Lan_2022_Radiology_304_648

Background Gallium 68-labeled fibroblast-activation protein inhibitor ((68)Ga-FAPI), an imaging agent for detecting tumors, represents a promising alternative to fluorine 18 fluorodeoxyglucose ((18)F-FDG). Purpose To compare the potential efficacy of (68)Ga-FAPI PET/CT with that of (18)F-FDG PET/CT for detecting primary tumor and nodal and distant metastases in biliary tract cancer (BTC) and to explore the impact (tumor staging) of (68)Ga-FAPI compared with (18)F-FDG on clinical management of BTC. Materials and Methods This single-center prospective clinical study was performed at the Affiliated Hospital of Southwest Medical University between June 2020 and June 2021. Participants with BTC underwent both (68)Ga-FAPI and (18)F-FDG PET/CT. Histopathologic examination, morphologic imaging, and/or follow-up imaging served as the reference standard. The maximum standardized uptake value (SUV(max)) of the primary tumor and nodal and distant metastases between (18)F-FDG and (68)Ga-FAPI PET/CT were compared using the paired-sample t test. Results Eighteen participants with primary or recurrent BTC were evaluated (mean age, 61 years +/- 10 [SD]). The sensitivity of (68)Ga-FAPI PET/CT was higher than that of (18)F-FDG PET/CT for detecting primary tumors (16 of 16 [100%] vs 13 of 16 [81%]), nodal metastases (41 of 42 [98%] vs 35 of 42 [83%]), and distant metastases (99 of 99 [100%] vs 78 of 99 [79%]). (68)Ga-FAPI PET/CT resulted in new oncologic findings in 10 of 18 participants and upgraded tumor staging or restaging in five of 18 participants compared with (18)F-FDG PET/CT. (68)Ga-FAPI PET/CT demonstrated higher sensitivity than (18)F-FDG PET/CT in inflammatory processes secondary to tumor-related obstruction (seven of eight [88%] vs one of eight [13%]). (68)Ga-FAPI showed lower average SUV(max) in inflammatory processes than in oncologic lesions (4.9 +/- 2.6 vs 10.0 +/- 4.6, respectively; P = .003). Conclusion Gallium 68-labeled fibroblast-activation protein inhibitor PET/CT for tumor staging showed potential for more accurate staging of biliary tract cancer, thereby improving treatment decision making. Clinical trial registration no. ChiCTR2100044131 .