Hirmas Nader, Hamacher Rainer, Sraieb Miriam, Ingenwerth Marc, Kessler Lukas, Pabst Kim M, Barbato Francesco, Lueckerath Katharina, Kasper Stefan, Nader Michael, Schildhaus Hans-Ulrich, Kesch Claudia, von Tresckow Bastian, Hanoun Christine, Hautzel Hubertus, Aigner Clemens, Glas Martin, Stuschke Martin, Kümmel Sherko, Harter Philipp, Lugnier Celine, Uhl Waldemar, Niedergethmann Marco, Hadaschik Boris, Grünwald Viktor, Siveke Jens T, Herrmann Ken, Fendler Wolfgang P
Department of Nuclear Medicine, University of Duisburg-Essen, and German Cancer Consortium (DKTK)-University Hospital Essen, Essen, Germany.
Department of Medical Oncology, West German Cancer Center, University of Duisburg-Essen, and DKTK-University Hospital Essen, Essen, Germany.
J Nucl Med. 2023 May;64(5):711-716. doi: 10.2967/jnumed.122.264689. Epub 2022 Dec 29.
We present an overview of our prospective fibroblast-activation protein inhibitor (FAPI) registry study across a 3-y period, with head-to-head comparison of tumor uptake in Ga-FAPI and F-FDG PET, as well as FAP immunohistochemistry. This is an interim analysis of the ongoing Ga-FAPI PET prospective observational trial at our department. Patients who underwent clinical imaging with Ga-FAPI PET between October 2018 and October 2021 were included. Tracer uptake was quantified by SUV for tumor lesions and by SUV for normal organs. PET tumor volume (40% isocontour) and tumor-to-background ratios were calculated. Correlation between SUV and FAP staining in tissue samples was analyzed. In total, 324 patients with 21 different tumor entities underwent Ga-FAPI imaging; 237 patients additionally received F-FDG PET. The most common tumor entities were sarcoma (131/324, 40%), pancreatic cancer (67/324, 21%), and primary tumors of the brain (22/324, 7%). The mean primary tumor SUV was significantly higher for Ga-FAPI than F-FDG among pancreatic cancer (13.2 vs. 6.1, < 0.001) and sarcoma (14.3 vs. 9.4, < 0.001), and the same was true for mean SUV in metastatic lesions of pancreatic cancer (9.4 vs. 5.5, < 0.001). Mean primary tumor maximum tumor-to-background ratio was significantly higher for Ga-FAPI than F-FDG across several tumor entities, most prominently pancreatic cancer (14.7 vs. 3.0, < 0.001) and sarcoma (17.3 vs. 4.7, < 0.001). Compared with F-FDG, Ga-FAPI showed superior detection for locoregional disease in sarcoma (52 vs. 48 total regions detected) and for distant metastatic disease in both sarcoma (137 vs. 131) and pancreatic cancer (65 vs. 57), respectively. Among 61 histopathology samples, there was a positive correlation between Ga-FAPI SUV and overall FAP immunohistochemistry score ( = 0.352, = 0.005). Ga-FAPI demonstrates higher absolute uptake in pancreatic cancer and sarcoma, as well as higher tumor-to-background uptake along with improved tumor detection for pancreatic cancer, sarcoma, and other tumor entities when compared with F-FDG. Ga-FAPI is a new tool for tumor staging with theranostic potential.
我们展示了一项为期3年的前瞻性成纤维细胞激活蛋白抑制剂(FAPI)注册研究的概述,对镓标记的FAPI和氟代脱氧葡萄糖(F-FDG)PET中的肿瘤摄取以及FAP免疫组织化学进行了直接比较。这是我们科室正在进行的镓标记FAPI PET前瞻性观察性试验的中期分析。纳入了2018年10月至2021年10月期间接受镓标记FAPI PET临床成像的患者。通过标准化摄取值(SUV)对肿瘤病变和正常器官的示踪剂摄取进行定量。计算PET肿瘤体积(40%等剂量线)和肿瘤与背景比值。分析组织样本中SUV与FAP染色之间的相关性。共有324例患有21种不同肿瘤实体的患者接受了镓标记FAPI成像;237例患者还接受了F-FDG PET检查。最常见的肿瘤实体是肉瘤(131/324,40%)、胰腺癌(67/324,21%)和脑原发性肿瘤(22/324,7%)。在胰腺癌(13.2对6.1,<0.001)和肉瘤(14.3对9.4,<0.001)中,镓标记FAPI的原发性肿瘤平均SUV显著高于F-FDG,胰腺癌转移灶的平均SUV也是如此(9.4对5.5,<0.001)。在多个肿瘤实体中,镓标记FAPI的原发性肿瘤平均最大肿瘤与背景比值显著高于F-FDG,最显著的是胰腺癌(14.7对3.0,<0.001)和肉瘤(17.3对4.7,<0.001)。与F-FDG相比,镓标记FAPI在肉瘤的局部疾病检测方面表现更优(分别检测到52个和48个区域),在肉瘤(137对131)和胰腺癌(65对57)的远处转移疾病检测方面也更优。在61份组织病理学样本中,镓标记FAPI SUV与总体FAP免疫组织化学评分之间存在正相关(r = 0.352,P =