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An Automated Radiosynthesis of [68Ga]Ga-FAPI-46 for Routine Clinical Use
Published on: May 24, 2024
RADIOPHARMACEUTICALS BASED ON FIBROBLAST ACTIVATION PROTEIN INHIBITORS IN ONCOLOGICAL PRACTICE
1Nonprofit Organization National Cancer Institute of Ministry of Health of Ukraine, 33/43 Julia Zdanovska Str., Kyiv, 03022, Ukraine.
Abstract:
The review is devoted to the application of the new perspective class of radionuclide tracers, based on inhibitors of the fibroblast activation protein (FAP), which is a marker of cancer-associated fibroblasts of microenvironment of most malignant tumors. FAP inhibitors (FAPI) can be labeled by a wide spectrum of radionuclides, which can provide both radionuclide diagnostics and radionuclide therapy. It was showed, that the diagnostic efficacy of FAPI positron emission tomography/computed tomography (PET/CT) in various cancers is similar to 18F-fluorodesoxyglu-cose-PET/CT or superior. The FAPI radiopharmaceuticals (RP) have some advantage compared to 18F-fluorodesoxy-glucose (FDG): no need for special preparation and diet, fast imaging with high contrast, and increased sensitivity in region with high glucose metabolism. FAPI-PET/CT may be an important addition to conventional methods in all stages of diagnostic process in oncology, especially when 18F-FDG cannot be used. It is need to further wide prospective investigations for assessing of diagnostic efficacy of FAPI-RP and determination of indications for its using.
Insights
New fibroblast activation protein (FAP) inhibitors as radionuclide tracers show diagnostic efficacy in various cancers, comparable or superior to 18F-FDG PET/CT. These FAP inhibitors offer advantages for cancer diagnostics and therapy.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiopharmaceutical Chemistry
Background:
- Fibroblast activation protein (FAP) is a marker of cancer-associated fibroblasts in the tumor microenvironment.
- FAP inhibitors (FAPI) represent a novel class of radionuclide tracers with potential for both diagnosis and therapy.
- Current diagnostic methods like 18F-FDG PET/CT have limitations.
Purpose of the Study:
- To review the application of FAP inhibitors as radionuclide tracers in oncology.
- To evaluate the diagnostic efficacy of FAPI-based positron emission tomography/computed tomography (PET/CT) compared to existing methods.
- To explore the advantages of FAPI radiopharmaceuticals (RP) in cancer diagnostics.
Main Methods:
- Review of existing literature on FAP inhibitors and their application in radionuclide imaging.
- Comparison of diagnostic performance of FAPI PET/CT with 18F-fluorodeoxyglucose (FDG) PET/CT.
- Analysis of FAPI radiopharmaceuticals' characteristics and potential benefits.
Main Results:
- FAPI can be labeled with various radionuclides for diagnostic and therapeutic purposes.
- FAPI PET/CT demonstrates diagnostic efficacy similar to or superior to 18F-FDG PET/CT in diverse cancers.
- FAPI RP offer advantages over 18F-FDG, including no special preparation, fast imaging, high contrast, and increased sensitivity in certain metabolic regions.
Conclusions:
- FAPI PET/CT is a promising addition to conventional oncology diagnostics across all stages.
- FAPI PET/CT can be particularly valuable when 18F-FDG is unsuitable.
- Further prospective studies are needed to fully assess FAPI RP efficacy and establish clinical indications.
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