[<sup>64</sup>Cu]Cu-NOTA-EV-F(ab')<sub>2</sub> Enables Same-Day Immuno-PET Imaging of Nectin-4 in Triple-Negative Breast and Urothelial Bladder Cancers.
Where this comes from
- Record sourced from PubMed, PMID 40774696.
- Also identified by DOI 10.2967/jnumed.125.270132 and PMC identifier 12410301.
- 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
Our study aimed to develop and evaluate [<sup>64</sup>Cu]Cu-NOTA-EV-F(ab')<sub>2</sub> for immuno-PET imaging of nectin-4 expression in triple-negative breast cancer (TNBC) and urothelial bladder cancer (UBC) models, with the goal of achieving rapid, specific tumor targeting and high tumor-to-background contrast. <b>Methods:</b> Bivalent antibody fragments were generated from enfortumab vedotin (EV) using IdeS protease and conjugated with NOTA for radiolabeling with <sup>64</sup>Cu. In vitro binding and uptake studies were performed using TNBC and UBC cell lines. Immuno-PET imaging and biodistribution studies were conducted in athymic nude mice bearing subcutaneous xenografts with varying nectin-4 expression. <b>Results:</b> [<sup>64</sup>Cu]Cu-NOTA-EV-F(ab')<sub>2</sub> exhibited rapid tumor accumulation and high specificity in nectin-4-positive tumors, with peak uptake observed at 4 h after injection. EV-F(ab')<sub>2</sub> demonstrated superior tumor-to-background ratios compared with the full-length EV antibody, particularly in nectin-4-expressing models (MDA-MB-468, BT474, SW780, and HT-1376). Blocking studies confirmed nectin-4-specific targeting. Favorable pharmacokinetics of EV-F(ab')<sub>2</sub> allowed for same-day imaging and reduced radiation exposure relative to intact antibodies. <b>Conclusion:</b> [<sup>64</sup>Cu]Cu-NOTA-EV-F(ab')<sub>2</sub> is a promising immuno-PET probe for assessing nectin-4 expression in TNBC and UBC.
Medical subject headings
- Copper Radioisotopes
- Cell Adhesion Molecules
- Urinary Bladder Neoplasms
- Triple Negative Breast Neoplasms
- Positron-Emission Tomography
- Heterocyclic Compounds, 1-Ring
- Immunoglobulin Fab Fragments