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Article Abstract

Multiple myeloma (MM) is the second most prevalent hematological malignancy. It remains incurable despite the availability of novel therapeutic approaches, marking an urgent need for new agents for noninvasive targeted imaging of MM lesions. CD38 has proven to be an excellent biomarker due to its high expression in aberrant lymphoid and myeloid cells relative to normal cell populations. Using isatuximab (Sanofi), the latest FDA-approved CD38-targeting antibody, we have developed Zirconium-89(Zr)-labeled isatuximab as a novel immunoPET tracer for the delineation of MM and evaluated the extension of its applicability to lymphomas. studies validated the high binding affinity and specificity of Zr-DFO-isatuximab for CD38. PET imaging demonstrated the high performance of Zr-DFO-isatuximab as a targeted imaging agent to delineate tumor burden in disseminated models of MM and Burkitt's lymphoma. biodistribution studies confirmed that high accumulations of the tracer in bone marrow and bone skeleton correspond to specific disease lesions as they are reduced to background in blocking and healthy controls. This work demonstrates the promise of Zr-DFO-isatuximab as an immunoPET tracer for CD38-targeted imaging of MM and certain lymphomas. More importantly, its potential as an alternative to Zr-DFO-daratumumab holds great clinical relevance.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308590PMC
http://dx.doi.org/10.1021/acsomega.3c00624DOI Listing

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