Kessler_2023_J.Nucl.Med_64_1910

Reference

Title : (68)Ga-Labeled Fibroblast Activation Protein Inhibitor ((68)Ga-FAPI) PET for Pancreatic Adenocarcinoma: Data from the (68)Ga-FAPI PET Observational Trial - Kessler_2023_J.Nucl.Med_64_1910
Author(s) : Kessler L , Hirmas N , Pabst KM , Hamacher R , Ferdinandus J , Schaarschmidt BM , Milosevic A , Nader M , Umutlu L , Uhl W , Reinacher-Schick A , Lugnier C , Witte D , Niedergethmann M , Herrmann K , Fendler WP , Siveke JT
Ref : J Nucl Med , 64 :1910 , 2023
Abstract :

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 (68)Ga-FAPI PET observational trial (NCT04571086). All of these patients underwent contrast-enhanced CT, and 38 patients additionally underwent (18)F-FDG PET. The primary study endpoint was the association of (68)Ga-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 (68)Ga-FAPI SUV(max) and histopathologic FAP expression was significant (Spearman r, 0.48; P = 0.04). For histopathology-validated lesions, (68)Ga-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 (18)F-FDG or contrast-enhanced CT, (68)Ga-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. (68)Ga-FAPI PET readers showed substantial overall agreement on the basis of the Fleiss kappa: primary kappa, 0.77 (range, 0.66-0.88). Minor and major changes in clinical management occurred in 5 patients (8.4%) after (68)Ga-FAPI PET. Conclusion: We confirmed an association of (68)Ga-FAPI PET SUV(max) and histopathologic FAP expression in pancreatic cancer patients. Additionally, we found high detection rate and diagnostic accuracy, superior to those of (18)F-FDG PET/CT. (68)Ga-FAPI might become a powerful diagnostic tool for pancreatic cancer work-up.

PubMedSearch : Kessler_2023_J.Nucl.Med_64_1910
PubMedID: 37973185

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Kessler L, Hirmas N, Pabst KM, Hamacher R, Ferdinandus J, Schaarschmidt BM, Milosevic A, Nader M, Umutlu L, Uhl W, Reinacher-Schick A, Lugnier C, Witte D, Niedergethmann M, Herrmann K, Fendler WP, Siveke JT (2023)
(68)Ga-Labeled Fibroblast Activation Protein Inhibitor ((68)Ga-FAPI) PET for Pancreatic Adenocarcinoma: Data from the (68)Ga-FAPI PET Observational Trial
J Nucl Med 64 :1910

Kessler L, Hirmas N, Pabst KM, Hamacher R, Ferdinandus J, Schaarschmidt BM, Milosevic A, Nader M, Umutlu L, Uhl W, Reinacher-Schick A, Lugnier C, Witte D, Niedergethmann M, Herrmann K, Fendler WP, Siveke JT (2023)
J Nucl Med 64 :1910