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An Automated Radiosynthesis of [68Ga]Ga-FAPI-46 for Routine Clinical Use
Published on: May 24, 2024
Exploring the Diagnostic Utility of 68 Ga-FAPI-46 PET/CT in Diverse Pulmonary Pathologies : A Comparative Analysis
Priyavrat Purohit1, Piyush Aggarwal1, Rajender Kumar1
1Departments of Nuclear Medicine.
68Ga-Fibroblast activation protein inhibitor (FAPI) PET shows promise for lung lesion characterization, offering an alternative to 18F-FDG PET. However, careful interpretation is needed due to potential false positives and negatives, requiring histopathologic confirmation.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiochemistry
Background:
- Lung cancer is a leading global cause of cancer mortality.
- Distinguishing benign from malignant lung lesions is challenging with conventional imaging like CT and 18F-FDG PET.
- Novel PET tracers are being investigated for improved diagnostic accuracy.
Purpose of the Study:
- To prospectively compare the efficacy of 68Ga-FAPI-46 PET and 18F-FDG PET in characterizing lung lesions.
- To evaluate the diagnostic performance of both tracers in differentiating benign from malignant lung nodules.
Main Methods:
- Patients with suspected lung lesions underwent both 68Ga-FAPI-46 PET/CT and 18F-FDG PET/CT scans.
- Histopathology was used to classify lesions as benign or malignant.
- Semi-quantitative analysis (SUVmax) and ROC analysis were performed to determine optimal cut-offs for differentiation.
Main Results:
- Sixty-six patients with 14 benign and 52 malignant lesions were analyzed.
- Median SUVmax values for benign and malignant lesions were significantly different for both 68Ga-FAPI (9.8 vs. 14.7, P=0.002) and 18F-FDG (8.8 vs. 13.5, P=0.001).
- ROC analysis yielded SUVmax cut-offs of 12.2 (AUC=0.77) for 68Ga-FAPI and 9.5 (AUC=0.78) for 18F-FDG.
Conclusions:
- 68Ga-FAPI-46 PET/CT demonstrates potential as an alternative imaging modality for lung lesion characterization.
- The tracer requires cautious interpretation due to potential false positives in benign lesions and false negatives in low-grade tumors.
- Histopathologic confirmation remains essential for definitive diagnosis.
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