Lan Lianjun, Zhang Shumao, Xu Tingting, Liu Huipan, Wang Wei, Feng Yue, Wang Li, Chen Yue, Qiu Lin
From the Departments of Radiology (L.L.) and Nuclear Medicine (S.Z., T.X., H.L., W.W., Y.F., L.W., Y.C., L.Q.), The Affiliated Hospital of Southwest Medical University, No. 25 Taiping St, Jiangyang District, Luzhou 646000, People's Republic of China; Nuclear Medicine and Molecular Imaging Key Laboratory of Sichuan Province, Luzhou, People's Republic of China (L.L., S.Z., T.X., H.L., W.W., Y.F., L.W., Y.C., L.Q.); and Academician (Expert) Workstation of Sichuan Province, Luzhou, People's Republic of China (L.L., S.Z., T.X., H.L., W.W., Y.F., L.W., Y.C., L.Q.).
Radiology. 2022 Sep;304(3):648-657. doi: 10.1148/radiol.213118. Epub 2022 May 17.
Background Gallium 68-labeled fibroblast-activation protein inhibitor (Ga-FAPI), an imaging agent for detecting tumors, represents a promising alternative to fluorine 18 fluorodeoxyglucose (F-FDG). Purpose To compare the potential efficacy of Ga-FAPI PET/CT with that of 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 Ga-FAPI compared with 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 Ga-FAPI and F-FDG PET/CT. Histopathologic examination, morphologic imaging, and/or follow-up imaging served as the reference standard. The maximum standardized uptake value (SUV) of the primary tumor and nodal and distant metastases between F-FDG and Ga-FAPI PET/CT were compared using the paired-sample test. Results Eighteen participants with primary or recurrent BTC were evaluated (mean age, 61 years ± 10 [SD]). The sensitivity of Ga-FAPI PET/CT was higher than that of 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%]). 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 F-FDG PET/CT. Ga-FAPI PET/CT demonstrated higher sensitivity than F-FDG PET/CT in inflammatory processes secondary to tumor-related obstruction (seven of eight [88%] vs one of eight [13%]). Ga-FAPI showed lower average SUV in inflammatory processes than in oncologic lesions (4.9 ± 2.6 vs 10.0 ± 4.6, respectively; = .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 © RSNA, 2022 . See also the editorial by Choyke in this issue.
背景 镓68标记的成纤维细胞激活蛋白抑制剂(Ga-FAPI)是一种用于检测肿瘤的显像剂,是氟18氟脱氧葡萄糖(F-FDG)的一种有前景的替代物。目的 比较Ga-FAPI PET/CT与F-FDG PET/CT在检测胆管癌(BTC)原发肿瘤、区域淋巴结转移和远处转移方面的潜在效能,并探讨与F-FDG相比,Ga-FAPI对BTC临床管理的影响(肿瘤分期)。材料与方法 本单中心前瞻性临床研究于2020年6月至2021年6月在西南医科大学附属医院进行。BTC患者同时接受了Ga-FAPI和F-FDG PET/CT检查。组织病理学检查、形态学成像和/或随访成像作为参考标准。采用配对样本t检验比较F-FDG和Ga-FAPI PET/CT之间原发肿瘤、区域淋巴结转移和远处转移的最大标准化摄取值(SUV)。结果 对18例原发性或复发性BTC患者进行了评估(平均年龄61岁±10[标准差])。在检测原发肿瘤(16例中的16例[100%]对16例中的13例[81%])、区域淋巴结转移(42例中的41例[98%]对42例中的35例[83%])和远处转移(99例中的99例[100%]对99例中的78例[79%])方面,Ga-FAPI PET/CT的敏感性高于F-FDG PET/CT。与F-FDG PET/CT相比,Ga-FAPI PET/CT使18例患者中的10例有了新的肿瘤学发现,并使18例患者中的5例肿瘤分期得到升级或重新分期。在肿瘤相关梗阻继发的炎症过程中,Ga-FAPI PET/CT的敏感性高于F-FDG PET/CT(8例中的7例[88%]对8例中的1例[13%])。Ga-FAPI在炎症过程中的平均SUV低于肿瘤性病变(分别为4.9±2.6和10.0±4.6;P = .003)。结论 镓68标记的成纤维细胞激活蛋白抑制剂PET/CT用于肿瘤分期显示出对胆管癌进行更准确分期的潜力,从而改善治疗决策。临床试验注册号:ChiCTR2100044131 © RSNA, 2022 。另见本期Choyke的社论。