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Regional control after precision lymph node dissection for clinically evident melanoma metastasis
Introduction Completion lymph node dissection (CLND) for microscopic lymph node metastases has been replaced by observation; however, CLND is standard for clinically detectable nodal metastases (cLN). CLND has high morbidity, which may be reduced by excision of only the cLN (precision lymph node dis...
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Published in: | Journal of surgical oncology 2023-01, Vol.127 (1), p.140-147 |
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creator | Lynch, Kevin T. Hu, Yinin Farrow, Norma E. Song, Yun Meneveau, Max O. Kwak, Minyoung Lowe, Michael C. Bartlett, Edmund K. Beasley, Georgia M. Karakousis, Giorgos C. Slingluff, Craig L. |
description | Introduction
Completion lymph node dissection (CLND) for microscopic lymph node metastases has been replaced by observation; however, CLND is standard for clinically detectable nodal metastases (cLN). CLND has high morbidity, which may be reduced by excision of only the cLN (precision lymph node dissection [PLND]). We hypothesized that same‐basin recurrence risk would be low after PLND.
Methods
Retrospective review at four tertiary care hospitals identified patients who underwent PLND. The primary outcome was 3‐year cumulative incidence of isolated same‐basin recurrence.
Results
Twenty‐one patients underwent PLND for cLN without synchronous distant metastases. Reasons for forgoing CLND included patient preference (n = 11), comorbidities (n = 5), imaging indeterminate for distant metastases (n = 2), partial response to checkpoint blockade (n = 1), or not reported (n = 2). A median of 2 nodes (range: 1–6) were resected at PLND, and 68% contained melanoma. Recurrence was observed in 33% overall. Only 1 patient (5%) developed an isolated same‐basin recurrence. Cumulative incidences at 3 years were 5.0%, 17.3%, and 49.7% for isolated same‐basin recurrence, any same‐basin recurrence, and any recurrence, respectively. Complications from PLND were reported in 1 patient (5%).
Conclusions
These pilot data suggest that PLND may provide adequate regional disease control with less morbidity than CLND. These data justify prospective evaluation of PLND in select patients. |
doi_str_mv | 10.1002/jso.27100 |
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Completion lymph node dissection (CLND) for microscopic lymph node metastases has been replaced by observation; however, CLND is standard for clinically detectable nodal metastases (cLN). CLND has high morbidity, which may be reduced by excision of only the cLN (precision lymph node dissection [PLND]). We hypothesized that same‐basin recurrence risk would be low after PLND.
Methods
Retrospective review at four tertiary care hospitals identified patients who underwent PLND. The primary outcome was 3‐year cumulative incidence of isolated same‐basin recurrence.
Results
Twenty‐one patients underwent PLND for cLN without synchronous distant metastases. Reasons for forgoing CLND included patient preference (n = 11), comorbidities (n = 5), imaging indeterminate for distant metastases (n = 2), partial response to checkpoint blockade (n = 1), or not reported (n = 2). A median of 2 nodes (range: 1–6) were resected at PLND, and 68% contained melanoma. Recurrence was observed in 33% overall. Only 1 patient (5%) developed an isolated same‐basin recurrence. Cumulative incidences at 3 years were 5.0%, 17.3%, and 49.7% for isolated same‐basin recurrence, any same‐basin recurrence, and any recurrence, respectively. Complications from PLND were reported in 1 patient (5%).
Conclusions
These pilot data suggest that PLND may provide adequate regional disease control with less morbidity than CLND. These data justify prospective evaluation of PLND in select patients.</description><identifier>ISSN: 0022-4790</identifier><identifier>ISSN: 1096-9098</identifier><identifier>EISSN: 1096-9098</identifier><identifier>DOI: 10.1002/jso.27100</identifier><identifier>PMID: 36115028</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Dissection ; Humans ; Lymph Node Excision ; Lymph Nodes - pathology ; Lymphatic Metastasis - pathology ; Lymphatic system ; Melanoma ; Melanoma - pathology ; Metastasis ; nodal metastases ; Patients ; precision nodal dissection ; Retrospective Studies ; Sentinel Lymph Node Biopsy ; Skin Neoplasms - pathology ; Skin Neoplasms - surgery ; Syndrome</subject><ispartof>Journal of surgical oncology, 2023-01, Vol.127 (1), p.140-147</ispartof><rights>2022 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3530-88b1fd1880f8a8dca81d84990743f5eb5bc679039e00672b32d852adc55c2a8c3</citedby><cites>FETCH-LOGICAL-c3530-88b1fd1880f8a8dca81d84990743f5eb5bc679039e00672b32d852adc55c2a8c3</cites><orcidid>0000-0002-9845-6617 ; 0000-0002-0923-153X ; 0000-0002-0404-214X ; 0000-0003-4853-7352 ; 0000-0001-6387-9030</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36115028$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lynch, Kevin T.</creatorcontrib><creatorcontrib>Hu, Yinin</creatorcontrib><creatorcontrib>Farrow, Norma E.</creatorcontrib><creatorcontrib>Song, Yun</creatorcontrib><creatorcontrib>Meneveau, Max O.</creatorcontrib><creatorcontrib>Kwak, Minyoung</creatorcontrib><creatorcontrib>Lowe, Michael C.</creatorcontrib><creatorcontrib>Bartlett, Edmund K.</creatorcontrib><creatorcontrib>Beasley, Georgia M.</creatorcontrib><creatorcontrib>Karakousis, Giorgos C.</creatorcontrib><creatorcontrib>Slingluff, Craig L.</creatorcontrib><title>Regional control after precision lymph node dissection for clinically evident melanoma metastasis</title><title>Journal of surgical oncology</title><addtitle>J Surg Oncol</addtitle><description>Introduction
Completion lymph node dissection (CLND) for microscopic lymph node metastases has been replaced by observation; however, CLND is standard for clinically detectable nodal metastases (cLN). CLND has high morbidity, which may be reduced by excision of only the cLN (precision lymph node dissection [PLND]). We hypothesized that same‐basin recurrence risk would be low after PLND.
Methods
Retrospective review at four tertiary care hospitals identified patients who underwent PLND. The primary outcome was 3‐year cumulative incidence of isolated same‐basin recurrence.
Results
Twenty‐one patients underwent PLND for cLN without synchronous distant metastases. Reasons for forgoing CLND included patient preference (n = 11), comorbidities (n = 5), imaging indeterminate for distant metastases (n = 2), partial response to checkpoint blockade (n = 1), or not reported (n = 2). A median of 2 nodes (range: 1–6) were resected at PLND, and 68% contained melanoma. Recurrence was observed in 33% overall. Only 1 patient (5%) developed an isolated same‐basin recurrence. Cumulative incidences at 3 years were 5.0%, 17.3%, and 49.7% for isolated same‐basin recurrence, any same‐basin recurrence, and any recurrence, respectively. Complications from PLND were reported in 1 patient (5%).
Conclusions
These pilot data suggest that PLND may provide adequate regional disease control with less morbidity than CLND. These data justify prospective evaluation of PLND in select patients.</description><subject>Dissection</subject><subject>Humans</subject><subject>Lymph Node Excision</subject><subject>Lymph Nodes - pathology</subject><subject>Lymphatic Metastasis - pathology</subject><subject>Lymphatic system</subject><subject>Melanoma</subject><subject>Melanoma - pathology</subject><subject>Metastasis</subject><subject>nodal metastases</subject><subject>Patients</subject><subject>precision nodal dissection</subject><subject>Retrospective Studies</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - surgery</subject><subject>Syndrome</subject><issn>0022-4790</issn><issn>1096-9098</issn><issn>1096-9098</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kMtqHDEQRYVJsMePhX_ACLKJF22XXj3SMpg8MRhsZ92opepEg7o1kXpi5u-jyTheGAIFVagOl9Ih5JzBFQPg16uSrviyjgdkwcC0jQGj35BF3fFGLg0ckeNSVgBgTCsPyZFoGVPA9YLYe_wR0mQjdWmac4rUDjNmus7oQqkbGrfj-iedkkfqQyno5t3rkDJ1MUzB2Ri3FH8Hj9NMR4x2SqOtw2xLrVBOydvBxoJnz_2EfP_08fHmS3N79_nrzYfbxgkloNG6Z4NnWsOgrfbOaua1NAaWUgwKe9W7tv5EGARol7wX3GvFrXdKOW61Eyfk_T53ndOvDZa5G0NxGOtBmDalq4KUlK1QbUXfvUJXaZOrhB0lWymBCV6pyz3lciol49Ctcxht3nYMup33rnrv_nqv7MVz4qYf0b-Q_0RX4HoPPIWI2_8ndd8e7vaRfwCobYzZ</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Lynch, Kevin T.</creator><creator>Hu, Yinin</creator><creator>Farrow, Norma E.</creator><creator>Song, Yun</creator><creator>Meneveau, Max O.</creator><creator>Kwak, Minyoung</creator><creator>Lowe, Michael C.</creator><creator>Bartlett, Edmund K.</creator><creator>Beasley, Georgia M.</creator><creator>Karakousis, Giorgos C.</creator><creator>Slingluff, Craig L.</creator><general>Wiley Subscription Services, Inc</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>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9845-6617</orcidid><orcidid>https://orcid.org/0000-0002-0923-153X</orcidid><orcidid>https://orcid.org/0000-0002-0404-214X</orcidid><orcidid>https://orcid.org/0000-0003-4853-7352</orcidid><orcidid>https://orcid.org/0000-0001-6387-9030</orcidid></search><sort><creationdate>202301</creationdate><title>Regional control after precision lymph node dissection for clinically evident melanoma metastasis</title><author>Lynch, Kevin T. ; Hu, Yinin ; Farrow, Norma E. ; Song, Yun ; Meneveau, Max O. ; Kwak, Minyoung ; Lowe, Michael C. ; Bartlett, Edmund K. ; Beasley, Georgia M. ; Karakousis, Giorgos C. ; Slingluff, Craig L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3530-88b1fd1880f8a8dca81d84990743f5eb5bc679039e00672b32d852adc55c2a8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Dissection</topic><topic>Humans</topic><topic>Lymph Node Excision</topic><topic>Lymph Nodes - pathology</topic><topic>Lymphatic Metastasis - pathology</topic><topic>Lymphatic system</topic><topic>Melanoma</topic><topic>Melanoma - pathology</topic><topic>Metastasis</topic><topic>nodal metastases</topic><topic>Patients</topic><topic>precision nodal dissection</topic><topic>Retrospective Studies</topic><topic>Sentinel Lymph Node Biopsy</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - surgery</topic><topic>Syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lynch, Kevin T.</creatorcontrib><creatorcontrib>Hu, Yinin</creatorcontrib><creatorcontrib>Farrow, Norma E.</creatorcontrib><creatorcontrib>Song, Yun</creatorcontrib><creatorcontrib>Meneveau, Max O.</creatorcontrib><creatorcontrib>Kwak, Minyoung</creatorcontrib><creatorcontrib>Lowe, Michael C.</creatorcontrib><creatorcontrib>Bartlett, Edmund K.</creatorcontrib><creatorcontrib>Beasley, Georgia M.</creatorcontrib><creatorcontrib>Karakousis, Giorgos C.</creatorcontrib><creatorcontrib>Slingluff, Craig L.</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 Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynch, Kevin T.</au><au>Hu, Yinin</au><au>Farrow, Norma E.</au><au>Song, Yun</au><au>Meneveau, Max O.</au><au>Kwak, Minyoung</au><au>Lowe, Michael C.</au><au>Bartlett, Edmund K.</au><au>Beasley, Georgia M.</au><au>Karakousis, Giorgos C.</au><au>Slingluff, Craig L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regional control after precision lymph node dissection for clinically evident melanoma metastasis</atitle><jtitle>Journal of surgical oncology</jtitle><addtitle>J Surg Oncol</addtitle><date>2023-01</date><risdate>2023</risdate><volume>127</volume><issue>1</issue><spage>140</spage><epage>147</epage><pages>140-147</pages><issn>0022-4790</issn><issn>1096-9098</issn><eissn>1096-9098</eissn><abstract>Introduction
Completion lymph node dissection (CLND) for microscopic lymph node metastases has been replaced by observation; however, CLND is standard for clinically detectable nodal metastases (cLN). CLND has high morbidity, which may be reduced by excision of only the cLN (precision lymph node dissection [PLND]). We hypothesized that same‐basin recurrence risk would be low after PLND.
Methods
Retrospective review at four tertiary care hospitals identified patients who underwent PLND. The primary outcome was 3‐year cumulative incidence of isolated same‐basin recurrence.
Results
Twenty‐one patients underwent PLND for cLN without synchronous distant metastases. Reasons for forgoing CLND included patient preference (n = 11), comorbidities (n = 5), imaging indeterminate for distant metastases (n = 2), partial response to checkpoint blockade (n = 1), or not reported (n = 2). A median of 2 nodes (range: 1–6) were resected at PLND, and 68% contained melanoma. Recurrence was observed in 33% overall. Only 1 patient (5%) developed an isolated same‐basin recurrence. Cumulative incidences at 3 years were 5.0%, 17.3%, and 49.7% for isolated same‐basin recurrence, any same‐basin recurrence, and any recurrence, respectively. Complications from PLND were reported in 1 patient (5%).
Conclusions
These pilot data suggest that PLND may provide adequate regional disease control with less morbidity than CLND. These data justify prospective evaluation of PLND in select patients.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36115028</pmid><doi>10.1002/jso.27100</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-9845-6617</orcidid><orcidid>https://orcid.org/0000-0002-0923-153X</orcidid><orcidid>https://orcid.org/0000-0002-0404-214X</orcidid><orcidid>https://orcid.org/0000-0003-4853-7352</orcidid><orcidid>https://orcid.org/0000-0001-6387-9030</orcidid></addata></record> |
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subjects | Dissection Humans Lymph Node Excision Lymph Nodes - pathology Lymphatic Metastasis - pathology Lymphatic system Melanoma Melanoma - pathology Metastasis nodal metastases Patients precision nodal dissection Retrospective Studies Sentinel Lymph Node Biopsy Skin Neoplasms - pathology Skin Neoplasms - surgery Syndrome |
title | Regional control after precision lymph node dissection for clinically evident melanoma metastasis |
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