68Ga-Labeled Fibroblast Activation Protein Inhibitor (68Ga-FAPI) PET for Pancreatic Adenocarcinoma: Data from the 68Ga-FAPI PET Observational Trial

被引:10
|
作者
Kessler, Lukas [1 ,2 ,3 ,4 ]
Hirmas, Nader [1 ,3 ,4 ]
Pabst, Kim M. [1 ,2 ]
Hamacher, Rainer [3 ,4 ,5 ]
Ferdinandus, Justin [1 ,2 ]
Schaarschmidt, Benedikt M. [2 ,3 ]
Milosevic, Aleksandar [2 ,3 ,4 ]
Nader, Michael [1 ]
Umutlu, Lale [2 ,3 ,4 ]
Uhl, Waldemar [6 ]
Reinacher-Schick, Anke [7 ]
Lugnier, Celine [6 ]
Witte, David [8 ]
Niedergethmann, Marco [8 ]
Herrmann, Ken [1 ,3 ,4 ]
Fendler, Wolfgang P. [1 ,3 ,4 ]
Siveke, Jens T. [3 ,4 ,9 ,10 ,11 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, Dept Nucl Med, Essen, Germany
[2] Univ Hosp Essen, Dept Diagnost & Intervent Radiol & Neuroradiol, Essen, Germany
[3] Univ Hosp Essen, German Canc Consortium DKTK, Partner Site, Essen, Germany
[4] German Canc Res Ctr, Essen, Germany
[5] Univ Duisburg Essen, West German Canc Ctr, Dept Med Oncol, Essen, Germany
[6] Ruhr Univ Bochum, St Josef Hosp Bochum, Dept Gen & Visceral Surg, Bochum, Germany
[7] Ruhr Univ Bochum, St Josef Hosp, Dept Hematol & Oncol Palliat Care, Bochum, Germany
[8] Alfried Krupp Hosp, Dept Gen & Visceral Surg, Essen, Germany
[9] Univ Duisburg Essen, Univ Hosp Essen, Bridge Inst Expt Tumor Therapy, West German Canc Ctr, Essen, Germany
[10] Univ Hosp Essen, Div Solid Tumor Translat Oncol, German Canc Consortium DKTK, Partner Site, Heidelberg, Germany
[11] German Canc Res Ctr, Heidelberg, Germany
关键词
pancreatic ductal adenocarcinoma; PDAC; cancer imag-ing; 68Ga-FAPI; fibroblast activation protein; PET; CARCINOMA; DIAGNOSIS;
D O I
10.2967/jnumed.122.264827
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The fibroblast activation protein (FAP) is highly expressed on carcinoma-associated fibroblasts in the stroma of pancreatic cancer and thus is a promising target for imaging and therapy. Preliminary data on PET imaging with radiolabeled FAP inhibitors (FAPIs) demonstrate superior tumor detection. Here we assess the accuracy of FAP-directed PET in patients with pancreatic cancer. Methods: Of 64 patients with suspected or proven pancreatic cancer, 62 (97%) were included in the data analysis of the 68Ga-FAPI PET observational trial (NCT04571086). 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. Results: The primary endpoint was met: The association between 68Ga-FAPI SUVmax and histopathologic FAP expression was significant (Spearman r, 0.48; P 5 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 K: primary K, 0.77 (range, 0.66-0.88). Minor and major changes in clinical management occurred in 5 patients (8.4%) after 68Ga-FAPI PET. Conclusion: We confirmed an association of 68Ga-FAPI PET SUVmaxand 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 diag-nostic tool for pancreatic cancer work-up.
引用
收藏
页码:1910 / 1917
页数:8
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