Anti-BCMA Immuno-NanoPET Radiotracers for Improved Detection of Multiple Myeloma.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 34710281.
- Also identified by DOI 10.1002/adhm.202101565 and PMC identifier 11469021.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Current clinical imaging modalities for the sensitive and specific detection of multiple myeloma (MM) rely on nonspecific imaging contrast agents based on gadolinium chelates for magnetic resonance imaging (MRI) or for <sup>18</sup> F-FDG-directed and combined positron emission tomography (PET) and computed tomography (CT) scans. These tracers are not, however, able to detect minute plasma cell populations in the tumor niche, leading to false negative results. Here, a novel PET-based anti-BCMA nanoplatform labeled with <sup>64</sup> Cu is developed to improve the monitoring of these cells in both the spine and femur and to compare its sensitivity and specificity to more conventional immunoPET (<sup>64</sup> Cu labeled anti-BCMA antibody) and passively targeted PET radiotracers (<sup>64</sup> CuCl<sub>2</sub> and <sup>18</sup> F-FDG). This proof-of-concept preclinical study confirmed that by conjugating up to four times more radioisotopes per antibody with the immuno-nanoPET platform, an improvement in the sensitivity and in the specificity of PET to detect tumor cells in an orthotopic model of MM is observed when compared to the traditional immunoPET approach. It is anticipated that when combined with tumor biopsy, this immuno-nanoPET platform may improve the management of patients with MM.
Medical subject headings
- Multiple Myeloma