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Preclinical Evaluation of a 64Cu-Based Theranostic Approach in a Murine Model of Multiple Myeloma.
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.
Afiliación
  • Métivier C; Nantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, 44007 Nantes, France.
  • Le Saëc P; Nantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, 44007 Nantes, France.
  • Gaschet J; Nantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, 44007 Nantes, France.
  • Chauvet C; Nantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, 44007 Nantes, France.
  • Marionneau-Lambot S; Nantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, CHU Nantes, 44007 Nantes, France.
  • Hofgaard PO; Department of Immunology, Oslo University Hospital, 04024 Oslo, Norway.
  • Bogen B; Department of Immunology, Oslo University Hospital, 04024 Oslo, Norway.
  • Pineau J; Univ. Brest, UMR CNRS 6521 CEMCA, 6 Avenue Victor le Gorgeu, 29200 Brest, France.
  • Le Bris N; Univ. Brest, UMR CNRS 6521 CEMCA, 6 Avenue Victor le Gorgeu, 29200 Brest, France.
  • Tripier R; Univ. Brest, UMR CNRS 6521 CEMCA, 6 Avenue Victor le Gorgeu, 29200 Brest, France.
  • Alliot C; Nantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, 44007 Nantes, France.
  • Haddad F; GIP ARRONAX, 44800 Saint-Herblain, France.
  • Chérel M; IMT Atlantique, Nantes Université, Subatech, 44307 Nantes, France.
  • Chouin N; GIP ARRONAX, 44800 Saint-Herblain, France.
  • Faivre-Chauvet A; Nantes Université, Inserm, CNRS, Université d'Angers, CRCI2NA, 44007 Nantes, France.
  • Rbah-Vidal L; Nuclear Medicine Department, ICO-René Gauducheau Cancer Center, 44800 Saint-Herblain, France.
Pharmaceutics ; 15(7)2023 Jun 25.
Article en En | MEDLINE | ID: mdl-37514004
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 ß+ and ß- 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, [64Cu]Cu-TE1PA-9E7.4 in a MOPC315.BM mouse model of multiple myeloma. PET imaging using [64Cu]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 [64Cu]Cu-TE1PA-9E7.4 are safe and can be effective for TRT application in this syngeneic preclinical model of MM.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article País de afiliación: Francia