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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
Main Authors: Zetterlund, Linda Holmstrand, Frisell, Jan, Zouzos, Athanasios, Axelsson, Rimma, Hatschek, Thomas, de Boniface, Jana, Celebioglu, Fuat
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container_title Breast cancer research and treatment
container_volume 163
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
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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 &amp; 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. 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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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