Radioiodinated N-[3-(4-morpholino)propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9) : a new potential melanoma imaging agent
The role of nuclear medicine in the management of patients with malignant melanoma has expanded in recent years with the introduction of lymphoscintigraphy and sentinel lymph node biopsy, intense interest in positron emission tomography (PET) imaging using 2-[18F]fluoro-2-deoxyglucose (18F-FDG) as a...
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Veröffentlicht in: | European Journal of Nuclear Medicine 2001-04, Vol.28 (4), p.408-417 |
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description | The role of nuclear medicine in the management of patients with malignant melanoma has expanded in recent years with the introduction of lymphoscintigraphy and sentinel lymph node biopsy, intense interest in positron emission tomography (PET) imaging using 2-[18F]fluoro-2-deoxyglucose (18F-FDG) as a tracer, and encouraging reports of several new single-photon-emitting radiopharmaceuticals. While PET imaging with FDG exhibits a high sensitivity for imaging patients with melanoma, specificity may not be as high and access to the technology remains limited. Single-photon emission tomography (SPET) imaging remains standard technology for most nuclear medicine departments. We report a novel radiopharmaceutical--radioiodinated N-[3-(4-morpholino)-propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9)--which appears to show a sensitivity and specificity that are commensurate with expectations of a radiopharmaceutical for routine clinical imaging. In this phase II trial, 110 patients at risk for recurrence, with suspected recurrence or being restaged have been imaged with this novel tracer, demonstrating an overall sensitivity of 91% and specificity of 89%. The results of our study support a phase III trial to establish the clinical role of ERC9 in staging melanoma patients at presentation who are at high risk for metastasis, or restaging patients with known relapse to assess the extent of their disease, particularly if therapy or enrollment into a clinical trial is being considered. |
doi_str_mv | 10.1007/s002590000455 |
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We report a novel radiopharmaceutical--radioiodinated N-[3-(4-morpholino)-propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9)--which appears to show a sensitivity and specificity that are commensurate with expectations of a radiopharmaceutical for routine clinical imaging. In this phase II trial, 110 patients at risk for recurrence, with suspected recurrence or being restaged have been imaged with this novel tracer, demonstrating an overall sensitivity of 91% and specificity of 89%. The results of our study support a phase III trial to establish the clinical role of ERC9 in staging melanoma patients at presentation who are at high risk for metastasis, or restaging patients with known relapse to assess the extent of their disease, particularly if therapy or enrollment into a clinical trial is being considered.</description><identifier>ISSN: 0340-6997</identifier><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s002590000455</identifier><identifier>PMID: 11357490</identifier><identifier>CODEN: EJNMD9</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Benzylamines ; Biological and medical sciences ; Bone Neoplasms - diagnostic imaging ; Bone Neoplasms - secondary ; Female ; General aspects ; Humans ; Image Processing, Computer-Assisted ; Lymphatic Metastasis - diagnostic imaging ; Male ; Medical sciences ; Melanoma - diagnostic imaging ; Middle Aged ; Morpholines ; Radiopharmaceuticals ; Recurrence ; Tissue Distribution ; Tomography, Emission-Computed, Single-Photon ; Tomography, X-Ray Computed ; Tumors</subject><ispartof>European Journal of Nuclear Medicine, 2001-04, Vol.28 (4), p.408-417</ispartof><rights>2001 INIST-CNRS</rights><rights>Springer-Verlag 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-4ba4070230d99ccddd2390df2869ba4b92d50df6563401185dd20defbb5ab17f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=943153$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11357490$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SALOPEK, Thomas G</creatorcontrib><creatorcontrib>SCOTT, John R</creatorcontrib><creatorcontrib>JOSHUA, Alummoottil V</creatorcontrib><creatorcontrib>SMYLIE, Michael</creatorcontrib><creatorcontrib>LOGUS, J. Wayne</creatorcontrib><creatorcontrib>MORIN, Carrie A</creatorcontrib><creatorcontrib>MCEWAN, Alexander J. B</creatorcontrib><title>Radioiodinated N-[3-(4-morpholino)propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9) : a new potential melanoma imaging agent</title><title>European Journal of Nuclear Medicine</title><addtitle>Eur J Nucl Med</addtitle><description>The role of nuclear medicine in the management of patients with malignant melanoma has expanded in recent years with the introduction of lymphoscintigraphy and sentinel lymph node biopsy, intense interest in positron emission tomography (PET) imaging using 2-[18F]fluoro-2-deoxyglucose (18F-FDG) as a tracer, and encouraging reports of several new single-photon-emitting radiopharmaceuticals. While PET imaging with FDG exhibits a high sensitivity for imaging patients with melanoma, specificity may not be as high and access to the technology remains limited. Single-photon emission tomography (SPET) imaging remains standard technology for most nuclear medicine departments. We report a novel radiopharmaceutical--radioiodinated N-[3-(4-morpholino)-propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9)--which appears to show a sensitivity and specificity that are commensurate with expectations of a radiopharmaceutical for routine clinical imaging. In this phase II trial, 110 patients at risk for recurrence, with suspected recurrence or being restaged have been imaged with this novel tracer, demonstrating an overall sensitivity of 91% and specificity of 89%. The results of our study support a phase III trial to establish the clinical role of ERC9 in staging melanoma patients at presentation who are at high risk for metastasis, or restaging patients with known relapse to assess the extent of their disease, particularly if therapy or enrollment into a clinical trial is being considered.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Benzylamines</subject><subject>Biological and medical sciences</subject><subject>Bone Neoplasms - diagnostic imaging</subject><subject>Bone Neoplasms - secondary</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Lymphatic Metastasis - diagnostic imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melanoma - diagnostic imaging</subject><subject>Middle Aged</subject><subject>Morpholines</subject><subject>Radiopharmaceuticals</subject><subject>Recurrence</subject><subject>Tissue Distribution</subject><subject>Tomography, Emission-Computed, Single-Photon</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors</subject><issn>0340-6997</issn><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkV9LHDEUxUNRdLV97KsEBNGH1GSSzGz6VhZbBVGQ9qmUITPJ7EYyyZjMotMv4NfuFRf_NC8hnF_uvecehD4z-oVRWp1mSgupKBwh5Qc0YyVTpKJztYVmlAtKSqWqXbSX8-0TI7jcQbuMcVkJRWfo8UYbF100LujRGnxFfnNyLEgf07CK3oV4MqQ4TP4PuSK9HVeTJwVZTSbFh4lIAj8j4RulseHv5HXvgsXHZzcLdYK_Yo2DvcdDHG0Ynfa4t16H2Gvser10YYn1EpSPaLvTPttPm3sf_fp-9nNxTi6vf1wsvl2Slgs5EtFoQStacGqUaltjTMEVNV0xLxVIjSqMhGcpS7DO2FwCQI3tmkbqhlUd30dHz3XB1d3a5rHuXW6th5lsXOcaNieVnHMAD_8Db-M6BZitZrQoK9glV0CRZ6pNMedku3pI4CtNANVP-dTv8gH-YFN13fTWvNKbQN601bnVvks6tC6_cEpwJjn_B_Y-lkM</recordid><startdate>20010401</startdate><enddate>20010401</enddate><creator>SALOPEK, Thomas G</creator><creator>SCOTT, John R</creator><creator>JOSHUA, Alummoottil V</creator><creator>SMYLIE, Michael</creator><creator>LOGUS, J. 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B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radioiodinated N-[3-(4-morpholino)propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9) : a new potential melanoma imaging agent</atitle><jtitle>European Journal of Nuclear Medicine</jtitle><addtitle>Eur J Nucl Med</addtitle><date>2001-04-01</date><risdate>2001</risdate><volume>28</volume><issue>4</issue><spage>408</spage><epage>417</epage><pages>408-417</pages><issn>0340-6997</issn><issn>1619-7070</issn><eissn>1619-7089</eissn><coden>EJNMD9</coden><abstract>The role of nuclear medicine in the management of patients with malignant melanoma has expanded in recent years with the introduction of lymphoscintigraphy and sentinel lymph node biopsy, intense interest in positron emission tomography (PET) imaging using 2-[18F]fluoro-2-deoxyglucose (18F-FDG) as a tracer, and encouraging reports of several new single-photon-emitting radiopharmaceuticals. While PET imaging with FDG exhibits a high sensitivity for imaging patients with melanoma, specificity may not be as high and access to the technology remains limited. Single-photon emission tomography (SPET) imaging remains standard technology for most nuclear medicine departments. We report a novel radiopharmaceutical--radioiodinated N-[3-(4-morpholino)-propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9)--which appears to show a sensitivity and specificity that are commensurate with expectations of a radiopharmaceutical for routine clinical imaging. In this phase II trial, 110 patients at risk for recurrence, with suspected recurrence or being restaged have been imaged with this novel tracer, demonstrating an overall sensitivity of 91% and specificity of 89%. The results of our study support a phase III trial to establish the clinical role of ERC9 in staging melanoma patients at presentation who are at high risk for metastasis, or restaging patients with known relapse to assess the extent of their disease, particularly if therapy or enrollment into a clinical trial is being considered.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>11357490</pmid><doi>10.1007/s002590000455</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Benzylamines Biological and medical sciences Bone Neoplasms - diagnostic imaging Bone Neoplasms - secondary Female General aspects Humans Image Processing, Computer-Assisted Lymphatic Metastasis - diagnostic imaging Male Medical sciences Melanoma - diagnostic imaging Middle Aged Morpholines Radiopharmaceuticals Recurrence Tissue Distribution Tomography, Emission-Computed, Single-Photon Tomography, X-Ray Computed Tumors |
title | Radioiodinated N-[3-(4-morpholino)propyl]-N-methyl-2-hydroxy-5-iodo-3-methylbenzylamine (ERC9) : a new potential melanoma imaging agent |
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