Imaging Capabilities of the IRIS and IRIS XL-260 PET/CT Systems for High-Throughput Imaging: A Quantification Cross-Validation Study
IEEE Transactions on Radiation and Plasma Medical Sciences(2023)
摘要
The concept of imaging several subjects simultaneously is an active preclinical research topic. In this article, we assessed the imaging capabilities of two positron emission tomograph (PET)/computed tomograph (CT) systems based on similar detector technology. The IRIS system is a mice/rat imaging system arranged in two rings of eight detectors each, the more recent IRIS XL 260, dedicated to nonhuman primate (NHP) imaging has a single ring of 16 detectors. Both systems were equipped with standard animal cells (Minerve) and 3-mice adapters. Our objective is to study which of these systems could be more appropriate to perform quantitative high-throughput imaging on mice. Phantoms and [18F]FDG tumor-bearing mice acquisitions have been conducted in single- and high-throughput modes using both the IRIS (up to 3 mice) and the IRIS XL-260 PET/CT (up to 6 mice) systems. Image quality phantom results obtained in high-throughput mode show some slight degradation of the recovery coefficient for rods of 1, 2, and 3 mm in diameter compared to the single-mode results, as one would normally expect. Similarly, we observed a decrease in image uniformity between the single- and the high-throughput modes for both the IRIS PET and the IRIS XL-260 PET systems. We performed [18F]FDG tumor-bearing mice PET acquisitions with both systems. In order to estimate the quantification differences in all the studied configurations, we calculate the ratios between the %ID/g values extracted from the PET images and the ex-vivo values. In single-mode acquisitions, ratios of 0.94 ± 0.09 and 0.83 ± 0.08 were obtained for the IRIS and the IRIS XL-260 PET systems, respectively. In high-throughput mode, ratios of 0.78 ± 0.12 and 0.73 ± 0.13 were obtained for the IRIS and the IRIS XL-260 PET systems, respectively. The difference in %ID/g between static acquisitions and ex-vivo value is not statistically significant (
$p$
-value > 0.1) for both PET systems in single mode, as well as for the IRIS system in the high-throughput mode. We noted a slightly higher statistical difference between static acquisitions and ex-vivo values for the IRIS XL-260 system with a
$p$
-value of 0.015. Phantoms and in-vivo studies have made it possible to highlight the capability of the two systems to perform high-throughput acquisitions. Our results suggest that the IRIS system configuration may be the most suitable when aiming for quantitative high-throughput mice imaging. The large transverse field of view of the IRIS XL-260 makes it possible to image a greater number of mice simultaneously, which may be useful in specific cases, such as studies using an expensive radiotracer and/or with a short half-life. However, the IRIS PET/CT offers a full axial coverage of the animals and a higher sensitivity.
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关键词
Biomedical imaging,high throughput,molecular imaging,positron emission tomography (PET),system quantification
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