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ORIGINAL ARTICLE
The Quarterly Journal of Nuclear Medicine and Molecular Imaging 2021 December;65(4):386-95
DOI: 10.23736/S1824-4785.17.02790-X
Copyright © 2015 EDIZIONI MINERVA MEDICA
language: English
Evaluation and clinical quantification of neoplastic lesions and physiological structures in TOF- versus non-TOF-PET/MRI: a pilot study
Felipe de GALIZA BARBOSA 1 ✉, Gaspar DELSO 2, Konstantinos G. ZEIMPEKIS 1, 3, Edwin E. ter VOERT 1, Martin HÜLLNER 1, 4, Paul STOLZMANN 1, 4, Patrick VEIT‑HAIBACH 1, 5
1 Division of Nuclear Medicine, Department of Medical Imaging, Zurich University Hospital, Zurich, Switzerland; 2 GE Healthcare, Waukesha, WI, USA; 3 Department of Information Technology and Electrical Engineering, Swiss Federal Institute of Technology in Zurich (ETHZ), Zurich, Switzerland; 4 Division of Neuroradiology, Department of Medical Imaging, Zurich University Hospital, Zurich, Switzerland; 5 Department of Medical, Diagnostic and Interventional Radiology, Zurich University Hospital, Zurich, Switzerland
BACKGROUND: The aim of this study was to clinically assess a new PET/MRI technology in which the PET-component features a new PET detector and time-of-flight (TOF) technology. Thus, a comparison was made of SUVmax/SUVmean of neoplastic lesions and physiological structures between TOF- and non-TOF-PET/MRI imaging. Image quality derived from TOF-PET/MRI, non-TOF-PET/MRI reconstruction, and FDG-PET/CT was qualitatively evaluated. Lastly, we did clinical measurements to evaluate the PET- detector sensitivity in order to better understand the background of our clinical results.
METHODS: Twenty-seven oncological patients were prospectively enrolled and evaluated with FDG-PET/CT and PET/MRI (15 males, 12 females; mean age 56±10 years). Time between injection and PET/CT was 62.4 ±7.6 min, consecutive start of imaging of PET/MRI was 104.6±18.2 minutes after injection. To assess the differences between TOF and non-TOF, all PET-images of the PET/MRI were reconstructed twice - with and without TOF. To compare lesion and tissue characterization between both reconstructions, malignant lesions as well as physiological structures were compared. Furthermore, PET image quality, artifacts, image sharpness, noise and lesion detectability were assessed as well. Count rates between both systems were also compared.
RESULTS: All malignant lesions and the majority of physiologic tissue (except the subcutaneous fat, spleen and blood pool) showed a good correlation concerning SUV (max and mean) measurements between PET/CT, non-TOF and TOF reconstructions. The general image quality was rated statistically significant superior in non-TOF (P<0.001) and TOF reconstruction in PET/MRI (P<0.01) compared to PET/CT. Furthermore, TOF-PET/MRI was rated superior concerning image quality (P<0.05) compared to non-TOF-PET/MRI. The ratio of emitted/received events between both systems (PET/CT and PET/MRI) was 2.78.
CONCLUSIONS: PET/MRI with TOF is reliable concerning SUV quantification and image quality. The technical promise of an improved sensitivity of the new PET detector in this PET/MRI device could be confirmed in a clinical setting.
KEY WORDS: Multimodal imaging; Positron-emission tomography; Magnetic resonance imaging; Neoplasms