Criteria for evaluation of disease extent by 123I-metaiodobenzylguanidine scans in neuroblastoma: a report for the International Neuroblastoma Risk Group (INRG) Task Force
Background: Neuroblastoma is an embryonic tumour of the sympathetic nervous system, metastatic in half of the patients at diagnosis, with a high preponderance of osteomedullary disease, making accurate evaluation of metastatic sites and response to therapy challenging. Metaiodobenzylguanidine (mIBG)...
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creator | Matthay, K K Shulkin, B Ladenstein, R Michon, J Giammarile, F Lewington, V Pearson, A D J Cohn, S L |
description | Background:
Neuroblastoma is an embryonic tumour of the sympathetic nervous system, metastatic in half of the patients at diagnosis, with a high preponderance of osteomedullary disease, making accurate evaluation of metastatic sites and response to therapy challenging. Metaiodobenzylguanidine (mIBG), taken into cells via the norepinephrine transporter, provides a sensitive and specific method of assessing tumour in both soft tissue and bone sites. The goal of this report was to develop consensus guidelines for the use of mIBG scans in staging, response assessment and surveillance in neuroblastoma.
Methods:
The International Neuroblastoma Risk Group (INRG) Task Force, including a multidisciplinary group in paediatric oncology of North and South America, Europe, Oceania and Asia, formed a subcommittee on metastatic disease evaluation, including expert nuclear medicine physicians and oncologists, who developed these guidelines based on their experience and the medical literature, with approval by the larger INRG Task Force.
Results:
Guidelines for patient preparation, radiotracer administration, techniques of scanning including timing, energy, specific views, and use of single photon emission computed tomography are included. Optimal timing of scans in relation to therapy and for surveillance is reviewed. Validated semi-quantitative scoring methods in current use are reviewed, with recommendations for use in prognosis and response evaluation.
Conclusions:
Metaiodobenzylguanidine scans are the most sensitive and specific method of staging and response evaluation in neuroblastoma, particularly when used with a semi-quantitative scoring method. Use of the optimal techniques for mIBG in staging and response, including a semi-quantitative score, is essential for evaluation of the efficacy of new therapy. |
doi_str_mv | 10.1038/sj.bjc.6605621 |
format | Article |
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Neuroblastoma is an embryonic tumour of the sympathetic nervous system, metastatic in half of the patients at diagnosis, with a high preponderance of osteomedullary disease, making accurate evaluation of metastatic sites and response to therapy challenging. Metaiodobenzylguanidine (mIBG), taken into cells via the norepinephrine transporter, provides a sensitive and specific method of assessing tumour in both soft tissue and bone sites. The goal of this report was to develop consensus guidelines for the use of mIBG scans in staging, response assessment and surveillance in neuroblastoma.
Methods:
The International Neuroblastoma Risk Group (INRG) Task Force, including a multidisciplinary group in paediatric oncology of North and South America, Europe, Oceania and Asia, formed a subcommittee on metastatic disease evaluation, including expert nuclear medicine physicians and oncologists, who developed these guidelines based on their experience and the medical literature, with approval by the larger INRG Task Force.
Results:
Guidelines for patient preparation, radiotracer administration, techniques of scanning including timing, energy, specific views, and use of single photon emission computed tomography are included. Optimal timing of scans in relation to therapy and for surveillance is reviewed. Validated semi-quantitative scoring methods in current use are reviewed, with recommendations for use in prognosis and response evaluation.
Conclusions:
Metaiodobenzylguanidine scans are the most sensitive and specific method of staging and response evaluation in neuroblastoma, particularly when used with a semi-quantitative scoring method. Use of the optimal techniques for mIBG in staging and response, including a semi-quantitative score, is essential for evaluation of the efficacy of new therapy.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/sj.bjc.6605621</identifier><identifier>PMID: 20424613</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/378/1689/1690 ; 692/700/139/1677 ; 692/700/1421/1771 ; 692/700/1538 ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Bone marrow ; Cancer Research ; Cancer therapies ; Drug Resistance ; Epidemiology ; full-paper ; Guidelines ; Medical prognosis ; Medical research ; Medical sciences ; Metastasis ; Molecular Medicine ; Nervous system ; Neuroblastoma ; Neurology ; Nuclear medicine ; Oncology ; Pediatrics ; Surveillance ; Task forces ; Tumors ; Tumors of the nervous system. Phacomatoses</subject><ispartof>British journal of cancer, 2010-04, Vol.102 (9), p.1319-1326</ispartof><rights>The Author(s) 2010</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Apr 27, 2010</rights><rights>Copyright © 2010 Cancer Research UK 2010 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3421-326ec0c2555f9717fab5f68795fc9eeed19b37c549f457e8b584aaa62977b64c3</citedby><cites>FETCH-LOGICAL-c3421-326ec0c2555f9717fab5f68795fc9eeed19b37c549f457e8b584aaa62977b64c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2865749/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2865749/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23000277$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Matthay, K K</creatorcontrib><creatorcontrib>Shulkin, B</creatorcontrib><creatorcontrib>Ladenstein, R</creatorcontrib><creatorcontrib>Michon, J</creatorcontrib><creatorcontrib>Giammarile, F</creatorcontrib><creatorcontrib>Lewington, V</creatorcontrib><creatorcontrib>Pearson, A D J</creatorcontrib><creatorcontrib>Cohn, S L</creatorcontrib><title>Criteria for evaluation of disease extent by 123I-metaiodobenzylguanidine scans in neuroblastoma: a report for the International Neuroblastoma Risk Group (INRG) Task Force</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><description>Background:
Neuroblastoma is an embryonic tumour of the sympathetic nervous system, metastatic in half of the patients at diagnosis, with a high preponderance of osteomedullary disease, making accurate evaluation of metastatic sites and response to therapy challenging. Metaiodobenzylguanidine (mIBG), taken into cells via the norepinephrine transporter, provides a sensitive and specific method of assessing tumour in both soft tissue and bone sites. The goal of this report was to develop consensus guidelines for the use of mIBG scans in staging, response assessment and surveillance in neuroblastoma.
Methods:
The International Neuroblastoma Risk Group (INRG) Task Force, including a multidisciplinary group in paediatric oncology of North and South America, Europe, Oceania and Asia, formed a subcommittee on metastatic disease evaluation, including expert nuclear medicine physicians and oncologists, who developed these guidelines based on their experience and the medical literature, with approval by the larger INRG Task Force.
Results:
Guidelines for patient preparation, radiotracer administration, techniques of scanning including timing, energy, specific views, and use of single photon emission computed tomography are included. Optimal timing of scans in relation to therapy and for surveillance is reviewed. Validated semi-quantitative scoring methods in current use are reviewed, with recommendations for use in prognosis and response evaluation.
Conclusions:
Metaiodobenzylguanidine scans are the most sensitive and specific method of staging and response evaluation in neuroblastoma, particularly when used with a semi-quantitative scoring method. Use of the optimal techniques for mIBG in staging and response, including a semi-quantitative score, is essential for evaluation of the efficacy of new therapy.</description><subject>631/378/1689/1690</subject><subject>692/700/139/1677</subject><subject>692/700/1421/1771</subject><subject>692/700/1538</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bone marrow</subject><subject>Cancer Research</subject><subject>Cancer therapies</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>full-paper</subject><subject>Guidelines</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Metastasis</subject><subject>Molecular Medicine</subject><subject>Nervous system</subject><subject>Neuroblastoma</subject><subject>Neurology</subject><subject>Nuclear medicine</subject><subject>Oncology</subject><subject>Pediatrics</subject><subject>Surveillance</subject><subject>Task forces</subject><subject>Tumors</subject><subject>Tumors of the nervous system. Phacomatoses</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkV9rFDEUxQdR7Lb66nMQBPsw2_yZTCY-CLLYdaFUKPU53Mne2WacTdZkprh-Jb-ksbuUCj5dcu_vnsPNKYo3jM4ZFc1F6udtb-d1TWXN2bNixqTgJWu4el7MKKWqpJrTk-I0pT4_NW3Uy-KE04pXNROz4vciuhGjA9KFSPAehglGFzwJHVm7hJCQ4M8R_UjaPWFcrMotjuDCOrTof-2HzQTerZ1Hkiz4RJwnHqcY2gHSGLbwgQCJuAtxfHAY75CsfHb0DzYwkOunNLlx6TtZxjDtyPvV9c3ynNxC7lyGaPFV8aKDIeHrYz0rvl1-vl18Ka--LleLT1elFRVnpeA1Wmq5lLLTiqkOWtnVjdKysxoR10y3QllZ6a6SCptWNhUA1Fwr1daVFWfFx4Pubmq3uLb5-AiD2UW3hbg3AZz5d-LdndmEe8ObWqpKZ4G3R4EYfkyYRtOHKV88JMO0aCqla5mh-QGyMaQUsXs0YNT8zdak3uRszTHbvPDuqAr5q4cugrcuPW5xkfPlSmXu4sClPPIbjE_c_6_8Bzt0twc</recordid><startdate>20100427</startdate><enddate>20100427</enddate><creator>Matthay, K K</creator><creator>Shulkin, B</creator><creator>Ladenstein, R</creator><creator>Michon, J</creator><creator>Giammarile, F</creator><creator>Lewington, V</creator><creator>Pearson, A D J</creator><creator>Cohn, S L</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20100427</creationdate><title>Criteria for evaluation of disease extent by 123I-metaiodobenzylguanidine scans in neuroblastoma: a report for the International Neuroblastoma Risk Group (INRG) Task Force</title><author>Matthay, K K ; Shulkin, B ; Ladenstein, R ; Michon, J ; Giammarile, F ; Lewington, V ; Pearson, A D J ; Cohn, S L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3421-326ec0c2555f9717fab5f68795fc9eeed19b37c549f457e8b584aaa62977b64c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>631/378/1689/1690</topic><topic>692/700/139/1677</topic><topic>692/700/1421/1771</topic><topic>692/700/1538</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Bone marrow</topic><topic>Cancer Research</topic><topic>Cancer therapies</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>full-paper</topic><topic>Guidelines</topic><topic>Medical prognosis</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Metastasis</topic><topic>Molecular Medicine</topic><topic>Nervous system</topic><topic>Neuroblastoma</topic><topic>Neurology</topic><topic>Nuclear medicine</topic><topic>Oncology</topic><topic>Pediatrics</topic><topic>Surveillance</topic><topic>Task forces</topic><topic>Tumors</topic><topic>Tumors of the nervous system. Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matthay, K K</creatorcontrib><creatorcontrib>Shulkin, B</creatorcontrib><creatorcontrib>Ladenstein, R</creatorcontrib><creatorcontrib>Michon, J</creatorcontrib><creatorcontrib>Giammarile, F</creatorcontrib><creatorcontrib>Lewington, V</creatorcontrib><creatorcontrib>Pearson, A D J</creatorcontrib><creatorcontrib>Cohn, S L</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS 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>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</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>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matthay, K K</au><au>Shulkin, B</au><au>Ladenstein, R</au><au>Michon, J</au><au>Giammarile, F</au><au>Lewington, V</au><au>Pearson, A D J</au><au>Cohn, S L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Criteria for evaluation of disease extent by 123I-metaiodobenzylguanidine scans in neuroblastoma: a report for the International Neuroblastoma Risk Group (INRG) Task Force</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><date>2010-04-27</date><risdate>2010</risdate><volume>102</volume><issue>9</issue><spage>1319</spage><epage>1326</epage><pages>1319-1326</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><coden>BJCAAI</coden><abstract>Background:
Neuroblastoma is an embryonic tumour of the sympathetic nervous system, metastatic in half of the patients at diagnosis, with a high preponderance of osteomedullary disease, making accurate evaluation of metastatic sites and response to therapy challenging. Metaiodobenzylguanidine (mIBG), taken into cells via the norepinephrine transporter, provides a sensitive and specific method of assessing tumour in both soft tissue and bone sites. The goal of this report was to develop consensus guidelines for the use of mIBG scans in staging, response assessment and surveillance in neuroblastoma.
Methods:
The International Neuroblastoma Risk Group (INRG) Task Force, including a multidisciplinary group in paediatric oncology of North and South America, Europe, Oceania and Asia, formed a subcommittee on metastatic disease evaluation, including expert nuclear medicine physicians and oncologists, who developed these guidelines based on their experience and the medical literature, with approval by the larger INRG Task Force.
Results:
Guidelines for patient preparation, radiotracer administration, techniques of scanning including timing, energy, specific views, and use of single photon emission computed tomography are included. Optimal timing of scans in relation to therapy and for surveillance is reviewed. Validated semi-quantitative scoring methods in current use are reviewed, with recommendations for use in prognosis and response evaluation.
Conclusions:
Metaiodobenzylguanidine scans are the most sensitive and specific method of staging and response evaluation in neuroblastoma, particularly when used with a semi-quantitative scoring method. Use of the optimal techniques for mIBG in staging and response, including a semi-quantitative score, is essential for evaluation of the efficacy of new therapy.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>20424613</pmid><doi>10.1038/sj.bjc.6605621</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/378/1689/1690 692/700/139/1677 692/700/1421/1771 692/700/1538 Biological and medical sciences Biomedical and Life Sciences Biomedicine Bone marrow Cancer Research Cancer therapies Drug Resistance Epidemiology full-paper Guidelines Medical prognosis Medical research Medical sciences Metastasis Molecular Medicine Nervous system Neuroblastoma Neurology Nuclear medicine Oncology Pediatrics Surveillance Task forces Tumors Tumors of the nervous system. Phacomatoses |
title | Criteria for evaluation of disease extent by 123I-metaiodobenzylguanidine scans in neuroblastoma: a report for the International Neuroblastoma Risk Group (INRG) Task Force |
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