Accurate diagnosis and staging are crucial for selecting treatment for patients with pancreatic ductal
adenocarcinoma (PDAC). The desmoplastic responses associated with PDAC are often characterized by hypometabolism. Here, we investigated 18F-fibroblast activation
protein inhibitor (FAPI)-04 PET/CT in evaluation of PDAC and compared the findings with those obtained using
18F-FDG. Methods: Sixty-two PDAC patients underwent 18F-FAPI-04 PET/CT and
18F-FDG PET/CT. Identification of primary lesions, lymph node (LN)
metastasis, and distant
metastasis (DM) by these methods was evaluated, and TNM staging was performed. Correlation between SUVmax of the primary lesion and treatment response was explored in patients who received systemic
therapy. Results: 18F-FAPI-04 PET/CT identified all patients with PDAC;
18F-FDG PET/CT missed 1 patient. Tracer uptake was higher in 18F-FAPI-04 PET/CT than in
18F-FDG PET/CT in primary
tumors (10.63 vs. 2.87, P < 0.0001), LN
metastasis (2.90 vs. 1.43, P < 0.0001), and DM (liver, 6.11 vs. 3.10, P = 0.002; peritoneal, 4.70 vs. 2.08, P = 0.015). The methods showed no significant difference in the T staging category, but the N and M values were significantly higher for 18F-FAPI-04 PET/CT than for
18F-FDG PET/CT (P = 0.002 and 0.008, respectively). Thus, 14 patients were upgraded, and only 1 patient was downgraded, by 18F-FAPI-04 PET/CT compared with
18F-FDG PET/CT. A high SUVmax of the primary
tumor did not correlate with treatment response for either 18F-FAPI-04 or
18F-FDG. Conclusion: 18F-FAPI-04 PET/CT performed better than
18F-FDG PET/CT in identification of primary
tumors, LN
metastasis, and DM and in TNM staging of PDAC.