ORIGINAL ARTICLE   

The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2023 March;67(1):57-68

DOI: 10.23736/S1824-4785.21.03300-8

Copyright © 2021 EDIZIONI MINERVA MEDICA

language: English

Reduction of emission time for [68Ga]Ga-PSMA PET/CT using the digital biograph vision: a phantom study

Pedro FRAGOSO COSTA ¹ ✉, Walter JENTZEN ¹, Finja SÜßELBECK ¹, Wolfgang P. FENDLER ¹, Christoph RISCHPLER ¹, Ken HERRMANN ¹, Maurizio CONTI ², David KERSTING ¹, Manuel WEBER ¹

¹ Department of Nuclear Medicine, Essen University Hospital, Duisburg-Essen University, Essen, Germany; ² Siemens Medical Solutions USA, Inc., Knoxville, TN, USA

BACKGROUND: The aim of this phantom study was to optimize the [⁶⁸Ga]Ga-PSMA PET/CT examination in terms of scan time duration and image reconstruction parameters, in combination with PSF and TOF modelling, in a digital Biograph Vision PET/CT scanner.
METHODS: Three types of phantoms were used: 1) soft-tissue tumor phantom consisting of six spheres mounted in a torso phantom; 2) bone-lung tumor phantom; 3) resolution phantom. Phantom inserts were filled with activity concentrations (ACs) that were derived from clinical data. Phantom data were acquired in list-mode at one bed position. Images with emission data ranging from 30 to 210 s in 30-s increments were reconstructed from a reference image acquired with 3.5-min emission. Iterative image reconstruction (OSEM), point-spread-function (PSF) and time-of-flight (TOF) options were applied using different iterations, Gaussian filters, and voxel sizes. The criteria for image quality was lesion detectability and lesion quantification, evaluated as contrast-to-noise ratio (CNR) and maximum AC (peak AC), respectively. A threshold value of CNR above 6 and percentage maximum AC (peak AC) deviation range of ±20% of the reference image were considered acceptable. The proposed single-bed scan time reduction was projected to a whole-body examination (patient validation scan) using the continuous-bed-motion mode.
RESULTS: Sphere and background ACs of 20 kBq/mL and 1 kBq/mL were selected, respectively. The optimized single-bed scan time was approximately 60 s using OSEM-TOF or OSEM-TOF+PSF (four iterations, 4.0-mm Gaussian filter and almost isotropic voxel size of 3.0-mm side length), resulting in a PET spatial resolution of 6.3 mm for OSEM-TOF and 5.5 mm for OSEM-TOF+PSF. In the patient validation, the maximum percentage difference in lesion quantification between standard and optimized protocol (whole-body scan time of 15 vs. 5 min) was below 19%.
CONCLUSIONS: A reduction of single-bed and whole-body scan time for [⁶⁸Ga]Ga-PSMA PET/CT compared to current recommended clinical acquisition protocols is postulated. Clinical studies are warranted to validate the applicability of this protocol.

KEY WORDS: Positron-emission tomography; Glu-NH-CO-NH-Lys-(Ahx)-((68)Ga(HBED-CC)); Radiopharmaceuticals; Molecular imaging