Pancreatic ductal adenocarcinoma (PDAC) is a deadly cancer with extremely poor survival rates. It is well known that because of late detection, PDAC is often diagnosed in advanced or metastasized stages, which emphasizes the necessity of accurate imaging methods for suspected lesions.
The fibroblast activation protein (FAP) is highly expressed on carcinoma-associated fibroblasts in the stroma of pancreatic cancer and thus is promising target for imaging and therapy. Preliminary data on PET imaging with radiolabeled FAP inhibitors (FAPIs) demonstrate superior tumor detection.
A recent study in The Journal of Nuclear Medicine assessed the accuracy of FAP-directed PET in patients with pancreatic cancer. The study confirmed an association of 68Ga-FAPI PET SUV max and histopathologic FAP expression in pancreatic cancer patients. Additionally, there was high detection rate and diagnostic accuracy, superior to those of 18F-FDG PET/CT. 68Ga-FAPI might become a powerful diagnostic tool for pancreatic cancer work-up.
The researchers included 64 patients with suspected or proven pancreatic cancer, 62 (97%) were included in the data analysis of the 68Ga-FAPI PET observational trial. All of these patients underwent contrast-enhanced CT, and 38 patients additionally underwent 18F-FDG PET. The primary study endpoint was the association of 68Ga-FAPI PET uptake intensity and histopathologic FAP expression. Secondary endpoints were detection rate, diagnostic performance, interreader reproducibility, and change in management. Datasets were interpreted by 2 masked readers.
The key points of the study are
• The primary endpoint was met: The association between 68Ga-FAPI SUVmax and histopathologic FAP expression was significant (Spearman r, 0.48; P = 0.04).
• For histopathology-validated lesions, 68Ga-FAPI PET showed high sensitivity and positive predictive values (PPVs) on per-patient (sensitivity, 100%; PPV, 96.3%) and per-region (sensitivity, 100%; PPV, 97.0%) bases.
• In a head-to-head comparison versus 18F-FDG or contrast-enhanced CT, 68Ga-FAPI detected more tumor on a per-lesion (84.7% vs. 46.5% vs. 52.9%), per-patient (97.4% vs. 73.7% vs. 92.1%), or per-region (32.6% vs. 18.8% vs. 23.7%) basis, respectively.
• 68Ga-FAPI PET readers showed substantial overall agreement on the basis of the Fleiss κ: primary κ, 0.77 (range, 0.66–0.88).
• Minor and major changes in clinical management occurred in 5 patients (8.4%) after 68Ga-FAPI PET.
Researchers concluded that “We confirmed an association of 68Ga-FAPI PET SUV max and histopathologic FAP expression in pancreatic cancer patients. Additionally, we found high detection rate and diagnostic accuracy, superior to those of 18F-FDG PET/CT. 68Ga-FAPI might become a powerful diagnostic tool for pancreatic cancer work-up.”
Reference: Lukas Kessler Nader Hirmas, KimM.Pabst et al; 68Ga-Labeled Fibroblast Activation Protein Inhibitor (68Ga-FAPI)PET for Pancreatic Adenocarcinoma: Data from the 68Ga-FAPIPET Observational Trial; Journal of Nuclear Medicine, published on November 16, 2023 as doi:10.2967/jnumed.122.264827
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