Is Head and Neck Melanoma Different from Trunk and Extremity Melanomas with Respect to Sentinel Lymph Node Status and Clinical Outcome?

Background Previous studies showed conflicting and inconsistent results regarding the effect of anatomic location of the melanoma on sentinel lymph node (SLN) positivity and/or survival. This study was conducted to evaluate and compare the effect of the anatomic locations of primary melanoma on long...

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Veröffentlicht in:Annals of surgical oncology 2013-09, Vol.20 (9), p.3089-3097
Hauptverfasser: Fadaki, Niloofar, Li, Rui, Parrett, Brian, Sanders, Grant, Thummala, Suresh, Martineau, Lea, Cardona-Huerta, Servando, Miranda, Suzette, Cheng, Shih-Tsung, Miller, James R., Singer, Mark, Cleaver, James E., Kashani-Sabet, Mohammed, Leong, Stanley P. L.
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container_end_page 3097
container_issue 9
container_start_page 3089
container_title Annals of surgical oncology
container_volume 20
creator Fadaki, Niloofar
Li, Rui
Parrett, Brian
Sanders, Grant
Thummala, Suresh
Martineau, Lea
Cardona-Huerta, Servando
Miranda, Suzette
Cheng, Shih-Tsung
Miller, James R.
Singer, Mark
Cleaver, James E.
Kashani-Sabet, Mohammed
Leong, Stanley P. L.
description Background Previous studies showed conflicting and inconsistent results regarding the effect of anatomic location of the melanoma on sentinel lymph node (SLN) positivity and/or survival. This study was conducted to evaluate and compare the effect of the anatomic locations of primary melanoma on long-term clinical outcomes. Methods All consecutive cutaneous melanoma patients ( n  = 2,079) who underwent selective SLN dissection (SLND) from 1993 to 2009 in a single academic tertiary-care medical center were included. SLN positive rate, disease-free survival (DFS), and overall survival (OS) were determined. Kaplan-Meier survival, univariate, and multivariate analyses were performed to determine predictive factors for SLN status, DFS, and OS. Results Head and neck melanoma (HNM) had the lowest SLN-positive rate at 10.8 % (16.8 % for extremity and 19.3 % for trunk; P  = 0.002) but had the worst 5-year DFS ( P  
doi_str_mv 10.1245/s10434-013-2977-7
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L.</creator><creatorcontrib>Fadaki, Niloofar ; Li, Rui ; Parrett, Brian ; Sanders, Grant ; Thummala, Suresh ; Martineau, Lea ; Cardona-Huerta, Servando ; Miranda, Suzette ; Cheng, Shih-Tsung ; Miller, James R. ; Singer, Mark ; Cleaver, James E. ; Kashani-Sabet, Mohammed ; Leong, Stanley P. L.</creatorcontrib><description><![CDATA[Background Previous studies showed conflicting and inconsistent results regarding the effect of anatomic location of the melanoma on sentinel lymph node (SLN) positivity and/or survival. This study was conducted to evaluate and compare the effect of the anatomic locations of primary melanoma on long-term clinical outcomes. Methods All consecutive cutaneous melanoma patients ( n  = 2,079) who underwent selective SLN dissection (SLND) from 1993 to 2009 in a single academic tertiary-care medical center were included. SLN positive rate, disease-free survival (DFS), and overall survival (OS) were determined. Kaplan-Meier survival, univariate, and multivariate analyses were performed to determine predictive factors for SLN status, DFS, and OS. Results Head and neck melanoma (HNM) had the lowest SLN-positive rate at 10.8 % (16.8 % for extremity and 19.3 % for trunk; P  = 0.002) but had the worst 5-year DFS ( P  < 0.0001) and 5-year OS ( P  < 0.0001) compared with other sites. Tumor thickness ( P  < 0.001), ulceration ( P  < 0.001), HNM location ( P  = 0.001), mitotic rate ( P  < 0.001), and decreasing age ( P  < 0.001) were independent predictive factors for SLN-positivity. HNM with T3 or T4 thickness had significantly lower SLN positive rate compared with other locations ( P  ≤ 0.05). Also, on multivariate analysis, HNM location versus other anatomic sites was independently predictive of decreased DFS and OS ( P  < 0.001). By Kaplan-Meier analysis, HNM was associated significantly with the worst DFS and OS. Conclusions Primary melanoma anatomic location is an independent predictor of SLN status and survival. Although HNM has a decreased SLN-positivity rate, it shows a significantly increased risk of recurrence and death as compared with other sites.]]></description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-013-2977-7</identifier><identifier>PMID: 23649930</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Clinical outcomes ; Extremities - pathology ; Extremities - surgery ; Female ; Follow-Up Studies ; Head and Neck Neoplasms - mortality ; Head and Neck Neoplasms - pathology ; Head and Neck Neoplasms - surgery ; Humans ; Lymphatic Metastasis ; Male ; Medicine ; Medicine &amp; Public Health ; Melanoma - mortality ; Melanoma - pathology ; Melanoma - surgery ; Melanomas ; Middle Aged ; Neoplasm Staging ; Oncology ; Prognosis ; Sentinel Lymph Node Biopsy ; Skin Neoplasms - mortality ; Skin Neoplasms - pathology ; Skin Neoplasms - surgery ; Surgery ; Surgical Oncology ; Survival Rate ; Tertiary Care Centers</subject><ispartof>Annals of surgical oncology, 2013-09, Vol.20 (9), p.3089-3097</ispartof><rights>Society of Surgical Oncology 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-56bd27a44df5224ab3ba9ca363798a5036dd7d67a4f05f693e80e9387b9aa8013</citedby><cites>FETCH-LOGICAL-c372t-56bd27a44df5224ab3ba9ca363798a5036dd7d67a4f05f693e80e9387b9aa8013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1245/s10434-013-2977-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1245/s10434-013-2977-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,41493,42562,51324</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23649930$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fadaki, Niloofar</creatorcontrib><creatorcontrib>Li, Rui</creatorcontrib><creatorcontrib>Parrett, Brian</creatorcontrib><creatorcontrib>Sanders, Grant</creatorcontrib><creatorcontrib>Thummala, Suresh</creatorcontrib><creatorcontrib>Martineau, Lea</creatorcontrib><creatorcontrib>Cardona-Huerta, Servando</creatorcontrib><creatorcontrib>Miranda, Suzette</creatorcontrib><creatorcontrib>Cheng, Shih-Tsung</creatorcontrib><creatorcontrib>Miller, James R.</creatorcontrib><creatorcontrib>Singer, Mark</creatorcontrib><creatorcontrib>Cleaver, James E.</creatorcontrib><creatorcontrib>Kashani-Sabet, Mohammed</creatorcontrib><creatorcontrib>Leong, Stanley P. L.</creatorcontrib><title>Is Head and Neck Melanoma Different from Trunk and Extremity Melanomas with Respect to Sentinel Lymph Node Status and Clinical Outcome?</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><addtitle>Ann Surg Oncol</addtitle><description><![CDATA[Background Previous studies showed conflicting and inconsistent results regarding the effect of anatomic location of the melanoma on sentinel lymph node (SLN) positivity and/or survival. This study was conducted to evaluate and compare the effect of the anatomic locations of primary melanoma on long-term clinical outcomes. Methods All consecutive cutaneous melanoma patients ( n  = 2,079) who underwent selective SLN dissection (SLND) from 1993 to 2009 in a single academic tertiary-care medical center were included. SLN positive rate, disease-free survival (DFS), and overall survival (OS) were determined. Kaplan-Meier survival, univariate, and multivariate analyses were performed to determine predictive factors for SLN status, DFS, and OS. Results Head and neck melanoma (HNM) had the lowest SLN-positive rate at 10.8 % (16.8 % for extremity and 19.3 % for trunk; P  = 0.002) but had the worst 5-year DFS ( P  < 0.0001) and 5-year OS ( P  < 0.0001) compared with other sites. Tumor thickness ( P  < 0.001), ulceration ( P  < 0.001), HNM location ( P  = 0.001), mitotic rate ( P  < 0.001), and decreasing age ( P  < 0.001) were independent predictive factors for SLN-positivity. HNM with T3 or T4 thickness had significantly lower SLN positive rate compared with other locations ( P  ≤ 0.05). Also, on multivariate analysis, HNM location versus other anatomic sites was independently predictive of decreased DFS and OS ( P  < 0.001). By Kaplan-Meier analysis, HNM was associated significantly with the worst DFS and OS. Conclusions Primary melanoma anatomic location is an independent predictor of SLN status and survival. Although HNM has a decreased SLN-positivity rate, it shows a significantly increased risk of recurrence and death as compared with other sites.]]></description><subject>Clinical outcomes</subject><subject>Extremities - pathology</subject><subject>Extremities - surgery</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Head and Neck Neoplasms - mortality</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>Head and Neck Neoplasms - surgery</subject><subject>Humans</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Melanoma - mortality</subject><subject>Melanoma - pathology</subject><subject>Melanoma - surgery</subject><subject>Melanomas</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Prognosis</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Skin Neoplasms - mortality</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - surgery</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Survival Rate</subject><subject>Tertiary Care Centers</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kctO3DAUhi1UxP0BuqksddNNim-x41VVTaEgDSBxWVtOfFICSTzYjtp5Al4bDwOoQmJly-f7_3OOf4Q-U_KdMlEeRkoEFwWhvGBaqUJtoB1a5hchK_op34msCs1kuY12Y7wjhCpOyi20zbgUWnOygx5PIz4B67AdHT6H5h6fQW9HP1j8q2tbCDAm3AY_4OswjffP2NG_FGDo0vKNjfhvl27xJcQFNAknj6-yrhuhx_PlsLjF594Bvko2TfHZYtZ3Y9fYHl9MqfED_NhHm63tIxy8nHvo5vjoenZSzC9-n85-zouGK5aKUtaOKSuEa0vGhK15bXVjueRKV7YkXDqnnMxES8pWag4VAc0rVWtrq_xRe-jb2ncR_MMEMZmhiw30eQ_wUzRU0IoKzhjJ6Nd36J2fwpinW1FKEKorkSm6pprgYwzQmkXoBhuWhhKzSsmsUzK5uVmlZFTWfHlxnuoB3JviNZYMsDUQc2n8A-G_1h-6PgGcGpxz</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Fadaki, Niloofar</creator><creator>Li, Rui</creator><creator>Parrett, Brian</creator><creator>Sanders, Grant</creator><creator>Thummala, Suresh</creator><creator>Martineau, Lea</creator><creator>Cardona-Huerta, Servando</creator><creator>Miranda, Suzette</creator><creator>Cheng, Shih-Tsung</creator><creator>Miller, James R.</creator><creator>Singer, Mark</creator><creator>Cleaver, James E.</creator><creator>Kashani-Sabet, Mohammed</creator><creator>Leong, Stanley P. L.</creator><general>Springer US</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>7X8</scope></search><sort><creationdate>20130901</creationdate><title>Is Head and Neck Melanoma Different from Trunk and Extremity Melanomas with Respect to Sentinel Lymph Node Status and Clinical Outcome?</title><author>Fadaki, Niloofar ; Li, Rui ; Parrett, Brian ; Sanders, Grant ; Thummala, Suresh ; Martineau, Lea ; Cardona-Huerta, Servando ; Miranda, Suzette ; Cheng, Shih-Tsung ; Miller, James R. ; Singer, Mark ; Cleaver, James E. ; Kashani-Sabet, Mohammed ; Leong, Stanley P. 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L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Is Head and Neck Melanoma Different from Trunk and Extremity Melanomas with Respect to Sentinel Lymph Node Status and Clinical Outcome?</atitle><jtitle>Annals of surgical oncology</jtitle><stitle>Ann Surg Oncol</stitle><addtitle>Ann Surg Oncol</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>20</volume><issue>9</issue><spage>3089</spage><epage>3097</epage><pages>3089-3097</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract><![CDATA[Background Previous studies showed conflicting and inconsistent results regarding the effect of anatomic location of the melanoma on sentinel lymph node (SLN) positivity and/or survival. This study was conducted to evaluate and compare the effect of the anatomic locations of primary melanoma on long-term clinical outcomes. Methods All consecutive cutaneous melanoma patients ( n  = 2,079) who underwent selective SLN dissection (SLND) from 1993 to 2009 in a single academic tertiary-care medical center were included. SLN positive rate, disease-free survival (DFS), and overall survival (OS) were determined. Kaplan-Meier survival, univariate, and multivariate analyses were performed to determine predictive factors for SLN status, DFS, and OS. Results Head and neck melanoma (HNM) had the lowest SLN-positive rate at 10.8 % (16.8 % for extremity and 19.3 % for trunk; P  = 0.002) but had the worst 5-year DFS ( P  < 0.0001) and 5-year OS ( P  < 0.0001) compared with other sites. Tumor thickness ( P  < 0.001), ulceration ( P  < 0.001), HNM location ( P  = 0.001), mitotic rate ( P  < 0.001), and decreasing age ( P  < 0.001) were independent predictive factors for SLN-positivity. HNM with T3 or T4 thickness had significantly lower SLN positive rate compared with other locations ( P  ≤ 0.05). Also, on multivariate analysis, HNM location versus other anatomic sites was independently predictive of decreased DFS and OS ( P  < 0.001). By Kaplan-Meier analysis, HNM was associated significantly with the worst DFS and OS. Conclusions Primary melanoma anatomic location is an independent predictor of SLN status and survival. Although HNM has a decreased SLN-positivity rate, it shows a significantly increased risk of recurrence and death as compared with other sites.]]></abstract><cop>Boston</cop><pub>Springer US</pub><pmid>23649930</pmid><doi>10.1245/s10434-013-2977-7</doi><tpages>9</tpages></addata></record>
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subjects Clinical outcomes
Extremities - pathology
Extremities - surgery
Female
Follow-Up Studies
Head and Neck Neoplasms - mortality
Head and Neck Neoplasms - pathology
Head and Neck Neoplasms - surgery
Humans
Lymphatic Metastasis
Male
Medicine
Medicine & Public Health
Melanoma - mortality
Melanoma - pathology
Melanoma - surgery
Melanomas
Middle Aged
Neoplasm Staging
Oncology
Prognosis
Sentinel Lymph Node Biopsy
Skin Neoplasms - mortality
Skin Neoplasms - pathology
Skin Neoplasms - surgery
Surgery
Surgical Oncology
Survival Rate
Tertiary Care Centers
title Is Head and Neck Melanoma Different from Trunk and Extremity Melanomas with Respect to Sentinel Lymph Node Status and Clinical Outcome?
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