Preclinical Evaluation of a [sup.64]Cu-Based Theranostic Approach in a Murine Model of Multiple Myeloma
Although the concept of theranostics is neither new nor exclusive to nuclear medicine, it is a particularly promising approach for the future of nuclear oncology. This approach is based on the use of molecules targeting specific biomarkers in the tumour or its microenvironment, associated with optim...
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creator | Métivier, Cassandra Le Saëc, Patricia Gaschet, Joëlle Chauvet, Catherine Marionneau-Lambot, Séverine Hofgaard, Peter O Bogen, Bjarne Pineau, Julie Le Bris, Nathalie Tripier, Raphaël Alliot, Cyrille Haddad, Férid Chérel, Michel Chouin, Nicolas Faivre-Chauvet, Alain Rbah-Vidal, Latifa |
description | Although the concept of theranostics is neither new nor exclusive to nuclear medicine, it is a particularly promising approach for the future of nuclear oncology. This approach is based on the use of molecules targeting specific biomarkers in the tumour or its microenvironment, associated with optimal radionuclides which, depending on their emission properties, allow the combination of diagnosis by molecular imaging and targeted radionuclide therapy (TRT). Copper-64 has suitable decay properties (both β[sup.+] and β- decays) for PET imaging and potentially for TRT, making it both an imaging and therapy agent. We developed and evaluated a theranostic approach using a copper-64 radiolabelled anti-CD138 antibody, [[sup.64]Cu]Cu-TE1PA-9E7.4 in a MOPC315.BM mouse model of multiple myeloma. PET imaging using [[sup.64]Cu]Cu-TE1PA-9E7.4 allows for high-resolution PET images. Dosimetric estimation from ex vivo biodistribution data revealed acceptable delivered doses to healthy organs and tissues, and a very encouraging tumour absorbed dose for TRT applications. Therapeutic efficacy resulting in delayed tumour growth and increased survival without inducing major or irreversible toxicity has been observed with 2 doses of 35 MBq administered at a 2-week interval. Repeated injections of [[sup.64]Cu]Cu-TE1PA-9E7.4 are safe and can be effective for TRT application in this syngeneic preclinical model of MM. |
doi_str_mv | 10.3390/pharmaceutics15071817 |
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This approach is based on the use of molecules targeting specific biomarkers in the tumour or its microenvironment, associated with optimal radionuclides which, depending on their emission properties, allow the combination of diagnosis by molecular imaging and targeted radionuclide therapy (TRT). Copper-64 has suitable decay properties (both β[sup.+] and β- decays) for PET imaging and potentially for TRT, making it both an imaging and therapy agent. We developed and evaluated a theranostic approach using a copper-64 radiolabelled anti-CD138 antibody, [[sup.64]Cu]Cu-TE1PA-9E7.4 in a MOPC315.BM mouse model of multiple myeloma. PET imaging using [[sup.64]Cu]Cu-TE1PA-9E7.4 allows for high-resolution PET images. Dosimetric estimation from ex vivo biodistribution data revealed acceptable delivered doses to healthy organs and tissues, and a very encouraging tumour absorbed dose for TRT applications. Therapeutic efficacy resulting in delayed tumour growth and increased survival without inducing major or irreversible toxicity has been observed with 2 doses of 35 MBq administered at a 2-week interval. Repeated injections of [[sup.64]Cu]Cu-TE1PA-9E7.4 are safe and can be effective for TRT application in this syngeneic preclinical model of MM.</description><identifier>ISSN: 1999-4923</identifier><identifier>EISSN: 1999-4923</identifier><identifier>DOI: 10.3390/pharmaceutics15071817</identifier><language>eng</language><publisher>MDPI AG</publisher><subject>Ethylenediaminetetraacetic acid ; Multiple myeloma</subject><ispartof>Pharmaceutics, 2023-06, Vol.15 (7)</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Métivier, Cassandra</creatorcontrib><creatorcontrib>Le Saëc, Patricia</creatorcontrib><creatorcontrib>Gaschet, Joëlle</creatorcontrib><creatorcontrib>Chauvet, Catherine</creatorcontrib><creatorcontrib>Marionneau-Lambot, Séverine</creatorcontrib><creatorcontrib>Hofgaard, Peter O</creatorcontrib><creatorcontrib>Bogen, Bjarne</creatorcontrib><creatorcontrib>Pineau, Julie</creatorcontrib><creatorcontrib>Le Bris, Nathalie</creatorcontrib><creatorcontrib>Tripier, Raphaël</creatorcontrib><creatorcontrib>Alliot, Cyrille</creatorcontrib><creatorcontrib>Haddad, Férid</creatorcontrib><creatorcontrib>Chérel, Michel</creatorcontrib><creatorcontrib>Chouin, Nicolas</creatorcontrib><creatorcontrib>Faivre-Chauvet, Alain</creatorcontrib><creatorcontrib>Rbah-Vidal, Latifa</creatorcontrib><title>Preclinical Evaluation of a [sup.64]Cu-Based Theranostic Approach in a Murine Model of Multiple Myeloma</title><title>Pharmaceutics</title><description>Although the concept of theranostics is neither new nor exclusive to nuclear medicine, it is a particularly promising approach for the future of nuclear oncology. This approach is based on the use of molecules targeting specific biomarkers in the tumour or its microenvironment, associated with optimal radionuclides which, depending on their emission properties, allow the combination of diagnosis by molecular imaging and targeted radionuclide therapy (TRT). Copper-64 has suitable decay properties (both β[sup.+] and β- decays) for PET imaging and potentially for TRT, making it both an imaging and therapy agent. We developed and evaluated a theranostic approach using a copper-64 radiolabelled anti-CD138 antibody, [[sup.64]Cu]Cu-TE1PA-9E7.4 in a MOPC315.BM mouse model of multiple myeloma. PET imaging using [[sup.64]Cu]Cu-TE1PA-9E7.4 allows for high-resolution PET images. Dosimetric estimation from ex vivo biodistribution data revealed acceptable delivered doses to healthy organs and tissues, and a very encouraging tumour absorbed dose for TRT applications. Therapeutic efficacy resulting in delayed tumour growth and increased survival without inducing major or irreversible toxicity has been observed with 2 doses of 35 MBq administered at a 2-week interval. Repeated injections of [[sup.64]Cu]Cu-TE1PA-9E7.4 are safe and can be effective for TRT application in this syngeneic preclinical model of MM.</description><subject>Ethylenediaminetetraacetic acid</subject><subject>Multiple myeloma</subject><issn>1999-4923</issn><issn>1999-4923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptjk1LAzEQhoMoWGp_ghDwvDXZ7EdyrKV-QBc91JNImU1m20h2s2x2Bf-9ET304MxhhpfnfWcIueZsKYRit_0RhhY0TqPVgees5JKXZ2TGlVJJplJxfrJfkkUIHyyWEFwKNSOHlwG1s53V4OjmE9wEo_Ud9Q0F-hamfllk7-spuYOAhu6OOEDnQ7xFV30_eNBHaruIVtNgO6SVN-h-zNXkRtu7qHyh8y1ckYsGXMDF35yT1_vNbv2YbJ8fntarbXLgohwTCVktco1MYhEfrHWeNoqhwpoXRgMII0yd1kzLTPG6KCCFjHGZGimMrrUSc3Lzm3sAh3vbNX4cQLc26P2qzBWXqixlpJb_ULENtlb7Dhsb9RPDN19cbRQ</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Métivier, Cassandra</creator><creator>Le Saëc, Patricia</creator><creator>Gaschet, Joëlle</creator><creator>Chauvet, Catherine</creator><creator>Marionneau-Lambot, Séverine</creator><creator>Hofgaard, Peter O</creator><creator>Bogen, Bjarne</creator><creator>Pineau, Julie</creator><creator>Le Bris, Nathalie</creator><creator>Tripier, Raphaël</creator><creator>Alliot, Cyrille</creator><creator>Haddad, Férid</creator><creator>Chérel, Michel</creator><creator>Chouin, Nicolas</creator><creator>Faivre-Chauvet, Alain</creator><creator>Rbah-Vidal, Latifa</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20230601</creationdate><title>Preclinical Evaluation of a [sup.64]Cu-Based Theranostic Approach in a Murine Model of Multiple Myeloma</title><author>Métivier, Cassandra ; Le Saëc, Patricia ; Gaschet, Joëlle ; Chauvet, Catherine ; Marionneau-Lambot, Séverine ; Hofgaard, Peter O ; Bogen, Bjarne ; Pineau, Julie ; Le Bris, Nathalie ; Tripier, Raphaël ; Alliot, Cyrille ; Haddad, Férid ; Chérel, Michel ; Chouin, Nicolas ; Faivre-Chauvet, Alain ; Rbah-Vidal, Latifa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g137t-8a4b35ce08e6183bc52f90e9eb16dcaa3d3db2b0c8491b66a2a40182d83dcbc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Ethylenediaminetetraacetic acid</topic><topic>Multiple myeloma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Métivier, Cassandra</creatorcontrib><creatorcontrib>Le Saëc, Patricia</creatorcontrib><creatorcontrib>Gaschet, Joëlle</creatorcontrib><creatorcontrib>Chauvet, Catherine</creatorcontrib><creatorcontrib>Marionneau-Lambot, Séverine</creatorcontrib><creatorcontrib>Hofgaard, Peter O</creatorcontrib><creatorcontrib>Bogen, Bjarne</creatorcontrib><creatorcontrib>Pineau, Julie</creatorcontrib><creatorcontrib>Le Bris, Nathalie</creatorcontrib><creatorcontrib>Tripier, Raphaël</creatorcontrib><creatorcontrib>Alliot, Cyrille</creatorcontrib><creatorcontrib>Haddad, Férid</creatorcontrib><creatorcontrib>Chérel, Michel</creatorcontrib><creatorcontrib>Chouin, Nicolas</creatorcontrib><creatorcontrib>Faivre-Chauvet, Alain</creatorcontrib><creatorcontrib>Rbah-Vidal, Latifa</creatorcontrib><jtitle>Pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Métivier, Cassandra</au><au>Le Saëc, Patricia</au><au>Gaschet, Joëlle</au><au>Chauvet, Catherine</au><au>Marionneau-Lambot, Séverine</au><au>Hofgaard, Peter O</au><au>Bogen, Bjarne</au><au>Pineau, Julie</au><au>Le Bris, Nathalie</au><au>Tripier, Raphaël</au><au>Alliot, Cyrille</au><au>Haddad, Férid</au><au>Chérel, Michel</au><au>Chouin, Nicolas</au><au>Faivre-Chauvet, Alain</au><au>Rbah-Vidal, Latifa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preclinical Evaluation of a [sup.64]Cu-Based Theranostic Approach in a Murine Model of Multiple Myeloma</atitle><jtitle>Pharmaceutics</jtitle><date>2023-06-01</date><risdate>2023</risdate><volume>15</volume><issue>7</issue><issn>1999-4923</issn><eissn>1999-4923</eissn><abstract>Although the concept of theranostics is neither new nor exclusive to nuclear medicine, it is a particularly promising approach for the future of nuclear oncology. This approach is based on the use of molecules targeting specific biomarkers in the tumour or its microenvironment, associated with optimal radionuclides which, depending on their emission properties, allow the combination of diagnosis by molecular imaging and targeted radionuclide therapy (TRT). Copper-64 has suitable decay properties (both β[sup.+] and β- decays) for PET imaging and potentially for TRT, making it both an imaging and therapy agent. We developed and evaluated a theranostic approach using a copper-64 radiolabelled anti-CD138 antibody, [[sup.64]Cu]Cu-TE1PA-9E7.4 in a MOPC315.BM mouse model of multiple myeloma. PET imaging using [[sup.64]Cu]Cu-TE1PA-9E7.4 allows for high-resolution PET images. Dosimetric estimation from ex vivo biodistribution data revealed acceptable delivered doses to healthy organs and tissues, and a very encouraging tumour absorbed dose for TRT applications. Therapeutic efficacy resulting in delayed tumour growth and increased survival without inducing major or irreversible toxicity has been observed with 2 doses of 35 MBq administered at a 2-week interval. Repeated injections of [[sup.64]Cu]Cu-TE1PA-9E7.4 are safe and can be effective for TRT application in this syngeneic preclinical model of MM.</abstract><pub>MDPI AG</pub><doi>10.3390/pharmaceutics15071817</doi></addata></record> |
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subjects | Ethylenediaminetetraacetic acid Multiple myeloma |
title | Preclinical Evaluation of a [sup.64]Cu-Based Theranostic Approach in a Murine Model of Multiple Myeloma |
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