10.1016/j.surge.2014.06.001 |
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Long-term studies addressing the clinical relevance of occult breast cancer in sentinel lymph nodes based on molecular analysis are lacking. One Step Nucleic Acid Amplification (OSNA), a highly sensitive assay of cytokeratin 19 mRNA, is used intra-operatively for the detection of lymph node macro- and micrometastases in breast cancer. Aim The aim of this study is to review the rate of micrometastases and further histopathological NSLN metastases, in our unit following the introduction of OSNA in Guildford. Methods Data was collected prospectively from the period of introduction 01/12/2008 to 31/05/2013. All patients eligible for sentinel lymph node biopsy were offered OSNA and operations were performed by the consultant breast surgeons. Presence or absence of micro-metastases depends on the agreed cut-off point on the amplification curve. On detection of micrometastases (+) and positive but inhibited (i+) metastases, a level 1 axillary clearance (ANC) was performed and for a macrometastasis (++), a level 3 ANC was carried out. Results 66% of the patients had negative SLN ( n = 672) and 34% ( n = 336) had positive sentinel lymph nodes who had further axillary surgery. Of these, 45% ( n = 152/336) had macrometastases, 40% ( n = 136/336) had micrometastases and 15% (48/336) had positive but inhibited results. There was no difference in the patient demographics and tumour characteristics in the various positive SLN groups. In patients with micrometastases, 15% (20/136) had further positive NLSNs and a further 6% (8/136) had >4 overall positive nodes (SLN + NSLN) thus requiring adjuvant supraclavicular/chest wall radiotherapy ( p < 0.05). 25% of node positive patients had further NLSN metastases (85/336) and in these patients, the ratio of positive SLN/harvested SLN (+SLN/SLN) is constant at 1:1. This shows the likelihood of further positive NSLNs if all the harvested lymph nodes are positive. This linear trend is present in both micro-and macrometastases, thus correlating with the size and number of NSLN metastases. Conclusion Our study reflects the tumour burden of NSLNs based on the molecular analysis of the SLN. OSNA has the potential to accurately identify axillary micrometastases. Micro-metastases are important as some of the patients with micrometastases had overall four positive nodes [SLN + NSLN] (criteria for radiotherapy in the absence of other adverse clinicopathological features). Also, our study highlights certain factors that predict the NSLN metastases, pending validation by further prospective long-term data. This will allow accurate calculation of the axillary tumour burden, particularly in patients with micro-metastases.</description><identifier>ISSN: 1479-666X</identifier><identifier>EISSN: 2405-5840</identifier><identifier>DOI: 10.1016/j.surge.2014.06.001</identifier><identifier>PMID: 25444440</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Axilla ; Axillary nodal clearance ; Breast Neoplasms - diagnosis ; Breast Neoplasms - genetics ; Breast Neoplasms - secondary ; DNA, Neoplasm - analysis ; Female ; Follow-Up Studies ; Humans ; Lymph Nodes - pathology ; Micrometastases ; Middle Aged ; Neoplasm Micrometastasis ; Non-sentinel lymph node metastases ; Nucleic Acid Amplification Techniques - methods ; OSNA ; Retrospective Studies ; Sentinel Lymph Node Biopsy - methods ; Surgery ; Time Factors</subject><ispartof>The surgeon (Edinburgh), 2016-04, Vol.14 (2), p.76-81</ispartof><rights>Royal College of Surgeons of Edinburgh (Scottish charity number SC005317) and Royal College of Surgeons in Ireland</rights><rights>2014 Royal College of Surgeons of Edinburgh (Scottish charity number SC005317) and Royal College of Surgeons in Ireland</rights><rights>Copyright © 2014 Royal College of Surgeons of Edinburgh (Scottish charity number SC005317) and Royal College of Surgeons in Ireland. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-c9bd35fc3938e29b22a92c6dc9e7aa6cea9d611e60a068984ac3b9cf736a3a713</citedby><cites>FETCH-LOGICAL-c484t-c9bd35fc3938e29b22a92c6dc9e7aa6cea9d611e60a068984ac3b9cf736a3a713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.surge.2014.06.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25444440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Babar, M</creatorcontrib><creatorcontrib>Madani, R</creatorcontrib><creatorcontrib>Jackson, P</creatorcontrib><creatorcontrib>Layer, G.T</creatorcontrib><creatorcontrib>Kissin, M.W</creatorcontrib><creatorcontrib>Irvine, T.E</creatorcontrib><title>One Step Nucleic Acid Amplification (OSNA) positive micrometastases and additional histopathological NSLN metastases: Results from a single institution over 53 months</title><title>The surgeon (Edinburgh)</title><addtitle>Surgeon</addtitle><description>Abstract Introduction The role of sentinel lymph node micrometastases on histopathological analysis is controversial in axillary staging and management in clinically node negative breast cancer. Long-term studies addressing the clinical relevance of occult breast cancer in sentinel lymph nodes based on molecular analysis are lacking. One Step Nucleic Acid Amplification (OSNA), a highly sensitive assay of cytokeratin 19 mRNA, is used intra-operatively for the detection of lymph node macro- and micrometastases in breast cancer. Aim The aim of this study is to review the rate of micrometastases and further histopathological NSLN metastases, in our unit following the introduction of OSNA in Guildford. Methods Data was collected prospectively from the period of introduction 01/12/2008 to 31/05/2013. All patients eligible for sentinel lymph node biopsy were offered OSNA and operations were performed by the consultant breast surgeons. Presence or absence of micro-metastases depends on the agreed cut-off point on the amplification curve. On detection of micrometastases (+) and positive but inhibited (i+) metastases, a level 1 axillary clearance (ANC) was performed and for a macrometastasis (++), a level 3 ANC was carried out. Results 66% of the patients had negative SLN ( n = 672) and 34% ( n = 336) had positive sentinel lymph nodes who had further axillary surgery. Of these, 45% ( n = 152/336) had macrometastases, 40% ( n = 136/336) had micrometastases and 15% (48/336) had positive but inhibited results. There was no difference in the patient demographics and tumour characteristics in the various positive SLN groups. In patients with micrometastases, 15% (20/136) had further positive NLSNs and a further 6% (8/136) had >4 overall positive nodes (SLN + NSLN) thus requiring adjuvant supraclavicular/chest wall radiotherapy ( p < 0.05). 25% of node positive patients had further NLSN metastases (85/336) and in these patients, the ratio of positive SLN/harvested SLN (+SLN/SLN) is constant at 1:1. This shows the likelihood of further positive NSLNs if all the harvested lymph nodes are positive. This linear trend is present in both micro-and macrometastases, thus correlating with the size and number of NSLN metastases. Conclusion Our study reflects the tumour burden of NSLNs based on the molecular analysis of the SLN. OSNA has the potential to accurately identify axillary micrometastases. Micro-metastases are important as some of the patients with micrometastases had overall four positive nodes [SLN + NSLN] (criteria for radiotherapy in the absence of other adverse clinicopathological features). Also, our study highlights certain factors that predict the NSLN metastases, pending validation by further prospective long-term data. This will allow accurate calculation of the axillary tumour burden, particularly in patients with micro-metastases.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Axilla</subject><subject>Axillary nodal clearance</subject><subject>Breast Neoplasms - diagnosis</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - secondary</subject><subject>DNA, Neoplasm - analysis</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Lymph Nodes - pathology</subject><subject>Micrometastases</subject><subject>Middle Aged</subject><subject>Neoplasm Micrometastasis</subject><subject>Non-sentinel lymph node metastases</subject><subject>Nucleic Acid Amplification Techniques - methods</subject><subject>OSNA</subject><subject>Retrospective Studies</subject><subject>Sentinel Lymph Node Biopsy - methods</subject><subject>Surgery</subject><subject>Time Factors</subject><issn>1479-666X</issn><issn>2405-5840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkt2KEzEUxwdR3Lr6BILkcr1oPZlkMh1BoSx-wdKCVfAupJkzbWpmMs7JFPaFfE4z21XBG0MgN_8PTn4ny55zWHDg6tVxQeOwx0UOXC5ALQD4g2yWSyjmxVLCw2zGZVnNlVLfLrInREeAvBBQPM4u8kJOB2bZz02HbBuxZ-vRenSWrayr2artvWucNdGFjl1ttuvVS9YHctGdkLXODqHFaChdJGa6mpm6dpPYeHZwFENv4iH4sE8Znq23N2v21_CafUYafSTWpBxmGLlu75G5jqKL411nOOHACsHa0MUDPc0eNcYTPrt_L7Ov7999uf44v9l8-HS9uplbuZRxbqtdLYrGikosMa92eW6q3KraVlgaoyyaqlacowIDalktpbFiV9mmFMoIU3JxmV2dc_sh_BiRom4dWfTedBhG0rwshcxlASpJxVma_oJowEb3g2vNcKs56AmQPuo7QHoCpEHpBCi5XtwXjLsW6z-e30SS4M1ZgGnMk8NBk3XYWazdgDbqOrj_FLz9x2-96yYK3_EW6RjGITFKk2jKNejttCPTinAJACUvxS9cXbsf</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Babar, M</creator><creator>Madani, R</creator><creator>Jackson, P</creator><creator>Layer, G.T</creator><creator>Kissin, M.W</creator><creator>Irvine, T.E</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160401</creationdate><title>One Step Nucleic Acid Amplification (OSNA) positive micrometastases and additional histopathological NSLN metastases: Results from a single institution over 53 months</title><author>Babar, M ; Madani, R ; Jackson, P ; Layer, G.T ; Kissin, M.W ; Irvine, T.E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c484t-c9bd35fc3938e29b22a92c6dc9e7aa6cea9d611e60a068984ac3b9cf736a3a713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Axilla</topic><topic>Axillary nodal clearance</topic><topic>Breast Neoplasms - diagnosis</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - secondary</topic><topic>DNA, Neoplasm - analysis</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Lymph Nodes - pathology</topic><topic>Micrometastases</topic><topic>Middle Aged</topic><topic>Neoplasm Micrometastasis</topic><topic>Non-sentinel lymph node metastases</topic><topic>Nucleic Acid Amplification Techniques - methods</topic><topic>OSNA</topic><topic>Retrospective Studies</topic><topic>Sentinel Lymph Node Biopsy - methods</topic><topic>Surgery</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Babar, M</creatorcontrib><creatorcontrib>Madani, R</creatorcontrib><creatorcontrib>Jackson, P</creatorcontrib><creatorcontrib>Layer, G.T</creatorcontrib><creatorcontrib>Kissin, M.W</creatorcontrib><creatorcontrib>Irvine, T.E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The surgeon (Edinburgh)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Babar, M</au><au>Madani, R</au><au>Jackson, P</au><au>Layer, G.T</au><au>Kissin, M.W</au><au>Irvine, T.E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>One Step Nucleic Acid Amplification (OSNA) positive micrometastases and additional histopathological NSLN metastases: Results from a single institution over 53 months</atitle><jtitle>The surgeon (Edinburgh)</jtitle><addtitle>Surgeon</addtitle><date>2016-04-01</date><risdate>2016</risdate><volume>14</volume><issue>2</issue><spage>76</spage><epage>81</epage><pages>76-81</pages><issn>1479-666X</issn><eissn>2405-5840</eissn><abstract>Abstract Introduction The role of sentinel lymph node micrometastases on histopathological analysis is controversial in axillary staging and management in clinically node negative breast cancer. Long-term studies addressing the clinical relevance of occult breast cancer in sentinel lymph nodes based on molecular analysis are lacking. One Step Nucleic Acid Amplification (OSNA), a highly sensitive assay of cytokeratin 19 mRNA, is used intra-operatively for the detection of lymph node macro- and micrometastases in breast cancer. Aim The aim of this study is to review the rate of micrometastases and further histopathological NSLN metastases, in our unit following the introduction of OSNA in Guildford. Methods Data was collected prospectively from the period of introduction 01/12/2008 to 31/05/2013. All patients eligible for sentinel lymph node biopsy were offered OSNA and operations were performed by the consultant breast surgeons. Presence or absence of micro-metastases depends on the agreed cut-off point on the amplification curve. On detection of micrometastases (+) and positive but inhibited (i+) metastases, a level 1 axillary clearance (ANC) was performed and for a macrometastasis (++), a level 3 ANC was carried out. Results 66% of the patients had negative SLN ( n = 672) and 34% ( n = 336) had positive sentinel lymph nodes who had further axillary surgery. Of these, 45% ( n = 152/336) had macrometastases, 40% ( n = 136/336) had micrometastases and 15% (48/336) had positive but inhibited results. There was no difference in the patient demographics and tumour characteristics in the various positive SLN groups. In patients with micrometastases, 15% (20/136) had further positive NLSNs and a further 6% (8/136) had >4 overall positive nodes (SLN + NSLN) thus requiring adjuvant supraclavicular/chest wall radiotherapy ( p < 0.05). 25% of node positive patients had further NLSN metastases (85/336) and in these patients, the ratio of positive SLN/harvested SLN (+SLN/SLN) is constant at 1:1. This shows the likelihood of further positive NSLNs if all the harvested lymph nodes are positive. This linear trend is present in both micro-and macrometastases, thus correlating with the size and number of NSLN metastases. Conclusion Our study reflects the tumour burden of NSLNs based on the molecular analysis of the SLN. OSNA has the potential to accurately identify axillary micrometastases. Micro-metastases are important as some of the patients with micrometastases had overall four positive nodes [SLN + NSLN] (criteria for radiotherapy in the absence of other adverse clinicopathological features). Also, our study highlights certain factors that predict the NSLN metastases, pending validation by further prospective long-term data. This will allow accurate calculation of the axillary tumour burden, particularly in patients with micro-metastases.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>25444440</pmid><doi>10.1016/j.surge.2014.06.001</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Axilla Axillary nodal clearance Breast Neoplasms - diagnosis Breast Neoplasms - genetics Breast Neoplasms - secondary DNA, Neoplasm - analysis Female Follow-Up Studies Humans Lymph Nodes - pathology Micrometastases Middle Aged Neoplasm Micrometastasis Non-sentinel lymph node metastases Nucleic Acid Amplification Techniques - methods OSNA Retrospective Studies Sentinel Lymph Node Biopsy - methods Surgery Time Factors |
title | One Step Nucleic Acid Amplification (OSNA) positive micrometastases and additional histopathological NSLN metastases: Results from a single institution over 53 months |
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