Fusion of [18F]FDG PET with Fluorescence Diffuse Optical Tomography to Improve Validation of Probes and Tumor Imaging

• Published in: Molecular imaging and biology Vol. 15; no. 3; pp. 316 - 325
• Main Authors: Garofalakis, Anikitos, Dubois, Albertine, Thézé, Benoît, Czarny, Bertrand, Tavitian, Bertrand, Ducongé, Frédéric
• Format: Journal Article
• Language: English
• Published: New York Springer-Verlag 01.06.2013; Springer Nature B.V; Springer Verlag
• Subjects: Animals; Cathepsins - metabolism; Cell Line, Tumor; Diffusion; Fluorescent Dyes; Fluorodeoxyglucose F18; Humans; Imaging; Life Sciences; Medicine; Medicine & Public Health; Mice; Molecular Probes; Neoplasms - diagnostic imaging; Neoplasms - metabolism; Neoplasms - pathology; Oligopeptides; Positron-Emission Tomography - methods; Radiology; Reproducibility of Results; Research Article; Tissue Distribution; Tomography, Optical - methods; Positron-emission tomography; Small-animal multimodal imaging; Fluorescence diffuse optical tomography; Fluorescence molecular tomography; Cancer; Fluorescence molecular tomography Fluorescence diffuse optical tomography Positron-emission tomography Small-animal multimodal imaging Cancer
• ISSN: 1536-1632; 1860-2002
• DOI: 10.1007/s11307-012-0581-z

Purpose Given the progress of fluorescence diffuse optical tomography (fDOT) technology, here, we study the additional benefits provided by multimodal PET/fDOT imaging by comparing the biodistribution of 2-deoxy-2-[ 18 F]fluoro- d -glucose ([ 18 F]FDG) in tumors with three fluorescent probes: a glucose analog, a protease activatable optical probe, and a ligand of αvβ3 integrin. Procedures Sequential fDOT/PET/computed tomography (CT) imaging of mice was performed with a custom multimodal mouse support that allows the subject to be transferred between the fDOT and the PET/CT scanners. Experiments were performed in xenografted tumor models derived from the human breast cancer line MDA-MB 231 and compared to ex vivo analysis. Results The three-dimensional signals showed that the fluorescent glucose analog is not colocalized with [ 18 F]FDG, raising questions about its use as a surrogate probe of the PET tracer. Fusion of [ 18 F]FDG with the other fluorescent probes showed evidence of high variability both for the protease activity and the αvβ3 integrin expression during tumor growth. Conclusion The added value of hybrid PET/fDOT over the two modalities was demonstrated for cross-validation of probes and for better characterization of tumor models.