In spite of an enormous global research effort, astonishing preclinical cancer cures, and the approval of multiple formulations, nanomedicine’s impact on cancer patient care remains limited. Recently, it is becoming evident that this unsatisfactory exploitation may be tackled by considering nanodrugs’ extensive interaction with the immune system. Moreover, our collaborators recently demonstrated these interactions can be tuned and potentially utilized in (immuno)therapeutic settings.
At the same time, immunotherapy is rapidly developing into a powerful therapeutic modality in oncology. Nonetheless, it is now well-established that only a portion of treated patients respond and combination therapies are anticipated to greatly improve immunotherapeutic outcomes. In such synergistic therapeutic regimens, one component may serve to ‘prime’ patients for immunotherapy, for example through immune cell activation, or immune system rebalancing.
The innate immune system is emerging as an important regulator of anti-cancer adaptive immune responses; numerous mechanisms through which phagocytes and other innate immune cells can regulate anti-tumor immune responses are being discovered. Technology allowing for detection and imaging of these dynamic processes in patients will greatly benefit (immune)therapy selection and monitoring. Moreover, interference in these phagocyte specific pathways may be a potent approach to improve anti-cancer immune responses and boost immunotherapy.
In preliminary work for this project we have established that certain nanoparticles are specifically and extensively taken up by phagocytes. Now, in the “coastal collaboration”, we aim to develop these nanoparticles into diagnostic PET imaging and therapeutic agents in breast cancer. This will be facilitated by the integrative application of advanced in vivo imaging methods, including PET, MRI, and intravital microscopy, in conjunction with uniquely complementary and state-of-the-art ex vivo immune response and cell profiling methodology. Being part of the coastal collaboration offers exciting opportunities for interdisciplinary collaboration, validation of results, and free exchange of mutually beneficial tracers and protocols.
WP1: Immuno-PET and lung cancer
Despite the demonstrated effectiveness of immunoregulatory agents such as immune checkpoint blockers (ICB) on refractory cancers, these therapies work satisfactorily only in a reduced subset of patients. Further, ICB treatments are not exempt of risks and are associated to very high costs. Reliable response biomarkers are needed to identify responders and non-responders, and conventional imaging…
WP2: Radionuclide targeted therapy and imaging in Glioblastoma
The plasticity of GB tumor cells and their ability to infiltrate adjoining brain tissue limits the effectiveness of current cancer therapies. Microglia plays an important role in GB progression. Inhibition of EGFR and CSF-1R decreases microglia-stimulated invasion of GB cells. Specific radiopharmaceuticals targeting EGFR or CSF-1R will be developed (WP3/Bergen) and applied as (i) diagnostic…
WP3: Phagocyte targeting in breast cancer
In spite of an enormous global research effort, astonishing preclinical cancer cures, and the approval of multiple formulations, nanomedicine’s impact on cancer patient care remains limited. Recently, it is becoming evident that this unsatisfactory exploitation may be tackled by considering nanodrugs’ extensive interaction with the immune system. Moreover, our collaborators recently demonstrated these interactions can…
WP4: Advancing oncological PET imaging using machine learning
The work package on machine learning will develop data analysis methods in support of the other work packages. The aim is to use expertise in artificial intelligence to help solving the medical research questions in the 180° North project. Our work focuses in particular on how to fuse the information from data acquisitions with PET,…