

Our Research.
Our lab is dedicated to pioneering advanced cancer therapies through innovative research.
Radioligand therapy (RLT) is based on the specificity of ligands that bind to receptors or antigens on cancer cells, delivering targeted radiation to induce cell death while sparing healthy tissues. Several receptors and ligands have been investigated in RLT in order to widen the spectrum of treatable cancers and increase treatment efficacy while maintaining tolerability. The challenges yet to be overcome are many, for example, radioresistance, tumor heterogeneity, suboptimal pharmacokinetics, as well as real-world feasibility.
Beyond Peptide Receptor Radionuclide Therapy (PRRT) to treat SSTR-positive tumors using radiolabeled peptides and Prostate-Specific Membrane Antigen (PSMA)-targeted RLT to treat metastatic castration-resistant prostate cancer, our areas of research include investigating new targets, finding new targeting, drug-delivery or pharmacokinetics-improving mechanisms, and exploring a variety of suitable radionuclides including the potential of alpha-emitter therapy. For example, Fibroblast Activation Protein (FAP) has been heavily researched for its role in various solid cancers, with ligands such as FAP inhibitors FAPIs used in imaging and potential therapeutic applications. Our team has
extensively published results on ways to improve FAPIs, including preliminary results of 177Lu-EB-FAPI therapy, contributing to the growing body of research supporting FAP-targeted theranostics.
Developing new radiotracers that target specific biomarkers or molecular pathways will enable earlier and more accurate diagnosis, as well as better monitoring of treatment response. Our motive for researching RLT stems from the need to improve patient outcomes, including survival and quality of life.