Impact of 68Ga-FAPI PET/CT Imaging on the Therapeutic Management of Primary and Recurrent Pancreatic Ductal Adenocarcinomas

Pancreatic ductal carcinoma (PDAC) is a highly lethal cancer, and early detection and accurate staging are critical to prolonging survival. PDAC typically has a prominent stroma including cancer-associated fibroblasts that express fibroblast activation protein (FAP). FAP is a new target molecule for...

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Veröffentlicht in:The Journal of nuclear medicine (1978) 2021-06, Vol.62 (6), p.779-786
Hauptverfasser: Roehrich, Manuel, Naumann, Patrick, Giesel, Frederik L., Choyke, Peter L., Staudinger, Fabian, Wefers, Annika, Liew, Dawn P., Kratochwil, Clemens, Rathke, Hendrik, Liermann, Jakob, Herfarth, Klaus, Jaeger, Dirk, Debus, Juergen, Haberkorn, Uwe, Lang, Matthias, Koerber, Stefan A.
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Sprache:eng
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Zusammenfassung:Pancreatic ductal carcinoma (PDAC) is a highly lethal cancer, and early detection and accurate staging are critical to prolonging survival. PDAC typically has a prominent stroma including cancer-associated fibroblasts that express fibroblast activation protein (FAP). FAP is a new target molecule for PET imaging of various tumors. In this retrospective study, we describe the clinical impact of PET/CT imaging using Ga-68-labeled FAP-inhibitors (Ga-68-FAPI PET/CT) in 19 patients with PDAC (7 primary, 12 progressive/recurrent). Methods: All patients underwent contrast-enhanced CT (ceCT) for TNM staging before Ga-68-FAPI PET/CT imaging. PET scans were acquired 60 min after administration of 150-250 MBq of Ga-68-labeled FAP-specific tracers. To characterize Ga-68-FAPI uptake over time, additional scans after 10 or 180 min were acquired in 6 patients. SUVmax and SUVmean values of PDAC manifestations and healthy organs were analyzed. The tumor burden according to Ga-68-FAPI PET/CT was compared with TNM staging based on ceCT and changes in oncologic management were recorded. Results: Compared with ceCT, Ga-68-FAPI PET/CT results led to changes in TNM staging in 10 of 19 patients. Eight of 12 patients with recurrent/progressive disease were upstaged, 1 was downstaged, and 3 had no change. In newly diagnosed PDAC, 1 of 7 patients was upstaged, and the staging of 6 patients did not change. Changes in oncologic management occurred in 7 patients. Markedly elevated uptake of Ga-68-FAPI in PDAC manifestations after 1 h was seen in most cases. Differentiation from pancreatitis based on static imaging 1 h after injection was challenging. With respect to imaging after multiple time points, PDAC and pancreatitis showed a trend for differential uptake kinetics. Conclusion: Ga-68-FAPI PET/CT led to restaging in half of the patients with PDAC and most patients with recurrent disease compared with standard of care imaging. The clinical value of Ga-68-FAPI PET/CT should be further investigated.
ISSN:0161-5505
1535-5667
DOI:10.2967/jnumed.120.253062