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Sentinel Lymph Node Biopsy in Thin Cutaneous Melanoma: A Systematic Review and Meta-Analysis

Background Most patients with melanoma have a thin (≤1.00 mm) lesion. There is uncertainty as to which patients with thin melanoma should undergo sentinel lymph node (SN) biopsy. We sought to quantify the proportion of SN metastases in patients with thin melanoma and to determine the pooled effect o...

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Published in:Annals of surgical oncology 2016-12, Vol.23 (13), p.4178-4188
Main Authors: Cordeiro, Erin, Gervais, Mai-Kim, Shah, Prakesh S., Look Hong, Nicole J., Wright, Frances C.
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Gervais, Mai-Kim
Shah, Prakesh S.
Look Hong, Nicole J.
Wright, Frances C.
description Background Most patients with melanoma have a thin (≤1.00 mm) lesion. There is uncertainty as to which patients with thin melanoma should undergo sentinel lymph node (SN) biopsy. We sought to quantify the proportion of SN metastases in patients with thin melanoma and to determine the pooled effect of high-risk features of the primary lesion on SN positivity. Methods Published literature between 1980 and 2015 was searched and critically appraised. Primary outcome was the proportion of SN metastases in patients with thin cutaneous melanoma. Secondary outcomes included the effect of high-risk pathological features of the primary lesion on the proportion of SN metastases. Summary measures were estimated by Mantel–Haenszel method using random effects meta-analyses. Results Sixty studies (10,928 patients) met the criteria for inclusion. Pooled SN positivity was 4.5 % [95 % confidence interval (CI) 3.8–5.2 %]. Predictors of a positive SN were: thickness ≥0.75 mm [adjusted odds ratio (AOR) 1.90 (95 % CI 1.08–3.34); with a likelihood of SN metastases of 8.8 % (95 % CI 6.4–11.2 %)]; Clark level IV/V [AOR 2.24 (95 % CI 1.23–4.08); with a likelihood of 7.3 % (95 % CI 6.2–8.4 %)]; ≥1 mitoses/mm 2 [AOR 6.64 (95 % CI 2.77–15.88); pooled likelihood 8.8 % (95 % CI 6.2–11.4 %)]; and the presence of microsatellites [unadjusted OR 6.94 (95 % CI 2.13–22.60); likelihood 26.6 % (95 % CI 4.3–48.9 %)]. Conclusions The pooled proportion of SN metastases in thin melanoma is 4.5 %. Thickness ≥0.75 mm, Clark level IV/V, mitoses, and microsatellites significantly increased the odds of SN positivity and should prompt strong consideration of SN biopsy.
doi_str_mv 10.1245/s10434-016-5137-z
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There is uncertainty as to which patients with thin melanoma should undergo sentinel lymph node (SN) biopsy. We sought to quantify the proportion of SN metastases in patients with thin melanoma and to determine the pooled effect of high-risk features of the primary lesion on SN positivity. Methods Published literature between 1980 and 2015 was searched and critically appraised. Primary outcome was the proportion of SN metastases in patients with thin cutaneous melanoma. Secondary outcomes included the effect of high-risk pathological features of the primary lesion on the proportion of SN metastases. Summary measures were estimated by Mantel–Haenszel method using random effects meta-analyses. Results Sixty studies (10,928 patients) met the criteria for inclusion. Pooled SN positivity was 4.5 % [95 % confidence interval (CI) 3.8–5.2 %]. Predictors of a positive SN were: thickness ≥0.75 mm [adjusted odds ratio (AOR) 1.90 (95 % CI 1.08–3.34); with a likelihood of SN metastases of 8.8 % (95 % CI 6.4–11.2 %)]; Clark level IV/V [AOR 2.24 (95 % CI 1.23–4.08); with a likelihood of 7.3 % (95 % CI 6.2–8.4 %)]; ≥1 mitoses/mm 2 [AOR 6.64 (95 % CI 2.77–15.88); pooled likelihood 8.8 % (95 % CI 6.2–11.4 %)]; and the presence of microsatellites [unadjusted OR 6.94 (95 % CI 2.13–22.60); likelihood 26.6 % (95 % CI 4.3–48.9 %)]. Conclusions The pooled proportion of SN metastases in thin melanoma is 4.5 %. Thickness ≥0.75 mm, Clark level IV/V, mitoses, and microsatellites significantly increased the odds of SN positivity and should prompt strong consideration of SN biopsy.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-016-5137-z</identifier><identifier>PMID: 26932710</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Humans ; Lymph Nodes - pathology ; Lymphatic Metastasis ; Medicine ; Medicine &amp; Public Health ; Melanoma - pathology ; Melanoma - secondary ; Melanomas ; Mitotic Index ; Oncology ; Patient Selection ; Risk Factors ; Sentinel Lymph Node Biopsy ; Skin Neoplasms - pathology ; Surgery ; Surgical Oncology ; Tumor Burden</subject><ispartof>Annals of surgical oncology, 2016-12, Vol.23 (13), p.4178-4188</ispartof><rights>Society of Surgical Oncology 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-68e530a4cdfe5406130f2fd8b87d56512a787f268b0953ae59460c1ab834c23e3</citedby><cites>FETCH-LOGICAL-c372t-68e530a4cdfe5406130f2fd8b87d56512a787f268b0953ae59460c1ab834c23e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26932710$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cordeiro, Erin</creatorcontrib><creatorcontrib>Gervais, Mai-Kim</creatorcontrib><creatorcontrib>Shah, Prakesh S.</creatorcontrib><creatorcontrib>Look Hong, Nicole J.</creatorcontrib><creatorcontrib>Wright, Frances C.</creatorcontrib><title>Sentinel Lymph Node Biopsy in Thin Cutaneous Melanoma: A Systematic Review and Meta-Analysis</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><addtitle>Ann Surg Oncol</addtitle><description>Background Most patients with melanoma have a thin (≤1.00 mm) lesion. There is uncertainty as to which patients with thin melanoma should undergo sentinel lymph node (SN) biopsy. We sought to quantify the proportion of SN metastases in patients with thin melanoma and to determine the pooled effect of high-risk features of the primary lesion on SN positivity. Methods Published literature between 1980 and 2015 was searched and critically appraised. Primary outcome was the proportion of SN metastases in patients with thin cutaneous melanoma. Secondary outcomes included the effect of high-risk pathological features of the primary lesion on the proportion of SN metastases. Summary measures were estimated by Mantel–Haenszel method using random effects meta-analyses. Results Sixty studies (10,928 patients) met the criteria for inclusion. Pooled SN positivity was 4.5 % [95 % confidence interval (CI) 3.8–5.2 %]. Predictors of a positive SN were: thickness ≥0.75 mm [adjusted odds ratio (AOR) 1.90 (95 % CI 1.08–3.34); with a likelihood of SN metastases of 8.8 % (95 % CI 6.4–11.2 %)]; Clark level IV/V [AOR 2.24 (95 % CI 1.23–4.08); with a likelihood of 7.3 % (95 % CI 6.2–8.4 %)]; ≥1 mitoses/mm 2 [AOR 6.64 (95 % CI 2.77–15.88); pooled likelihood 8.8 % (95 % CI 6.2–11.4 %)]; and the presence of microsatellites [unadjusted OR 6.94 (95 % CI 2.13–22.60); likelihood 26.6 % (95 % CI 4.3–48.9 %)]. Conclusions The pooled proportion of SN metastases in thin melanoma is 4.5 %. Thickness ≥0.75 mm, Clark level IV/V, mitoses, and microsatellites significantly increased the odds of SN positivity and should prompt strong consideration of SN biopsy.</description><subject>Humans</subject><subject>Lymph Nodes - pathology</subject><subject>Lymphatic Metastasis</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Melanoma - pathology</subject><subject>Melanoma - secondary</subject><subject>Melanomas</subject><subject>Mitotic Index</subject><subject>Oncology</subject><subject>Patient Selection</subject><subject>Risk Factors</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Skin Neoplasms - pathology</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Tumor Burden</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1kF1LwzAUhoMobk5_gDcS8Mabar6beTeHXzAV3LwTQtaeuo5-zKZVul9vRqeI4E1OyHnOm8OD0DEl55QJeeEoEVwEhKpAUh4G6x3Up9K_CKXprr8TpYMhU7KHDpxbEkJDTuQ-6jE15CykpI9ep1DUaQEZnrT5aoEfyxjwVVquXIvTAs8W_hg3tS2gbBx-gMwWZW4v8QhPW1dDbus0ws_wkcIntkXsidoGo8JmrUvdIdpLbObgaFsH6OXmeja-CyZPt_fj0SSIeMjqQGmQnFgRxQlIQRTlJGFJrOc6jKWSlNlQhwlTek6GkluQQ6FIRO1ccxExDnyAzrrcVVW-N-Bqk6cugizr1jZUM6WUkIR59PQPuiybyu-7obgIpaZyQ9GOiqrSuQoSs6rS3FatocRs1JtOvfHqzUa9WfuZk21yM88h_pn4du0B1gHOt4o3qH59_W_qF93QjTM</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Cordeiro, Erin</creator><creator>Gervais, Mai-Kim</creator><creator>Shah, Prakesh S.</creator><creator>Look Hong, Nicole J.</creator><creator>Wright, Frances C.</creator><general>Springer International Publishing</general><general>Springer Nature B.V</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20161201</creationdate><title>Sentinel Lymph Node Biopsy in Thin Cutaneous Melanoma: A Systematic Review and Meta-Analysis</title><author>Cordeiro, Erin ; Gervais, Mai-Kim ; Shah, Prakesh S. ; Look Hong, Nicole J. ; Wright, Frances C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-68e530a4cdfe5406130f2fd8b87d56512a787f268b0953ae59460c1ab834c23e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Humans</topic><topic>Lymph Nodes - pathology</topic><topic>Lymphatic Metastasis</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Melanoma - pathology</topic><topic>Melanoma - secondary</topic><topic>Melanomas</topic><topic>Mitotic Index</topic><topic>Oncology</topic><topic>Patient Selection</topic><topic>Risk Factors</topic><topic>Sentinel Lymph Node Biopsy</topic><topic>Skin Neoplasms - pathology</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Tumor Burden</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cordeiro, Erin</creatorcontrib><creatorcontrib>Gervais, Mai-Kim</creatorcontrib><creatorcontrib>Shah, Prakesh S.</creatorcontrib><creatorcontrib>Look Hong, Nicole J.</creatorcontrib><creatorcontrib>Wright, Frances C.</creatorcontrib><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>ProQuest Health &amp; 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There is uncertainty as to which patients with thin melanoma should undergo sentinel lymph node (SN) biopsy. We sought to quantify the proportion of SN metastases in patients with thin melanoma and to determine the pooled effect of high-risk features of the primary lesion on SN positivity. Methods Published literature between 1980 and 2015 was searched and critically appraised. Primary outcome was the proportion of SN metastases in patients with thin cutaneous melanoma. Secondary outcomes included the effect of high-risk pathological features of the primary lesion on the proportion of SN metastases. Summary measures were estimated by Mantel–Haenszel method using random effects meta-analyses. Results Sixty studies (10,928 patients) met the criteria for inclusion. Pooled SN positivity was 4.5 % [95 % confidence interval (CI) 3.8–5.2 %]. Predictors of a positive SN were: thickness ≥0.75 mm [adjusted odds ratio (AOR) 1.90 (95 % CI 1.08–3.34); with a likelihood of SN metastases of 8.8 % (95 % CI 6.4–11.2 %)]; Clark level IV/V [AOR 2.24 (95 % CI 1.23–4.08); with a likelihood of 7.3 % (95 % CI 6.2–8.4 %)]; ≥1 mitoses/mm 2 [AOR 6.64 (95 % CI 2.77–15.88); pooled likelihood 8.8 % (95 % CI 6.2–11.4 %)]; and the presence of microsatellites [unadjusted OR 6.94 (95 % CI 2.13–22.60); likelihood 26.6 % (95 % CI 4.3–48.9 %)]. Conclusions The pooled proportion of SN metastases in thin melanoma is 4.5 %. Thickness ≥0.75 mm, Clark level IV/V, mitoses, and microsatellites significantly increased the odds of SN positivity and should prompt strong consideration of SN biopsy.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>26932710</pmid><doi>10.1245/s10434-016-5137-z</doi><tpages>11</tpages></addata></record>
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subjects Humans
Lymph Nodes - pathology
Lymphatic Metastasis
Medicine
Medicine & Public Health
Melanoma - pathology
Melanoma - secondary
Melanomas
Mitotic Index
Oncology
Patient Selection
Risk Factors
Sentinel Lymph Node Biopsy
Skin Neoplasms - pathology
Surgery
Surgical Oncology
Tumor Burden
title Sentinel Lymph Node Biopsy in Thin Cutaneous Melanoma: A Systematic Review and Meta-Analysis
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