Modelling image quality over extended [18F]FDG uptake times for low-dose positron emission mammography
Elliott De Benetti1, Tobias Preckel2, Apichart Linhananta1
1Department of Physics, Lakehead University, Thunder Bay, ON, Canada.
Introduction:
This study investigated the effect of [18F]fluorodeoxyglucose ([18F]FDG) uptake time on image quality in low-dose positron emission mammography (PEM) using kinetic modelling.
Methods:
Fifteen malignant lesions from thirteen women newly diagnosed with breast cancer were imaged using low-dose [18F]FDG PEM. Tumour and normal breast tissue time-activity curves (TACs) were generated using a population-based arterial input function (AIF) and a two-tissue compartmental model. Modelling was performed at [18F]FDG doses of 1, 2, 5, and 10 mCi (37, 74, 185, and 370 MBq), and image quality was assessed using contrast-to-noise ratio (CNR) over a 6-hour uptake period.
Results:
Extending uptake times beyond the 1-hour clinical standard significantly improved CNR across all doses, with comparable proportional gains. Relative to 1 hour post-injection, CNR increased by approximately 30% at 1.5 hours, 53% at 2 hours, and 77% at 3 hours, although uncertainty widened at 3 hours and beyond, particularly at the lowest dose (1 mCi). Relatively small variations in uptake time were also found to produce substantial changes in the standardized uptake value (SUV).
Discussion:
These findings demonstrate that extending uptake times by even 30 minutes beyond the 1-hour clinical standard may significantly enhance image CNR for low-dose [18F]FDG PEM. The sensitivity of SUV to small variations in uptake time supports the need to closely match uptake time between baseline and follow-up scans in treatment response assessment. Overall, these modelling results encourage further clinical research into optimizing uptake time protocols, which may help support the broader adoption of low-dose PEM in future work.
Clinical Trials Registration:
https://clinicaltrials.gov/study/NCT03520218, identifier NCT03520218.
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