Prostate-Specific Membrane Antigen Targeted Pet/CT Imaging in Patients with Colon, Gastric and Pancreatic Cancer

Floris A. Vuijk*, Fleur Kleiburg, Wyanne A. Noortman, Linda Heijmen, Shirin Feshtali Shahbazi, Floris H.P. van Velden, Victor M. Baart, Shadhvi S. Bhairosingh, Bert D. Windhorst, Lukas J.A.C. Hawinkels, Petra Dibbets-Schneider, Neanke Bouwman, Stijn A.L.P. Crobach, Arantza Fariña-Sarasqueta, Andreas W.K.S. Marinelli, Daniela E. Oprea-Lager, Rutger Jan Swijnenburg, Frits Smit, Alexander L. Vahrmeijer, Lioe Fee de Geus-OeiDenise E. Hilling, Marije Slingerland

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

6 Citations (Scopus)
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Current imaging modalities frequently misjudge disease stage in colorectal, gastric and pancreatic cancer. As treatment decisions are dependent on disease stage, incorrect staging has serious consequences. Previous preclinical research and case reports indicate that prostate-specific membrane antigen (PSMA)-targeted PET/CT imaging might provide a solution to some of these challenges. This prospective clinical study aims to assess the feasibility of [18F]DCFPyL PET/CT imaging to target and visualize primary colon, gastric and pancreatic cancer. In this prospective clinical trial, patients with colon, gastric and pancreatic cancer were included and underwent both [18F]DCFPyL and [18F]FDG PET/CT scans prior to surgical resection or (for gastric cancer) neoadjuvant therapy. Semiquantitative analysis of immunohistochemical PSMA staining was performed on the surgical resection specimens, and the results were correlated to imaging parameters. The results of this study demonstrate detection of the primary tumor by [18F]DCFPyL PET/CT in 7 out of 10 patients with colon, gastric and pancreatic cancer, with a mean tumor-to-blood pool ratio (TBR) of 3.3 and mean SUVmax of 3.6. However, due to the high surrounding uptake, visual distinction of these tumors was difficult, and the SUVmax and TBR on [18F]FDG PET/CT were significantly higher than on [18F]DCFPyL PET/CT. In addition, no correlation between PSMA expression in the resection specimen and SUVmax on [18F]DCFPyL PET/CT was found. In conclusion, the detection of several gastrointestinal cancers using [18F]DCFPyL PET/CT is feasible. However, low tumor expression and high uptake physiologically in organs/background hamper the clear distinction of the tumor. As a result, [18F]FDG PET/CT was superior in detecting colon, gastric and pancreatic cancers.

Original languageEnglish
Article number6209
Issue number24
Publication statusPublished - 15 Dec 2022

Bibliographical note

Funding Information:
This study was financially supported by the Leiden University Fund (No. W19302-2-62, dr. M. Slingerland), the Dutch Cancer Society (KWF) Bas Mulder Award (No. UL 2015-7966, dr. D.E. Hilling), the KWF Young Investigators Grant (No. 11289, dr. R.J. Swijnenburg) and a European Research Council (ERC) Advanced Grant (no. 323105).

Publisher Copyright: © 2022 by the authors.


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