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The Feasibility and Accuracy of Sentinel Lymph Node Biopsy in Initially Clinically Node-Negative Breast Cancer after Neoadjuvant Chemotherapy: A Systematic Review and Meta-Analysis
With the increased use of neoadjuvant chemotherapy (NAC) in breast cancer, the timing of sentinel lymph node biopsy (SLNB) has become increasingly important. In this study, we aimed to evaluate the feasibility and accuracy of SLNB for initially clinically node-negative breast cancer after NAC by con...
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Published in: | PloS one 2016-09, Vol.11 (9), p.e0162605-e0162605 |
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description | With the increased use of neoadjuvant chemotherapy (NAC) in breast cancer, the timing of sentinel lymph node biopsy (SLNB) has become increasingly important. In this study, we aimed to evaluate the feasibility and accuracy of SLNB for initially clinically node-negative breast cancer after NAC by conducting a systematic review and meta-analysis.
We searched PubMed, Embase, and the Cochrane Library from January 1, 1993 to November 30, 2015 for studies on initially clinically node-negative breast cancer patients who underwent SLNB after NAC followed by axillary lymph node dissection (ALND).
A total of 1,456 patients from 16 studies were included in this review. The pooled identification rate (IR) for SLNB was 96% [95% confidence interval (CI): 95%-97%], and the false negative rate (FNR) was 6% (95% CI: 3%-8%). The pooled sensitivity, negative predictive value (NPV) and accuracy rate (AR) were 94% (95% CI: 92%-97%, I2 = 27.5%), 98% (95% CI: 98%-99%, I2 = 42.7%) and 99% (95% CI: 99%-100%, I2 = 32.6%), respectively. In the subgroup analysis, no significant differences were found in either the IR of an SLNB when different mapping methods were used (P = 0.180) or in the FNR between studies with and without immunohistochemistry (IHC) staining (P = 0.241).
Based on current evidence, SLNB is technically feasible and accurate enough for axillary staging in initially clinically node-negative breast cancer patients after NAC. |
doi_str_mv | 10.1371/journal.pone.0162605 |
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We searched PubMed, Embase, and the Cochrane Library from January 1, 1993 to November 30, 2015 for studies on initially clinically node-negative breast cancer patients who underwent SLNB after NAC followed by axillary lymph node dissection (ALND).
A total of 1,456 patients from 16 studies were included in this review. The pooled identification rate (IR) for SLNB was 96% [95% confidence interval (CI): 95%-97%], and the false negative rate (FNR) was 6% (95% CI: 3%-8%). The pooled sensitivity, negative predictive value (NPV) and accuracy rate (AR) were 94% (95% CI: 92%-97%, I2 = 27.5%), 98% (95% CI: 98%-99%, I2 = 42.7%) and 99% (95% CI: 99%-100%, I2 = 32.6%), respectively. In the subgroup analysis, no significant differences were found in either the IR of an SLNB when different mapping methods were used (P = 0.180) or in the FNR between studies with and without immunohistochemistry (IHC) staining (P = 0.241).
Based on current evidence, SLNB is technically feasible and accurate enough for axillary staging in initially clinically node-negative breast cancer patients after NAC.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0162605</identifier><identifier>PMID: 27606623</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adjuvant chemotherapy ; Biology and Life Sciences ; Biopsy ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; Cancer ; Cancer research ; Chemotherapy ; Confidence intervals ; False Negative Reactions ; Feasibility Studies ; Female ; Humans ; Immunohistochemistry ; Infrared radiation ; Lymph ; Lymph node biopsy ; Lymph nodes ; Lymph Nodes - pathology ; Lymphatic Metastasis - pathology ; Mastectomy ; Medical ethics ; Medicine and Health Sciences ; Meta-analysis ; Neoadjuvant Therapy ; Patients ; Physical Sciences ; Predictive Value of Tests ; Publication Bias ; Research and Analysis Methods ; Sentinel Lymph Node Biopsy ; Systematic review</subject><ispartof>PloS one, 2016-09, Vol.11 (9), p.e0162605-e0162605</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Geng et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Geng et al 2016 Geng et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c725t-d34bdfcd58313f70d6068febdd14e0e84e457cb6e773140c65b83ff4b6811c7c3</citedby><cites>FETCH-LOGICAL-c725t-d34bdfcd58313f70d6068febdd14e0e84e457cb6e773140c65b83ff4b6811c7c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1817860828/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1817860828?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27606623$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Dolcetti, Riccardo</contributor><creatorcontrib>Geng, Chong</creatorcontrib><creatorcontrib>Chen, Xiao</creatorcontrib><creatorcontrib>Pan, Xiaohua</creatorcontrib><creatorcontrib>Li, Jiyu</creatorcontrib><title>The Feasibility and Accuracy of Sentinel Lymph Node Biopsy in Initially Clinically Node-Negative Breast Cancer after Neoadjuvant Chemotherapy: A Systematic Review and Meta-Analysis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>With the increased use of neoadjuvant chemotherapy (NAC) in breast cancer, the timing of sentinel lymph node biopsy (SLNB) has become increasingly important. In this study, we aimed to evaluate the feasibility and accuracy of SLNB for initially clinically node-negative breast cancer after NAC by conducting a systematic review and meta-analysis.
We searched PubMed, Embase, and the Cochrane Library from January 1, 1993 to November 30, 2015 for studies on initially clinically node-negative breast cancer patients who underwent SLNB after NAC followed by axillary lymph node dissection (ALND).
A total of 1,456 patients from 16 studies were included in this review. The pooled identification rate (IR) for SLNB was 96% [95% confidence interval (CI): 95%-97%], and the false negative rate (FNR) was 6% (95% CI: 3%-8%). The pooled sensitivity, negative predictive value (NPV) and accuracy rate (AR) were 94% (95% CI: 92%-97%, I2 = 27.5%), 98% (95% CI: 98%-99%, I2 = 42.7%) and 99% (95% CI: 99%-100%, I2 = 32.6%), respectively. In the subgroup analysis, no significant differences were found in either the IR of an SLNB when different mapping methods were used (P = 0.180) or in the FNR between studies with and without immunohistochemistry (IHC) staining (P = 0.241).
Based on current evidence, SLNB is technically feasible and accurate enough for axillary staging in initially clinically node-negative breast cancer patients after NAC.</description><subject>Adjuvant chemotherapy</subject><subject>Biology and Life Sciences</subject><subject>Biopsy</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer</subject><subject>Cancer research</subject><subject>Chemotherapy</subject><subject>Confidence intervals</subject><subject>False Negative Reactions</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Infrared radiation</subject><subject>Lymph</subject><subject>Lymph node biopsy</subject><subject>Lymph nodes</subject><subject>Lymph Nodes - pathology</subject><subject>Lymphatic Metastasis - pathology</subject><subject>Mastectomy</subject><subject>Medical ethics</subject><subject>Medicine and Health Sciences</subject><subject>Meta-analysis</subject><subject>Neoadjuvant Therapy</subject><subject>Patients</subject><subject>Physical Sciences</subject><subject>Predictive Value of Tests</subject><subject>Publication Bias</subject><subject>Research and Analysis Methods</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Systematic review</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9Fu0zAUhiMEYmPwBggsISG4aLHjxHa5QCoVg0pjk7bBreU4J60rxy6xU8h78YC4WzetaBdTJMeyv__3Occ-WfaS4DGhnHxY-b5zyo7X3sEYE5YzXD7KDsmE5iOWY_r4zvwgexbCCuOSCsaeZgc5Z5ixnB5mfy-XgI5BBVMZa-KAlKvRVOu-U3pAvkEX4KJxYNHJ0K6X6NTXgD4bvw4DMg7NnYlGWTugmTXO6KvplhmdwkJFs0lwl9wjmimnoUOqiWk8Ba_qVb9RLm0sofVxCZ1aDx_RFF0MIUKbtBqdw8bA76uQvkNUo2nKdwgmPM-eNMoGeLH7H2U_jr9czr6NTs6-zmfTk5HmeRlHNS2qutF1KSihDcd1Slo0UNU1KQCDKKAoua4YcE5JgTUrK0GbpqiYIERzTY-y19e-a-uD3BU8SCIIFwyLXCRifk3UXq3kujOt6gbplZFXC75bSNWlVCxIpoGLErRuCl4wTYWqKCl5Scq81HlTJa9Pu9P6qoVap8J3yu6Z7u84s5QLv5ElJuWE4WTwbmfQ-V89hChbEzRYqxz4fht3zoXggrMHoERQOiE8T-ib_9D7C7GjFirlalzjU4h6ayqnBceTgrDJ1mt8D5W-Glqj00NuTFrfE7zfEyQmwp-4UH0Icn5x_nD27Oc--_YOuwRl4zJ420fjXdgHi2tQdz6EDprb-yBYbvvwphpy24dy14dJ9uruXd6KbhqP_gNeYi9P</recordid><startdate>20160908</startdate><enddate>20160908</enddate><creator>Geng, Chong</creator><creator>Chen, Xiao</creator><creator>Pan, Xiaohua</creator><creator>Li, Jiyu</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160908</creationdate><title>The Feasibility and Accuracy of Sentinel Lymph Node Biopsy in Initially Clinically Node-Negative Breast Cancer after Neoadjuvant Chemotherapy: A Systematic Review and Meta-Analysis</title><author>Geng, Chong ; Chen, Xiao ; Pan, Xiaohua ; Li, Jiyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c725t-d34bdfcd58313f70d6068febdd14e0e84e457cb6e773140c65b83ff4b6811c7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adjuvant chemotherapy</topic><topic>Biology and Life Sciences</topic><topic>Biopsy</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Geng, Chong</au><au>Chen, Xiao</au><au>Pan, Xiaohua</au><au>Li, Jiyu</au><au>Dolcetti, Riccardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Feasibility and Accuracy of Sentinel Lymph Node Biopsy in Initially Clinically Node-Negative Breast Cancer after Neoadjuvant Chemotherapy: A Systematic Review and Meta-Analysis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-09-08</date><risdate>2016</risdate><volume>11</volume><issue>9</issue><spage>e0162605</spage><epage>e0162605</epage><pages>e0162605-e0162605</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>With the increased use of neoadjuvant chemotherapy (NAC) in breast cancer, the timing of sentinel lymph node biopsy (SLNB) has become increasingly important. In this study, we aimed to evaluate the feasibility and accuracy of SLNB for initially clinically node-negative breast cancer after NAC by conducting a systematic review and meta-analysis.
We searched PubMed, Embase, and the Cochrane Library from January 1, 1993 to November 30, 2015 for studies on initially clinically node-negative breast cancer patients who underwent SLNB after NAC followed by axillary lymph node dissection (ALND).
A total of 1,456 patients from 16 studies were included in this review. The pooled identification rate (IR) for SLNB was 96% [95% confidence interval (CI): 95%-97%], and the false negative rate (FNR) was 6% (95% CI: 3%-8%). The pooled sensitivity, negative predictive value (NPV) and accuracy rate (AR) were 94% (95% CI: 92%-97%, I2 = 27.5%), 98% (95% CI: 98%-99%, I2 = 42.7%) and 99% (95% CI: 99%-100%, I2 = 32.6%), respectively. In the subgroup analysis, no significant differences were found in either the IR of an SLNB when different mapping methods were used (P = 0.180) or in the FNR between studies with and without immunohistochemistry (IHC) staining (P = 0.241).
Based on current evidence, SLNB is technically feasible and accurate enough for axillary staging in initially clinically node-negative breast cancer patients after NAC.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27606623</pmid><doi>10.1371/journal.pone.0162605</doi><tpages>e0162605</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvant chemotherapy Biology and Life Sciences Biopsy Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - pathology Cancer Cancer research Chemotherapy Confidence intervals False Negative Reactions Feasibility Studies Female Humans Immunohistochemistry Infrared radiation Lymph Lymph node biopsy Lymph nodes Lymph Nodes - pathology Lymphatic Metastasis - pathology Mastectomy Medical ethics Medicine and Health Sciences Meta-analysis Neoadjuvant Therapy Patients Physical Sciences Predictive Value of Tests Publication Bias Research and Analysis Methods Sentinel Lymph Node Biopsy Systematic review |
title | The Feasibility and Accuracy of Sentinel Lymph Node Biopsy in Initially Clinically Node-Negative Breast Cancer after Neoadjuvant Chemotherapy: A Systematic Review and Meta-Analysis |
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