PET/CT With 68Ga-FAPI Detects More Biliary Tract Cancer than 18F-FDG
Gallium 68–labeled fibroblast-activation protein inhibitor (68Ga-FAPI) PET/CT showed potential to more accurately stage biliary tract cancer than Fluorine 18 fluorodeoxyglucose (18F-FDG) PET/CT in a study published in Radiology.
The single-center prospective clinical study was performed at the Affiliated Hospital of Southwest Medical University between June 2020 and June 2021. Eighteen patients with primary or recurrent biliary tract cancer underwent both 68Ga-FAPI and 18F-FDG PET/CT. Using the paired-sample t test, the maximum standardized uptake value (SUVmax) of the primary tumor and nodal and distant metastases between 18F-FDG and 68Ga-FAPI PET/CT were compared.
The sensitivity of 68Ga-FAPI PET/CT was higher than 18F-FDG PET/CT in primary tumors (100% versus 81%), nodal metastases (98% vs 83%), and distant metastases (100% vs 79%). With 68Ga-FAPI, 10 participants had new oncologic findings and five had upgraded tumor staging or restaging. In inflammatory processes secondary to tumor-related obstruction, 68Ga-FAPI PET/CT demonstrated higher sensitivity than 18F-FDG PET/CT (88% vs 13%).
Two experienced nuclear medicine physicians, both of whom had more than 10 years of experience in nuclear oncology, evaluated both the 68Ga-FAPI PET/CT and 18F-FDG PET/CT studies in random order.
68Ga-FAPI PET/CT visualized 99 distant metastases in 12 participants while 18F-FDG PET/CT missed 21 distant metastatic lesions in seven participants. 65 of the 99 distant metastases were localized in the liver. Also, 68Ga-FAPI PET/CT demonstrated a higher detection efficacy for metastatic lymph nodes compared with 18F-FDG PET/CT.
The authors conclude that 68Ga-FAPI PET/CT is superior to 18F-FDG PET/CT for detecting the primary tumor and nodal and distant metastases in participants with biliary tract cancer. In addition to upgrade staging or restaging five patients, 68Ga-FAPI PET/CT showed good detection efficacy for inflammatory and reactive processes secondary to tumor-related obstruction of the proximal bile and/or pancreatic duct.
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