These two novel radiopharmaceuticals were developed for theragnostic use, i.e. molecular imaging and treatment. Each targets a different biological marker: 68Ga-NeoB targets the gastrin-releasing peptide receptor (GRPR) and 68Ga-PSMA-R2 targets prostate-specific membrane antigen (PSMA); both molecular markers are known to be overexpressed in prostate cancer.
Both 68Ga-NeoB and 68Ga-PSMA-R2 were feasible and safe for diagnostic imaging. 68Ga-NeoB outperformed 68Ga-PSMA-R2 PET/MRI with higher detection rates on a per-patient and per-lesion basis, particularly in detecting bone and lymph node metastases at lower PSA levels. Higher sensitivity, accuracy, and negative predictive value were seen with 68Ga-NeoB while specificity and positive predictive value were equally high for both radiopharmaceuticals.
The biodistribution of 68Ga-NeoB with improved affinity to GRPR was more favorable for theragnostic use than 68Ga-PSMA-R2, which showed overall lower tumor uptake and tumor-to-background ratio. Although PSMA-targeted PET imaging is the most commonly and widely used, GRPR-targeted PET imaging presents a complementary or alternative option. Prostate cancer has a heterogeneous biology, therefore, the more biological targets we have, the better care we can provide for our patients.
Written by: Heying Duan,1 Hong Song,1 Guido A Davidzon,1 Farshad Moradi,1 Tie Liang,1 Andreas Loening,2 Shreyas Vasanawala,2 Andrei Iagaru,1
- Division of Nuclear Medicine and Molecular Imaging, Department of Radiology, Stanford University, Stanford, California
- Division of Body MRI, Department of Radiology, Stanford University, Stanford, California.
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