11–14 May 2026
Valencia Hotel Las Arenas
Europe/Zurich timezone

First Results from the SAVANT Ultra-High-Resolution Phoswich-Based DOI Brain PET Scanner

13 May 2026, 11:10
20m
Valencia Hotel Las Arenas

Valencia Hotel Las Arenas

C/ d'Eugènia Viñes, 22, 24, Poblados Marítimos, 46011 Valencia, Spain

Speaker

Prof. Roger Lecomte (Université de Sherbrooke, Sherbrooke Molecular Imaging Center of CRCHUS, IR&T Inc.)

Description

High spatial resolution is essential to successfully resolve small structures in the brain and to enable imaging of neurological pathways at the onset of diseases. A key challenge with ultra-high-resolution PET scanners is the significant degradation of resolution that occurs beyond the central area of the field-of-view (FOV). The Ultra-High-Resolution (UHR) Brain PET scanner was designed with short (12 mm) LYSO crystals to mitigate the parallax error off the FOV center, but at the expense of reduced sensitivity [1]. To address these limitations, the LabPET II based technology platform of the UHR was upgraded to implement depth-of-interaction (DOI) measurement using longer (15 mm) dual LGSO phoswich detectors in the Scanner Approaching in Vivo Autoradiographic Neuro Tomography (SAVANT). Simulation results indicate an estimated gain in sensitivity of 40%, while maintaining the resolution below 2 mm FWHM at the edge of the brain. For DOI determination, the crystal identification between slow (43-48 ns decay time) and fast (30-35 ns decay time) LGSO scintillators uses a model-based dual-threshold time-over-threshold (ToT) discrimination technique that is currently achieving better than 70% accuracy. The 6.5/8.5 mm length ratio of the top slow and bottom fast LGSO scintillators resulted from trade-offs between off-center spatial resolution degradation and balanced coincidence detection efficiency of the two crystal layers. We report the first experimental results obtained using the partially assembled scanner (182 mm axial extent), which demonstrate the improvement in resolution uniformity across the radial FOV achieved using this simple DOI discrimination scheme. Point source and phantom measurements taken at various radial positions within the FOV effectively demonstrate the gain in spatial resolution compared to non-DOI measurements, though not reaching the resolution predicted by simulation. It is anticipated that further refinement of the crystal identification process, potentially using AI, will yield the forecasted benefits from simulation. Preliminary results for imaging the human brain will be presented.

[1] E. Gaudin, M. Toussaint, C. Thibaudeau, M. Paille, R. Fontaine, and R. Lecomte, “Performance Simulation of an Ultrahigh Resolution Brain PET Scanner Using 1.2-mm Pixel Detectors,” IEEE Trans. Radiat. Plasma Med. Sci., vol. 3, no. 3, pp. 334–342, May 2019, doi: 10.1109/TRPMS.2018.2877511.

Track PSMR
Presentation type Oral

Author

Prof. Roger Lecomte (Université de Sherbrooke, Sherbrooke Molecular Imaging Center of CRCHUS, IR&T Inc.)

Co-authors

Arnaud Samson (Université de Sherbrooke) Christian Thibaudeau (IR&T Inc.) Georges El Fakhri (Yale University School of Medicine,) Jean-Baptiste Michaud (Université de Sherbrooke) Jean-François Beaudoin (Sherbrooke Molecular Imaging Center of CRCHUS) Jonathan Bouchard (Université de Sherbrooke) Marc-André Tétrault (Université de Sherbrooke) Maxime Gaudreault (Université de Sherbrooke) Maxime Toussaint (Nantes Université Laboratoire CRCI2NA, INSERM) Nicolas Viscogliosi (Université de Sherbrooke) Otman Sarrhini (Sherbrooke Molecular Imaging Center of CRCHUS) Romain Espagnet (Université de Sherbrooke) Réjean Fontaine (Université de Sherbrooke) Thibault Marin (Yale University School of Medicine,) Tommy Galarneau (Sherbrooke Molecular Imaging Center of CRCHUS) Yanis Chemli (Yale University School of Medicine,) Yassir Najmaoui (Université de Sherbrooke, Yale University School of Medicine,) Éric Lavallée (Sherbrooke Molecular Imaging Center of CRCHUS) Étienne Croteau (Sherbrooke Molecular Imaging Center of CRCHUS)

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