Motion-resolved parametric imaging derived from short dynamic [<sup>18</sup>F]FDG PET/CT scans.

Authors

Artesani A,van Sluis J,Providência L,van Snick JH,Slart RHJA,Noordzij W,Tsoumpas C

Affiliations (3)

  • Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, Groningen 9713 GZ, Netherlands; Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, 20072 Pieve Emanuele, Milan, Italy; IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089 Rozzano, Milan, Italy. Electronic address: [email protected].
  • Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, Groningen 9713 GZ, Netherlands.
  • Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Hanzeplein 1, Groningen 9713 GZ, Netherlands; Biomedical Photonic Imaging Group, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.

Abstract

This study aims to assess the added value of utilizing short-dynamic whole-body PET/CT scans and implementing motion correction before quantifying metabolic rate, offering more insights into physiological processes. While this approach may not be commonly adopted, addressing motion effects is crucial due to their demonstrated potential to cause significant errors in parametric imaging. A 15-minute dynamic FDG PET acquisition protocol was utilized for four lymphoma patients undergoing therapy evaluation. Parametric imaging was obtained using a population-based input function (PBIF) derived from twelve patients with full 65-minute dynamic FDG PET acquisition. AI-based registration methods were employed to correct misalignments between both PET and ACCT and PET-to-PET. Tumour characteristics were assessed using both parametric images and standardized uptake values (SUV). The motion correction process significantly reduced mismatches between images without significantly altering voxel intensity values, except for SUV<sub>max</sub>. Following the alignment of the attenuation correction map with the PET frame, an increase in SUV<sub>max</sub> in FDG-avid lymph nodes was observed, indicating its susceptibility to spatial misalignments. In contrast, Patlak K<sub>i</sub> parameter was highly sensitive to misalignment across PET frames, that notably altered the Patlak slope. Upon completion of the motion correction process, the parametric representation revealed heterogeneous behaviour among lymph nodes compared to SUV images. Notably, reduced volume of elevated metabolic rate was determined in the mediastinal lymph nodes in contrast with an SUV of 5 g/ml, indicating potential perfusion or inflammation. Motion resolved short-dynamic PET can enhance the utility and reliability of parametric imaging, an aspect often overlooked in commercial software.

Topics

Journal Article

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