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Swedish prospective multicenter trial evaluating sentinel lymph node biopsy after neoadjuvant systemic therapy in clinically node-positive breast cancer
Purpose Patients with clinically node-positive breast cancer planned for neoadjuvant systemic therapy (NAST) may draw advantages from the nodal downstaging effect and reduce the extent of axillary surgery with sentinel lymph node biopsy (SLNB) performed after NAST. Since there are concerns about low...
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Published in: | Breast cancer research and treatment 2017-05, Vol.163 (1), p.103-110 |
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creator | Zetterlund, Linda Holmstrand Frisell, Jan Zouzos, Athanasios Axelsson, Rimma Hatschek, Thomas de Boniface, Jana Celebioglu, Fuat |
description | Purpose
Patients with clinically node-positive breast cancer planned for neoadjuvant systemic therapy (NAST) may draw advantages from the nodal downstaging effect and reduce the extent of axillary surgery with sentinel lymph node biopsy (SLNB) performed after NAST. Since there are concerns about lower sentinel lymph node (SLN) detection and higher false-negative rates (FNR) in this setting, our aim was to define the accuracy of SLNB after NAST.
Methods
This Swedish national multicenter trial prospectively recruited 195 breast cancer patients from ten hospitals with T1–T4d biopsy-proven node-positive disease planned for NAST between October 1, 2010 and December 31, 2015. Clinically node-negative axillary status after NAST was not mandatory. SLNB was always attempted and followed by a completion axillary lymph node dissection (ALND).
Results
The SLN identification rate was 77.9% (152/195) but improved to 80.7% (138/171) with dual mapping. The median number of SLNs was two (range 1–5). A positive SLNB was found in 52% (79/152), almost 66% (52/79) of whom had additional positive non-sentinel lymph nodes. The overall pathologic nodal response rate was 33.3% (66/195). The overall FNR was 14.1% (13/92) but decreased to 4% (2/50) when only patients with two or more sentinel nodes were analyzed.
Conclusions
In biopsy-proven node-positive breast cancer, SLNB after NAST is feasible even though the identification rate is lower than in clinically node-negative patients. Since the overall FNR is unacceptably high, the omission of ALND should only be considered if two or more SLNs are identified. |
doi_str_mv | 10.1007/s10549-017-4164-1 |
format | article |
fullrecord | <record><control><sourceid>gale_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_498899</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A550951326</galeid><sourcerecordid>A550951326</sourcerecordid><originalsourceid>FETCH-LOGICAL-c759t-9e8874fef742c392900fddd44e13b561f7dcfe0b4605e2e1c3cab26e4ec057323</originalsourceid><addsrcrecordid>eNqNk81u1DAUhSMEoqXwAGyQJSTEJsV2nNjeIFUVf1IlFsDa8jg3My4eO9jOVPMmPC5OZ_oziEooi0TX3zm2T-6tqpcEnxKM-btEcMtkjQmvGelYTR5Vx6TlTc0p4Y-rY0w6XncCd0fVs5QuMcaSY_m0OqKCUtYIdlz9_nYFvU0rNMaQRjDZbgCtJ5etAZ8hohytdgg22k06W79EqdStB4fcdj2ukA89oIUNY9oiPcwKD0H3l9NG-4zSNmVYW4PyCqIet8h6ZJz11mjnttfiegzJXm-7iKBTRkZ7A_F59WTQLsGL_fuk-vHxw_fzz_XF109fzs8uasNbmWsJQnA2wMAZNY2kEuOh73vGgDSLtiMD780AeME63AIFYhqjF7QDBgaXpGhzUtU733QF47RQY7RrHbcqaKv2pZ_lCxSTQkhZePkgXzLs70Q3QtKUc3SE4aJ9v9MWYA39nHDU7tDiYMXblVqGjWobwXHTFYO3e4MYfk2QslrbZMA5XUKfkiJCEiFaTpr_QEsriJbQGX39F3oZpuhL6oUSHcXl3vSOWmoHyvohlCOa2VSdtS2WLWnofMLTf1Dl6ec2CB4GW-oHgjf3BCvQLq9ScFO2wadDkOxAUzo1RRhucyNYzeOgduOgyjioeRxK8CfVq_uB3ypu-r8AdP83y5JfQrx39Qdd_wBwdxmr</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1886208992</pqid></control><display><type>article</type><title>Swedish prospective multicenter trial evaluating sentinel lymph node biopsy after neoadjuvant systemic therapy in clinically node-positive breast cancer</title><source>Springer Link</source><creator>Zetterlund, Linda Holmstrand ; Frisell, Jan ; Zouzos, Athanasios ; Axelsson, Rimma ; Hatschek, Thomas ; de Boniface, Jana ; Celebioglu, Fuat</creator><creatorcontrib>Zetterlund, Linda Holmstrand ; Frisell, Jan ; Zouzos, Athanasios ; Axelsson, Rimma ; Hatschek, Thomas ; de Boniface, Jana ; Celebioglu, Fuat</creatorcontrib><description>Purpose
Patients with clinically node-positive breast cancer planned for neoadjuvant systemic therapy (NAST) may draw advantages from the nodal downstaging effect and reduce the extent of axillary surgery with sentinel lymph node biopsy (SLNB) performed after NAST. Since there are concerns about lower sentinel lymph node (SLN) detection and higher false-negative rates (FNR) in this setting, our aim was to define the accuracy of SLNB after NAST.
Methods
This Swedish national multicenter trial prospectively recruited 195 breast cancer patients from ten hospitals with T1–T4d biopsy-proven node-positive disease planned for NAST between October 1, 2010 and December 31, 2015. Clinically node-negative axillary status after NAST was not mandatory. SLNB was always attempted and followed by a completion axillary lymph node dissection (ALND).
Results
The SLN identification rate was 77.9% (152/195) but improved to 80.7% (138/171) with dual mapping. The median number of SLNs was two (range 1–5). A positive SLNB was found in 52% (79/152), almost 66% (52/79) of whom had additional positive non-sentinel lymph nodes. The overall pathologic nodal response rate was 33.3% (66/195). The overall FNR was 14.1% (13/92) but decreased to 4% (2/50) when only patients with two or more sentinel nodes were analyzed.
Conclusions
In biopsy-proven node-positive breast cancer, SLNB after NAST is feasible even though the identification rate is lower than in clinically node-negative patients. Since the overall FNR is unacceptably high, the omission of ALND should only be considered if two or more SLNs are identified.</description><identifier>ISSN: 0167-6806</identifier><identifier>ISSN: 1573-7217</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-017-4164-1</identifier><identifier>PMID: 28224384</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adjuvant chemotherapy ; Adult ; Aged ; Aged, 80 and over ; Anthracyclines - therapeutic use ; Aromatase Inhibitors - therapeutic use ; Axilla ; Biopsy ; Breast cancer ; Breast Neoplasms - therapy ; Cancer research ; Cancer therapies ; Clinical Trial ; Clinical trials ; Female ; Hospitals ; Humans ; Lymph node biopsy ; Lymph Node Excision - methods ; Lymphatic Metastasis ; Lymphatic system ; Mastectomy - methods ; Medicin och hälsovetenskap ; Medicine ; Medicine & Public Health ; Middle Aged ; Neoadjuvant Therapy ; Oncology ; Prospective Studies ; Sensitivity and Specificity ; Sentinel Lymph Node Biopsy - methods ; Sweden ; Taxoids - therapeutic use</subject><ispartof>Breast cancer research and treatment, 2017-05, Vol.163 (1), p.103-110</ispartof><rights>The Author(s) 2017</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Breast Cancer Research and Treatment is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c759t-9e8874fef742c392900fddd44e13b561f7dcfe0b4605e2e1c3cab26e4ec057323</citedby><cites>FETCH-LOGICAL-c759t-9e8874fef742c392900fddd44e13b561f7dcfe0b4605e2e1c3cab26e4ec057323</cites><orcidid>0000-0002-4774-5945</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28224384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:135616140$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Zetterlund, Linda Holmstrand</creatorcontrib><creatorcontrib>Frisell, Jan</creatorcontrib><creatorcontrib>Zouzos, Athanasios</creatorcontrib><creatorcontrib>Axelsson, Rimma</creatorcontrib><creatorcontrib>Hatschek, Thomas</creatorcontrib><creatorcontrib>de Boniface, Jana</creatorcontrib><creatorcontrib>Celebioglu, Fuat</creatorcontrib><title>Swedish prospective multicenter trial evaluating sentinel lymph node biopsy after neoadjuvant systemic therapy in clinically node-positive breast cancer</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose
Patients with clinically node-positive breast cancer planned for neoadjuvant systemic therapy (NAST) may draw advantages from the nodal downstaging effect and reduce the extent of axillary surgery with sentinel lymph node biopsy (SLNB) performed after NAST. Since there are concerns about lower sentinel lymph node (SLN) detection and higher false-negative rates (FNR) in this setting, our aim was to define the accuracy of SLNB after NAST.
Methods
This Swedish national multicenter trial prospectively recruited 195 breast cancer patients from ten hospitals with T1–T4d biopsy-proven node-positive disease planned for NAST between October 1, 2010 and December 31, 2015. Clinically node-negative axillary status after NAST was not mandatory. SLNB was always attempted and followed by a completion axillary lymph node dissection (ALND).
Results
The SLN identification rate was 77.9% (152/195) but improved to 80.7% (138/171) with dual mapping. The median number of SLNs was two (range 1–5). A positive SLNB was found in 52% (79/152), almost 66% (52/79) of whom had additional positive non-sentinel lymph nodes. The overall pathologic nodal response rate was 33.3% (66/195). The overall FNR was 14.1% (13/92) but decreased to 4% (2/50) when only patients with two or more sentinel nodes were analyzed.
Conclusions
In biopsy-proven node-positive breast cancer, SLNB after NAST is feasible even though the identification rate is lower than in clinically node-negative patients. Since the overall FNR is unacceptably high, the omission of ALND should only be considered if two or more SLNs are identified.</description><subject>Adjuvant chemotherapy</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anthracyclines - therapeutic use</subject><subject>Aromatase Inhibitors - therapeutic use</subject><subject>Axilla</subject><subject>Biopsy</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - therapy</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Clinical Trial</subject><subject>Clinical trials</subject><subject>Female</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Lymph node biopsy</subject><subject>Lymph Node Excision - methods</subject><subject>Lymphatic Metastasis</subject><subject>Lymphatic system</subject><subject>Mastectomy - methods</subject><subject>Medicin och hälsovetenskap</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>Oncology</subject><subject>Prospective Studies</subject><subject>Sensitivity and Specificity</subject><subject>Sentinel Lymph Node Biopsy - methods</subject><subject>Sweden</subject><subject>Taxoids - therapeutic use</subject><issn>0167-6806</issn><issn>1573-7217</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNk81u1DAUhSMEoqXwAGyQJSTEJsV2nNjeIFUVf1IlFsDa8jg3My4eO9jOVPMmPC5OZ_oziEooi0TX3zm2T-6tqpcEnxKM-btEcMtkjQmvGelYTR5Vx6TlTc0p4Y-rY0w6XncCd0fVs5QuMcaSY_m0OqKCUtYIdlz9_nYFvU0rNMaQRjDZbgCtJ5etAZ8hohytdgg22k06W79EqdStB4fcdj2ukA89oIUNY9oiPcwKD0H3l9NG-4zSNmVYW4PyCqIet8h6ZJz11mjnttfiegzJXm-7iKBTRkZ7A_F59WTQLsGL_fuk-vHxw_fzz_XF109fzs8uasNbmWsJQnA2wMAZNY2kEuOh73vGgDSLtiMD780AeME63AIFYhqjF7QDBgaXpGhzUtU733QF47RQY7RrHbcqaKv2pZ_lCxSTQkhZePkgXzLs70Q3QtKUc3SE4aJ9v9MWYA39nHDU7tDiYMXblVqGjWobwXHTFYO3e4MYfk2QslrbZMA5XUKfkiJCEiFaTpr_QEsriJbQGX39F3oZpuhL6oUSHcXl3vSOWmoHyvohlCOa2VSdtS2WLWnofMLTf1Dl6ec2CB4GW-oHgjf3BCvQLq9ScFO2wadDkOxAUzo1RRhucyNYzeOgduOgyjioeRxK8CfVq_uB3ypu-r8AdP83y5JfQrx39Qdd_wBwdxmr</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Zetterlund, Linda Holmstrand</creator><creator>Frisell, Jan</creator><creator>Zouzos, Athanasios</creator><creator>Axelsson, Rimma</creator><creator>Hatschek, Thomas</creator><creator>de Boniface, Jana</creator><creator>Celebioglu, Fuat</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</scope><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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-4774-5945</orcidid></search><sort><creationdate>20170501</creationdate><title>Swedish prospective multicenter trial evaluating sentinel lymph node biopsy after neoadjuvant systemic therapy in clinically node-positive breast cancer</title><author>Zetterlund, Linda Holmstrand ; Frisell, Jan ; Zouzos, Athanasios ; Axelsson, Rimma ; Hatschek, Thomas ; de Boniface, Jana ; Celebioglu, Fuat</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c759t-9e8874fef742c392900fddd44e13b561f7dcfe0b4605e2e1c3cab26e4ec057323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adjuvant chemotherapy</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anthracyclines - therapeutic use</topic><topic>Aromatase Inhibitors - therapeutic use</topic><topic>Axilla</topic><topic>Biopsy</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - therapy</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Clinical Trial</topic><topic>Clinical trials</topic><topic>Female</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Lymph node biopsy</topic><topic>Lymph Node Excision - methods</topic><topic>Lymphatic Metastasis</topic><topic>Lymphatic system</topic><topic>Mastectomy - methods</topic><topic>Medicin och hälsovetenskap</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>Oncology</topic><topic>Prospective Studies</topic><topic>Sensitivity and Specificity</topic><topic>Sentinel Lymph Node Biopsy - methods</topic><topic>Sweden</topic><topic>Taxoids - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zetterlund, Linda Holmstrand</creatorcontrib><creatorcontrib>Frisell, Jan</creatorcontrib><creatorcontrib>Zouzos, Athanasios</creatorcontrib><creatorcontrib>Axelsson, Rimma</creatorcontrib><creatorcontrib>Hatschek, Thomas</creatorcontrib><creatorcontrib>de Boniface, Jana</creatorcontrib><creatorcontrib>Celebioglu, Fuat</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zetterlund, Linda Holmstrand</au><au>Frisell, Jan</au><au>Zouzos, Athanasios</au><au>Axelsson, Rimma</au><au>Hatschek, Thomas</au><au>de Boniface, Jana</au><au>Celebioglu, Fuat</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Swedish prospective multicenter trial evaluating sentinel lymph node biopsy after neoadjuvant systemic therapy in clinically node-positive breast cancer</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>163</volume><issue>1</issue><spage>103</spage><epage>110</epage><pages>103-110</pages><issn>0167-6806</issn><issn>1573-7217</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>Purpose
Patients with clinically node-positive breast cancer planned for neoadjuvant systemic therapy (NAST) may draw advantages from the nodal downstaging effect and reduce the extent of axillary surgery with sentinel lymph node biopsy (SLNB) performed after NAST. Since there are concerns about lower sentinel lymph node (SLN) detection and higher false-negative rates (FNR) in this setting, our aim was to define the accuracy of SLNB after NAST.
Methods
This Swedish national multicenter trial prospectively recruited 195 breast cancer patients from ten hospitals with T1–T4d biopsy-proven node-positive disease planned for NAST between October 1, 2010 and December 31, 2015. Clinically node-negative axillary status after NAST was not mandatory. SLNB was always attempted and followed by a completion axillary lymph node dissection (ALND).
Results
The SLN identification rate was 77.9% (152/195) but improved to 80.7% (138/171) with dual mapping. The median number of SLNs was two (range 1–5). A positive SLNB was found in 52% (79/152), almost 66% (52/79) of whom had additional positive non-sentinel lymph nodes. The overall pathologic nodal response rate was 33.3% (66/195). The overall FNR was 14.1% (13/92) but decreased to 4% (2/50) when only patients with two or more sentinel nodes were analyzed.
Conclusions
In biopsy-proven node-positive breast cancer, SLNB after NAST is feasible even though the identification rate is lower than in clinically node-negative patients. Since the overall FNR is unacceptably high, the omission of ALND should only be considered if two or more SLNs are identified.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>28224384</pmid><doi>10.1007/s10549-017-4164-1</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4774-5945</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvant chemotherapy Adult Aged Aged, 80 and over Anthracyclines - therapeutic use Aromatase Inhibitors - therapeutic use Axilla Biopsy Breast cancer Breast Neoplasms - therapy Cancer research Cancer therapies Clinical Trial Clinical trials Female Hospitals Humans Lymph node biopsy Lymph Node Excision - methods Lymphatic Metastasis Lymphatic system Mastectomy - methods Medicin och hälsovetenskap Medicine Medicine & Public Health Middle Aged Neoadjuvant Therapy Oncology Prospective Studies Sensitivity and Specificity Sentinel Lymph Node Biopsy - methods Sweden Taxoids - therapeutic use |
title | Swedish prospective multicenter trial evaluating sentinel lymph node biopsy after neoadjuvant systemic therapy in clinically node-positive breast cancer |
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