A newly developed " Flexible PET (fxPET)" is a prototype of MR-compatible mobile PET system. We tried to investigate the clinical feasibility of the fxPET with a 1.5T MRI compared with PET/CT for brain imaging. Twenty-one patients ( including 12 patients with known intracranial masses) were enrolled in this study. We compared misregistration between fxPET/MRI and PET/CT, and compared the image quality of fxPET and PET in both qualitative (visual rating) and quantitative (standardized uptake value (SUV)-based analysis ) manner. Consequently, fxPET/MRI showed acceptable misregistration and enough image quality, revealing clinical feasibility comparable to that of PET/CT.
Some previous studies1-3 using a hybrid positron emission tomography (PET)/magnetic resonance imaging (MRI) system have shown that combining the sensitive molecular imaging capability of PET with the high soft-tissue contrast of MRI has potential clinical benefits such as diagnostic accuracy. Especially for brain imaging, the role of PET/computed tomography (CT) is limited, as CT images do not show enough contrast to identify the small structures in brain. PET/MRI seems to be a preferable option due to excellent soft-tissue contrast of MRI.
However, it is not always easy to introduce such hybrid PET/MRI systems in medical facilities, due to some practical problems such as cost and space. If a mobile PET system is available, we can combine it with an existing MR unit in daily clinical settings. "Flexible PET (fxPET) is a newly developed device, which is a prototype of MR-compatible mobile PET system4, 5 (see Materials and methods).
Patients
Twenty-one patients (13 female, 8 male; age range 21-77 years; mean, 53±15 years) were enrolled in this study. Twelve patients had known intracranial lesions.
fxPET/MRI
Flexible PET (fxPET) is a dual-head mobile PET system, based on a silicon photomultiplier (SiPM)-based depth-of-interaction (DOI) time-of-flight (TOF) detector with MR compatibility (Shimadzu) (Figure 1A). Setting the fxPET in an existing MR unit, where 1.5T MR scanner (Excelart Vantage, Toshiba) was equipped, we achieved fxPET/MRI unit enabling sequential acquisition of PET and MRI images (Figure 1B).
Protocol
All subjects underwent a single-injection of 18F-fluoro-2-deoxy-D-glucose (FDG) and dual imaging (whole-body PET/CT with subsequent brain fxPET/MRI). PET/CT scans were performed based on standard clinical protocols. Subsequently, at the fxPET/MRI unit, fxPET scans were performed, followed by MRI scans.
Data processing and image analysis
PET images were reconstructed iteratively. Attenuation correction and scatter correction were performed using low-dose CT image for PET/CT, while using MRI T1-weighted image (T1WI) for fxPET/MRI.
For evaluation of misregistration6, 7 we firstly determined 6 margins (right and left, anterior and posterior, and upper and lower) of the physiologic uptake of the brain in PET and CT images. Next, we calculated the difference between the two images for each margin. Same procedures was applied to fxPET and T1WI images.
For evaluation of image quality (Figure 2), we performed visual rating and a standardized uptake value (SUV)-based analysis8, 9. As visual rating, we assessed the overall image quality of the PET image, the subjective contrast of the lesion in the PET image, and the feasibility of anatomic allocation of the PET lesion in the low-dose CT images and MRI (T1WI), related to the lesion detectability of PET/CT and fxPET/MRI. For SUV-based analysis, we firstly coregistered both PET images using the T1WI and normalized them in order to match the coordinate of the region of interest (ROI). As ROI, we selected the lesions and normal structures (bilateral caudate and vermis). Next, we measured maximum SUV (SUVmax) and mean SUV (SUVmean) within each ROI.
The average misregistration of fxPET/MRI and PET/CT was shown in Figure 3. Although the average misregistration of PET/CT was significantly smaller than that of fxPET/MRI in the left, anterior and superior margin (p<0.05), there was no significant difference between them in the right, posterior and inferior margin.
Figure 4 showed the result of visual rating. The overall PET image quality and the subjective contrast of the lesion were better in PET than in fxPET, while the feasibility of anatomic allocation of the PET lesion in MRI (T1WI) was better than that in the low-dose CT images. The numbers of lesions detected did not show significant difference between PET/CT and fxPET/MRI (14:13).
As shown in Figure 5, SUVs (SUVmax and SUVmean) showed high correlation between PET/CT and fxPET/MRI, both in lesions and normal structures.
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5. Yamakawa Y, Kobayashi T, et al. Development of a dual-head mobile DOI-TOF PET system having multi-modality compatibility. Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC), 2014 IEEE, pp. 1-3, 2014
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Figure 1. Illustration of "Flexible PET"/MRI system
(A) Flexible PET (fxPET) scanner
(B) fxPET with a 1.5T MR scanner
Figure 2. Example of fxPET/MRI and PET/CT image with suspected glioblastoma.
(Top) fxPET/MRI data: T1-weighted image (left), fusion image (center), and fxPET image (right). (Bottom) PET/CT data: low-dose CT image (left), fusion image (center), and PET image (right)