Papers
Topics
Authors
Recent
Search
2000 character limit reached

Investigating heterogeneous PSMA ligand uptake inside parotid glands

Published 4 Jan 2024 in physics.med-ph | (2401.02496v1)

Abstract: The purpose was to investigate the spatial heterogeneity of prostate-specific membrane antigen (PSMA) positron emission tomography (PET) uptake within parotid glands. We aim to quantify patterns in well-defined regions to facilitate further investigations. Furthermore, we investigate whether uptake is correlated with computed tomography (CT) texture features. Parotid glands from [18F]DCFPyL PSMA PET/CT images of 30 prostate cancer patients were analyzed. Thresholding was used to define high-uptake regions, and uptake statistics were computed within various divisions. Spearman's rank correlation coefficient was calculated between PSMA PET uptake and the Grey Level Run Length Matrix (GLRLM) using a long and short run length emphasis (GLRLML and GLRLMS) in subregions of parotid glands. PSMA PET uptake was significantly higher (p < 0.001) in lateral/posterior regions of the glands than anterior/medial regions. Maximum uptake was found in the lateral half of parotid glands in 50 out of 60 glands. The difference in SUV between parotid halves is greatest when parotids are divided by a plane separating the anterior/medial and posterior/lateral halves symmetrically. PSMA PET uptake was significantly correlated with CT GLRLML (p < 0.001), and anti-correlated with CT GLRLMS (p < 0.001). Uptake of PSMA PET is heterogeneous within parotid glands, with uptake biased towards lateral and posterior regions. Uptake patterns within parotid glands were found to be strongly correlated with CT texture features, suggesting the possible future use of CT texture features as a proxy for inferring PSMA PET uptake in salivary glands.

Summary

No one has generated a summary of this paper yet.

Paper to Video (Beta)

No one has generated a video about this paper yet.

Whiteboard

No one has generated a whiteboard explanation for this paper yet.

Continue Learning

We haven't generated follow-up questions for this paper yet.

Collections

Sign up for free to add this paper to one or more collections.