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Biodistribution and Radiation Dosimetry for [68Ga]Ga-LNTH-1363S, a Probe Targeting Fibroblast Activation Protein α
Johanna S Enke1,2, Bradley W Schuller3, Lisa Glantschnig1
1Nuclear Medicine, Faculty of Medicine, University of Augsburg, Augsburg, Germany.
Summary
This study shows that the new fibroblast activation protein (FAP)-targeted tracer [68Ga]Ga-LNTH-1363S has good tumor uptake and clearance in cancer patients. Its radiation dosimetry is favorable, making it a promising PET imaging agent.
Area of Science:
- Nuclear Medicine
- Radiochemistry
- Oncology
Background:
- Fibroblast Activation Protein (FAP) is a key target in cancer imaging.
- [68Ga]Ga-LNTH-1363S is a novel positron emission tomography (PET) tracer designed for FAP targeting.
Purpose of the Study:
- To evaluate the PET biodistribution and radiation dosimetry of [68Ga]Ga-LNTH-1363S in cancer patients.
- To assess the safety and efficacy of this new FAP-targeted tracer.
Main Methods:
- Five cancer patients received [68Ga]Ga-LNTH-1363S (153-184 MBq) intravenously.
- PET/CT imaging was performed at 10, 60, and 180 minutes post-injection.
- Radiation dosimetry was calculated using the MIRD formalism, and SUV analysis was conducted.
Main Results:
- The tracer showed rapid tumor uptake and efficient clearance from non-target tissues, yielding high tumor-to-background ratios.
- The kidneys received the highest absorbed dose (0.038 ± 0.01 mGy/MBq).
- Tumor SUVmax peaked at 10 minutes (18.6 ± 7.2) and remained high; effective dose was 0.013 ± 0.002 mSv/MBq.
Conclusions:
- [68Ga]Ga-LNTH-1363S exhibits favorable biodistribution and dosimetry profiles for PET imaging.
- Its performance is comparable to other FAP-targeted tracers.
- The tracer is a promising candidate for FAP-targeted cancer imaging.
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