Intraoperative sentinel node identification and sampling in clinically node-negative renal cell carcinoma: initial experience in 20 patients
Purpose To apply single-photon emission computed tomography (SPECT) in combination with computed tomography (CT) for preoperative identification of sentinel lymph nodes (SNs) and to investigate surgical feasibility and safety of intraoperative sampling. Methods A retrospective combined interim analy...
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Veröffentlicht in: | World journal of urology 2011-12, Vol.29 (6), p.793-799 |
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creator | Bex, A. Vermeeren, L. Meinhardt, W. Prevoo, W. Horenblas, S. Valdés Olmos, R. A. |
description | Purpose
To apply single-photon emission computed tomography (SPECT) in combination with computed tomography (CT) for preoperative identification of sentinel lymph nodes (SNs) and to investigate surgical feasibility and safety of intraoperative sampling.
Methods
A retrospective combined interim analysis of 20 patients from two prospective trials who underwent injection of 99mTc-nanocolloid into the renal tumour for preoperative identification of SN with SPECT/CT and subsequent removal of the tumour and intraoperative sampling using a gamma probe and portable camera. Lymphadenectomy was completed locoregionally. Surgical approach, time, blood loss, intraoperative yield, Clavien complications and anatomical location of SN in correlation with preoperative imaging were evaluated.
Results
SPECT/CT detected SN in 14/20 patients (70%), including 4 patients with non-visualisation on planar lymphoscintigraphy. Twenty-six SNs were seen: 17 para-aortic (including interaorto-caval), 4 retrocaval, 1 hilar, 1 celiac trunc, 1 internal mammary and 2 mediastinal and pleural. These latter 4 nodes were not harvested according to protocol. All other SNs, except for 2 weakly radioactive interaorto-caval nodes, were identified and excised with a mean additional time of 20 min. None of the removed SN and locoregional nodes was tumour-bearing.
Conclusions
Intraoperative SN identification and sampling in RCC with preoperative detection on SPECT/CT is surgically safe and feasible. SN from the kidney are mainly localised in the para-aortic region, but aberrant nodes receive direct drainage. Non-visualisation of SN appears in almost a third of the patients. Further studies are required to demonstrate whether accurate mapping of lymphatic drainage and extent of lymphatic spread may have diagnostic and therapeutic implications. |
doi_str_mv | 10.1007/s00345-010-0615-6 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_906152983</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2518844771</sourcerecordid><originalsourceid>FETCH-LOGICAL-c370t-6ad52dba19b98e87818b85753223069bce9ae9a123650db1819c749429b94d053</originalsourceid><addsrcrecordid>eNp1kc1u1TAQhS0EorctD8AGRWxYGcaOHTvsUAW0UqVu6NpynLlXrhIn2LmIvkMfmgkpICFVsvw33zljzzD2WsB7AWA-FIBaaQ4CODRC8-YZ2wlV19wa2TxnOzBScdXa-oSdlnIHIEwD-iU7kUKAsUrv2MNVWrKfZsx-iT-wKpiWmHCo0tRjFfv1uI-BglOqfOqr4sd5iOlQxVQF2lBsGO5_4zzhYXPJmPxQBRxo8jnENI3-IyniEukef1K6iCngaiKhmklFico5e7H3Q8FXj-sZu_3y-dvFJb---Xp18emah9rAwhvfa9l3XrRda9EaK2xntdG1lDU0bRew9TSErBsNfSesaINRrZLEqx50fcbebb5znr4fsSxujGV9rU84HYtr12pKqhuRb_8j76Zjps-tkLZWKmkJEhsU8lRKxr2bcxx9vncC3NootzXKUaPcau0a0rx5ND52I_Z_FX86Q4DcgEKhdMD8L_PTrr8AviKfCg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>905882428</pqid></control><display><type>article</type><title>Intraoperative sentinel node identification and sampling in clinically node-negative renal cell carcinoma: initial experience in 20 patients</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Bex, A. ; Vermeeren, L. ; Meinhardt, W. ; Prevoo, W. ; Horenblas, S. ; Valdés Olmos, R. A.</creator><creatorcontrib>Bex, A. ; Vermeeren, L. ; Meinhardt, W. ; Prevoo, W. ; Horenblas, S. ; Valdés Olmos, R. A.</creatorcontrib><description>Purpose
To apply single-photon emission computed tomography (SPECT) in combination with computed tomography (CT) for preoperative identification of sentinel lymph nodes (SNs) and to investigate surgical feasibility and safety of intraoperative sampling.
Methods
A retrospective combined interim analysis of 20 patients from two prospective trials who underwent injection of 99mTc-nanocolloid into the renal tumour for preoperative identification of SN with SPECT/CT and subsequent removal of the tumour and intraoperative sampling using a gamma probe and portable camera. Lymphadenectomy was completed locoregionally. Surgical approach, time, blood loss, intraoperative yield, Clavien complications and anatomical location of SN in correlation with preoperative imaging were evaluated.
Results
SPECT/CT detected SN in 14/20 patients (70%), including 4 patients with non-visualisation on planar lymphoscintigraphy. Twenty-six SNs were seen: 17 para-aortic (including interaorto-caval), 4 retrocaval, 1 hilar, 1 celiac trunc, 1 internal mammary and 2 mediastinal and pleural. These latter 4 nodes were not harvested according to protocol. All other SNs, except for 2 weakly radioactive interaorto-caval nodes, were identified and excised with a mean additional time of 20 min. None of the removed SN and locoregional nodes was tumour-bearing.
Conclusions
Intraoperative SN identification and sampling in RCC with preoperative detection on SPECT/CT is surgically safe and feasible. SN from the kidney are mainly localised in the para-aortic region, but aberrant nodes receive direct drainage. Non-visualisation of SN appears in almost a third of the patients. Further studies are required to demonstrate whether accurate mapping of lymphatic drainage and extent of lymphatic spread may have diagnostic and therapeutic implications.</description><identifier>ISSN: 0724-4983</identifier><identifier>EISSN: 1433-8726</identifier><identifier>DOI: 10.1007/s00345-010-0615-6</identifier><identifier>PMID: 21107845</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Adult ; Aged ; Blood Loss, Surgical ; Carcinoma, Renal Cell - diagnostic imaging ; Carcinoma, Renal Cell - surgery ; Female ; Humans ; Intraoperative Period ; Kidney - diagnostic imaging ; Kidney - surgery ; Kidney Neoplasms - diagnostic imaging ; Kidney Neoplasms - surgery ; Lymph Nodes - diagnostic imaging ; Lymph Nodes - surgery ; Lymphatic Metastasis - diagnostic imaging ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Multimodal Imaging - adverse effects ; Nephrology ; Oncology ; Original Article ; Positron-Emission Tomography ; Retrospective Studies ; Sentinel Lymph Node Biopsy - methods ; Technetium ; Time Factors ; Tomography, X-Ray Computed ; Urology</subject><ispartof>World journal of urology, 2011-12, Vol.29 (6), p.793-799</ispartof><rights>Springer-Verlag 2010</rights><rights>Springer-Verlag 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-6ad52dba19b98e87818b85753223069bce9ae9a123650db1819c749429b94d053</citedby><cites>FETCH-LOGICAL-c370t-6ad52dba19b98e87818b85753223069bce9ae9a123650db1819c749429b94d053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00345-010-0615-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00345-010-0615-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21107845$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bex, A.</creatorcontrib><creatorcontrib>Vermeeren, L.</creatorcontrib><creatorcontrib>Meinhardt, W.</creatorcontrib><creatorcontrib>Prevoo, W.</creatorcontrib><creatorcontrib>Horenblas, S.</creatorcontrib><creatorcontrib>Valdés Olmos, R. A.</creatorcontrib><title>Intraoperative sentinel node identification and sampling in clinically node-negative renal cell carcinoma: initial experience in 20 patients</title><title>World journal of urology</title><addtitle>World J Urol</addtitle><addtitle>World J Urol</addtitle><description>Purpose
To apply single-photon emission computed tomography (SPECT) in combination with computed tomography (CT) for preoperative identification of sentinel lymph nodes (SNs) and to investigate surgical feasibility and safety of intraoperative sampling.
Methods
A retrospective combined interim analysis of 20 patients from two prospective trials who underwent injection of 99mTc-nanocolloid into the renal tumour for preoperative identification of SN with SPECT/CT and subsequent removal of the tumour and intraoperative sampling using a gamma probe and portable camera. Lymphadenectomy was completed locoregionally. Surgical approach, time, blood loss, intraoperative yield, Clavien complications and anatomical location of SN in correlation with preoperative imaging were evaluated.
Results
SPECT/CT detected SN in 14/20 patients (70%), including 4 patients with non-visualisation on planar lymphoscintigraphy. Twenty-six SNs were seen: 17 para-aortic (including interaorto-caval), 4 retrocaval, 1 hilar, 1 celiac trunc, 1 internal mammary and 2 mediastinal and pleural. These latter 4 nodes were not harvested according to protocol. All other SNs, except for 2 weakly radioactive interaorto-caval nodes, were identified and excised with a mean additional time of 20 min. None of the removed SN and locoregional nodes was tumour-bearing.
Conclusions
Intraoperative SN identification and sampling in RCC with preoperative detection on SPECT/CT is surgically safe and feasible. SN from the kidney are mainly localised in the para-aortic region, but aberrant nodes receive direct drainage. Non-visualisation of SN appears in almost a third of the patients. Further studies are required to demonstrate whether accurate mapping of lymphatic drainage and extent of lymphatic spread may have diagnostic and therapeutic implications.</description><subject>Adult</subject><subject>Aged</subject><subject>Blood Loss, Surgical</subject><subject>Carcinoma, Renal Cell - diagnostic imaging</subject><subject>Carcinoma, Renal Cell - surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Intraoperative Period</subject><subject>Kidney - diagnostic imaging</subject><subject>Kidney - surgery</subject><subject>Kidney Neoplasms - diagnostic imaging</subject><subject>Kidney Neoplasms - surgery</subject><subject>Lymph Nodes - diagnostic imaging</subject><subject>Lymph Nodes - surgery</subject><subject>Lymphatic Metastasis - diagnostic imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Multimodal Imaging - adverse effects</subject><subject>Nephrology</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Positron-Emission Tomography</subject><subject>Retrospective Studies</subject><subject>Sentinel Lymph Node Biopsy - methods</subject><subject>Technetium</subject><subject>Time Factors</subject><subject>Tomography, X-Ray Computed</subject><subject>Urology</subject><issn>0724-4983</issn><issn>1433-8726</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kc1u1TAQhS0EorctD8AGRWxYGcaOHTvsUAW0UqVu6NpynLlXrhIn2LmIvkMfmgkpICFVsvw33zljzzD2WsB7AWA-FIBaaQ4CODRC8-YZ2wlV19wa2TxnOzBScdXa-oSdlnIHIEwD-iU7kUKAsUrv2MNVWrKfZsx-iT-wKpiWmHCo0tRjFfv1uI-BglOqfOqr4sd5iOlQxVQF2lBsGO5_4zzhYXPJmPxQBRxo8jnENI3-IyniEukef1K6iCngaiKhmklFico5e7H3Q8FXj-sZu_3y-dvFJb---Xp18emah9rAwhvfa9l3XrRda9EaK2xntdG1lDU0bRew9TSErBsNfSesaINRrZLEqx50fcbebb5znr4fsSxujGV9rU84HYtr12pKqhuRb_8j76Zjps-tkLZWKmkJEhsU8lRKxr2bcxx9vncC3NootzXKUaPcau0a0rx5ND52I_Z_FX86Q4DcgEKhdMD8L_PTrr8AviKfCg</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Bex, A.</creator><creator>Vermeeren, L.</creator><creator>Meinhardt, W.</creator><creator>Prevoo, W.</creator><creator>Horenblas, S.</creator><creator>Valdés Olmos, R. A.</creator><general>Springer-Verlag</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>7T5</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>20111201</creationdate><title>Intraoperative sentinel node identification and sampling in clinically node-negative renal cell carcinoma: initial experience in 20 patients</title><author>Bex, A. ; Vermeeren, L. ; Meinhardt, W. ; Prevoo, W. ; Horenblas, S. ; Valdés Olmos, R. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-6ad52dba19b98e87818b85753223069bce9ae9a123650db1819c749429b94d053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Blood Loss, Surgical</topic><topic>Carcinoma, Renal Cell - diagnostic imaging</topic><topic>Carcinoma, Renal Cell - surgery</topic><topic>Female</topic><topic>Humans</topic><topic>Intraoperative Period</topic><topic>Kidney - diagnostic imaging</topic><topic>Kidney - surgery</topic><topic>Kidney Neoplasms - diagnostic imaging</topic><topic>Kidney Neoplasms - surgery</topic><topic>Lymph Nodes - diagnostic imaging</topic><topic>Lymph Nodes - surgery</topic><topic>Lymphatic Metastasis - diagnostic imaging</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Multimodal Imaging - adverse effects</topic><topic>Nephrology</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Positron-Emission Tomography</topic><topic>Retrospective Studies</topic><topic>Sentinel Lymph Node Biopsy - methods</topic><topic>Technetium</topic><topic>Time Factors</topic><topic>Tomography, X-Ray Computed</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bex, A.</creatorcontrib><creatorcontrib>Vermeeren, L.</creatorcontrib><creatorcontrib>Meinhardt, W.</creatorcontrib><creatorcontrib>Prevoo, W.</creatorcontrib><creatorcontrib>Horenblas, S.</creatorcontrib><creatorcontrib>Valdés Olmos, R. A.</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>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>World journal of urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bex, A.</au><au>Vermeeren, L.</au><au>Meinhardt, W.</au><au>Prevoo, W.</au><au>Horenblas, S.</au><au>Valdés Olmos, R. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraoperative sentinel node identification and sampling in clinically node-negative renal cell carcinoma: initial experience in 20 patients</atitle><jtitle>World journal of urology</jtitle><stitle>World J Urol</stitle><addtitle>World J Urol</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>29</volume><issue>6</issue><spage>793</spage><epage>799</epage><pages>793-799</pages><issn>0724-4983</issn><eissn>1433-8726</eissn><abstract>Purpose
To apply single-photon emission computed tomography (SPECT) in combination with computed tomography (CT) for preoperative identification of sentinel lymph nodes (SNs) and to investigate surgical feasibility and safety of intraoperative sampling.
Methods
A retrospective combined interim analysis of 20 patients from two prospective trials who underwent injection of 99mTc-nanocolloid into the renal tumour for preoperative identification of SN with SPECT/CT and subsequent removal of the tumour and intraoperative sampling using a gamma probe and portable camera. Lymphadenectomy was completed locoregionally. Surgical approach, time, blood loss, intraoperative yield, Clavien complications and anatomical location of SN in correlation with preoperative imaging were evaluated.
Results
SPECT/CT detected SN in 14/20 patients (70%), including 4 patients with non-visualisation on planar lymphoscintigraphy. Twenty-six SNs were seen: 17 para-aortic (including interaorto-caval), 4 retrocaval, 1 hilar, 1 celiac trunc, 1 internal mammary and 2 mediastinal and pleural. These latter 4 nodes were not harvested according to protocol. All other SNs, except for 2 weakly radioactive interaorto-caval nodes, were identified and excised with a mean additional time of 20 min. None of the removed SN and locoregional nodes was tumour-bearing.
Conclusions
Intraoperative SN identification and sampling in RCC with preoperative detection on SPECT/CT is surgically safe and feasible. SN from the kidney are mainly localised in the para-aortic region, but aberrant nodes receive direct drainage. Non-visualisation of SN appears in almost a third of the patients. Further studies are required to demonstrate whether accurate mapping of lymphatic drainage and extent of lymphatic spread may have diagnostic and therapeutic implications.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21107845</pmid><doi>10.1007/s00345-010-0615-6</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Blood Loss, Surgical Carcinoma, Renal Cell - diagnostic imaging Carcinoma, Renal Cell - surgery Female Humans Intraoperative Period Kidney - diagnostic imaging Kidney - surgery Kidney Neoplasms - diagnostic imaging Kidney Neoplasms - surgery Lymph Nodes - diagnostic imaging Lymph Nodes - surgery Lymphatic Metastasis - diagnostic imaging Male Medicine Medicine & Public Health Middle Aged Multimodal Imaging - adverse effects Nephrology Oncology Original Article Positron-Emission Tomography Retrospective Studies Sentinel Lymph Node Biopsy - methods Technetium Time Factors Tomography, X-Ray Computed Urology |
title | Intraoperative sentinel node identification and sampling in clinically node-negative renal cell carcinoma: initial experience in 20 patients |
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