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Axillary staging based on molecular analysis: Results of the B-CLOSER-II study
Axillary staging (pN) is a strong predictor of outcome in early stage breast cancer yet following the publication of the Z0011 trial there has been an increasing tendency to spare lymph node dissection. Automated molecular detection of cytokeratin 19mRNA by one-step nucleic acid amplification (OSNA)...
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Published in: | Pathology, research and practice research and practice, 2020-11, Vol.216 (11), p.153197-153197, Article 153197 |
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creator | Sansano, Irene Vieites, Begoña Sancho de Salas, Magdalena García, Carmen Amendoeira, Isabel Bernet, Laia Pérez-García, José Manuel Espinosa-Bravo, Martín Rubio, Isabel T. Ramón y Cajal, Santiago Peg, Vicente |
description | Axillary staging (pN) is a strong predictor of outcome in early stage breast cancer yet following the publication of the Z0011 trial there has been an increasing tendency to spare lymph node dissection. Automated molecular detection of cytokeratin 19mRNA by one-step nucleic acid amplification (OSNA) has been demonstrated to be an accurate method to assess sentinel lymph node (SLN) metastasis. In this study we compare histological and molecular methods following complete axillary lymph node dissection (cALND), determine whether molecular axillary staging affects survival, and evaluate the predictive and prognostic value of total tumor load in ALND (AD-TTL) and in all positive nodes (G-TTL).
Axillary lymph nodes were collected from 102 patients with primary breast cancer with histological confirmation of axillary involvement (cN+) or positive SLN. The central 1-mm portion of each non-SLN was processed for hematoxylin-eosin staining and the remaining tissue was analyzed by OSNA.
Non-SLNs were diagnosed as positive in 72 out of 102 patients (70.6 %) on OSNA compared with only 53 (52 %) on histology (p < 0.01). Thirteen patients would have changed staging if the diagnoses provided had been by molecular methods (p < 0.01), but without a change in prognosis. AD-TTL and G-TTL were predictive of recurrence and mortality.
Compared to molecular detection, histological examination significantly underestimates the frequency of axillary node metastases. However, the increase in pN did not show a clinical effect on survival in those patients. |
doi_str_mv | 10.1016/j.prp.2020.153197 |
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Axillary lymph nodes were collected from 102 patients with primary breast cancer with histological confirmation of axillary involvement (cN+) or positive SLN. The central 1-mm portion of each non-SLN was processed for hematoxylin-eosin staining and the remaining tissue was analyzed by OSNA.
Non-SLNs were diagnosed as positive in 72 out of 102 patients (70.6 %) on OSNA compared with only 53 (52 %) on histology (p < 0.01). Thirteen patients would have changed staging if the diagnoses provided had been by molecular methods (p < 0.01), but without a change in prognosis. AD-TTL and G-TTL were predictive of recurrence and mortality.
Compared to molecular detection, histological examination significantly underestimates the frequency of axillary node metastases. However, the increase in pN did not show a clinical effect on survival in those patients.</description><identifier>ISSN: 0344-0338</identifier><identifier>EISSN: 1618-0631</identifier><identifier>DOI: 10.1016/j.prp.2020.153197</identifier><language>eng</language><publisher>Elsevier GmbH</publisher><subject>Breast cancer ; Molecular axillary staging ; OSNA ; Prognosis</subject><ispartof>Pathology, research and practice, 2020-11, Vol.216 (11), p.153197-153197, Article 153197</ispartof><rights>2020 Elsevier GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c330t-f266b7774d5c8a40037c2ad1536cb3ad29e6efd8ec69b69a1a8e2c4a77f397c43</citedby><cites>FETCH-LOGICAL-c330t-f266b7774d5c8a40037c2ad1536cb3ad29e6efd8ec69b69a1a8e2c4a77f397c43</cites><orcidid>0000-0003-0188-5210 ; 0000-0002-4293-3875 ; 0000-0003-0035-0679 ; 0000-0003-2611-8501 ; 0000-0002-3867-1390 ; 0000-0002-5203-6166</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Sansano, Irene</creatorcontrib><creatorcontrib>Vieites, Begoña</creatorcontrib><creatorcontrib>Sancho de Salas, Magdalena</creatorcontrib><creatorcontrib>García, Carmen</creatorcontrib><creatorcontrib>Amendoeira, Isabel</creatorcontrib><creatorcontrib>Bernet, Laia</creatorcontrib><creatorcontrib>Pérez-García, José Manuel</creatorcontrib><creatorcontrib>Espinosa-Bravo, Martín</creatorcontrib><creatorcontrib>Rubio, Isabel T.</creatorcontrib><creatorcontrib>Ramón y Cajal, Santiago</creatorcontrib><creatorcontrib>Peg, Vicente</creatorcontrib><title>Axillary staging based on molecular analysis: Results of the B-CLOSER-II study</title><title>Pathology, research and practice</title><description>Axillary staging (pN) is a strong predictor of outcome in early stage breast cancer yet following the publication of the Z0011 trial there has been an increasing tendency to spare lymph node dissection. Automated molecular detection of cytokeratin 19mRNA by one-step nucleic acid amplification (OSNA) has been demonstrated to be an accurate method to assess sentinel lymph node (SLN) metastasis. In this study we compare histological and molecular methods following complete axillary lymph node dissection (cALND), determine whether molecular axillary staging affects survival, and evaluate the predictive and prognostic value of total tumor load in ALND (AD-TTL) and in all positive nodes (G-TTL).
Axillary lymph nodes were collected from 102 patients with primary breast cancer with histological confirmation of axillary involvement (cN+) or positive SLN. The central 1-mm portion of each non-SLN was processed for hematoxylin-eosin staining and the remaining tissue was analyzed by OSNA.
Non-SLNs were diagnosed as positive in 72 out of 102 patients (70.6 %) on OSNA compared with only 53 (52 %) on histology (p < 0.01). Thirteen patients would have changed staging if the diagnoses provided had been by molecular methods (p < 0.01), but without a change in prognosis. AD-TTL and G-TTL were predictive of recurrence and mortality.
Compared to molecular detection, histological examination significantly underestimates the frequency of axillary node metastases. However, the increase in pN did not show a clinical effect on survival in those patients.</description><subject>Breast cancer</subject><subject>Molecular axillary staging</subject><subject>OSNA</subject><subject>Prognosis</subject><issn>0344-0338</issn><issn>1618-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OwzAQhC0EEqXwANx85JLiv9oJnKAqUKmiUoGz5dib4ipNgp0g-va4KmdOq92db7UzCF1TMqGEytvtpAvdhBGW-imnhTpBIyppnhHJ6SkaES5ERjjPz9FFjFtCiCKCjtDrw4-vaxP2OPZm45sNLk0Eh9sG79oa7JB22DSm3kcf7_Aa4lD3EbcV7j8BP2az5eptvs4Wi8QPbn-JzipTR7j6q2P08TR_n71ky9XzYvawzCznpM8qJmWplBJuanMjCOHKMuPS59KW3DhWgITK5WBlUcrCUJMDs8IoVfFCWcHH6OZ4twvt1wCx1zsfLSQnDbRD1EwIxhhPrpOUHqU2tDEGqHQX_C451pToQ3Z6myadPmSnj9kl5v7IQPLw7SHoaD00FpwPYHvtWv8P_QuKeXYU</recordid><startdate>202011</startdate><enddate>202011</enddate><creator>Sansano, Irene</creator><creator>Vieites, Begoña</creator><creator>Sancho de Salas, Magdalena</creator><creator>García, Carmen</creator><creator>Amendoeira, Isabel</creator><creator>Bernet, Laia</creator><creator>Pérez-García, José Manuel</creator><creator>Espinosa-Bravo, Martín</creator><creator>Rubio, Isabel T.</creator><creator>Ramón y Cajal, Santiago</creator><creator>Peg, Vicente</creator><general>Elsevier GmbH</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0188-5210</orcidid><orcidid>https://orcid.org/0000-0002-4293-3875</orcidid><orcidid>https://orcid.org/0000-0003-0035-0679</orcidid><orcidid>https://orcid.org/0000-0003-2611-8501</orcidid><orcidid>https://orcid.org/0000-0002-3867-1390</orcidid><orcidid>https://orcid.org/0000-0002-5203-6166</orcidid></search><sort><creationdate>202011</creationdate><title>Axillary staging based on molecular analysis: Results of the B-CLOSER-II study</title><author>Sansano, Irene ; Vieites, Begoña ; Sancho de Salas, Magdalena ; García, Carmen ; Amendoeira, Isabel ; Bernet, Laia ; Pérez-García, José Manuel ; Espinosa-Bravo, Martín ; Rubio, Isabel T. ; Ramón y Cajal, Santiago ; Peg, Vicente</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c330t-f266b7774d5c8a40037c2ad1536cb3ad29e6efd8ec69b69a1a8e2c4a77f397c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Breast cancer</topic><topic>Molecular axillary staging</topic><topic>OSNA</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sansano, Irene</creatorcontrib><creatorcontrib>Vieites, Begoña</creatorcontrib><creatorcontrib>Sancho de Salas, Magdalena</creatorcontrib><creatorcontrib>García, Carmen</creatorcontrib><creatorcontrib>Amendoeira, Isabel</creatorcontrib><creatorcontrib>Bernet, Laia</creatorcontrib><creatorcontrib>Pérez-García, José Manuel</creatorcontrib><creatorcontrib>Espinosa-Bravo, Martín</creatorcontrib><creatorcontrib>Rubio, Isabel T.</creatorcontrib><creatorcontrib>Ramón y Cajal, Santiago</creatorcontrib><creatorcontrib>Peg, Vicente</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pathology, research and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sansano, Irene</au><au>Vieites, Begoña</au><au>Sancho de Salas, Magdalena</au><au>García, Carmen</au><au>Amendoeira, Isabel</au><au>Bernet, Laia</au><au>Pérez-García, José Manuel</au><au>Espinosa-Bravo, Martín</au><au>Rubio, Isabel T.</au><au>Ramón y Cajal, Santiago</au><au>Peg, Vicente</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Axillary staging based on molecular analysis: Results of the B-CLOSER-II study</atitle><jtitle>Pathology, research and practice</jtitle><date>2020-11</date><risdate>2020</risdate><volume>216</volume><issue>11</issue><spage>153197</spage><epage>153197</epage><pages>153197-153197</pages><artnum>153197</artnum><issn>0344-0338</issn><eissn>1618-0631</eissn><abstract>Axillary staging (pN) is a strong predictor of outcome in early stage breast cancer yet following the publication of the Z0011 trial there has been an increasing tendency to spare lymph node dissection. Automated molecular detection of cytokeratin 19mRNA by one-step nucleic acid amplification (OSNA) has been demonstrated to be an accurate method to assess sentinel lymph node (SLN) metastasis. In this study we compare histological and molecular methods following complete axillary lymph node dissection (cALND), determine whether molecular axillary staging affects survival, and evaluate the predictive and prognostic value of total tumor load in ALND (AD-TTL) and in all positive nodes (G-TTL).
Axillary lymph nodes were collected from 102 patients with primary breast cancer with histological confirmation of axillary involvement (cN+) or positive SLN. The central 1-mm portion of each non-SLN was processed for hematoxylin-eosin staining and the remaining tissue was analyzed by OSNA.
Non-SLNs were diagnosed as positive in 72 out of 102 patients (70.6 %) on OSNA compared with only 53 (52 %) on histology (p < 0.01). Thirteen patients would have changed staging if the diagnoses provided had been by molecular methods (p < 0.01), but without a change in prognosis. AD-TTL and G-TTL were predictive of recurrence and mortality.
Compared to molecular detection, histological examination significantly underestimates the frequency of axillary node metastases. However, the increase in pN did not show a clinical effect on survival in those patients.</abstract><pub>Elsevier GmbH</pub><doi>10.1016/j.prp.2020.153197</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-0188-5210</orcidid><orcidid>https://orcid.org/0000-0002-4293-3875</orcidid><orcidid>https://orcid.org/0000-0003-0035-0679</orcidid><orcidid>https://orcid.org/0000-0003-2611-8501</orcidid><orcidid>https://orcid.org/0000-0002-3867-1390</orcidid><orcidid>https://orcid.org/0000-0002-5203-6166</orcidid></addata></record> |
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subjects | Breast cancer Molecular axillary staging OSNA Prognosis |
title | Axillary staging based on molecular analysis: Results of the B-CLOSER-II study |
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