Abstract:This paper addresses 123I and 125I dual isotope SPECT imaging, which can be challenging because of spectrum overlap in the low energy spectrums of these isotopes. We first quantify the contribution of low-energy photons from each isotope using GATE-based Monte Carlo simulations for the MOBY mouse phantom. We then describe and analyze a simple, but effective method that uses the ratio of detected low and high energy 123I activity to separate the mixed low energy 123I and 125I activities. Performance is compared… Show more
“…Our study is unique as there have been no other simulation studies, to the best of our knowledge, performing SPECT imaging of 177 Lu and 90 Y combined. Dual-isotope SPECT imaging based on Monte Carlo simulations have been performed for radioisotope pairs such as 99m Tc/ 123 I [35] 123 I/ 125 I [36], and combinations of 99m Tc, 111 In, 123 I, 177 Lu, and 201 Tl [37], but not 177 Lu and 90 Y. Dosimetry simulations of 177 Lu and 90 Y therapy have been performed [38,39] which highlights the importance of a study such as ours; dosimetry is impractical outside of a simulation if imaging cannot be performed quantitatively. Imaging has been performed in dual-isotope PRRT with 177 Lu and 90 Y [40], but dosimetry was not performed.…”
This work aims to investigate the accuracy of quantitative SPECT imaging of 177Lu in the presence of 90Y, which occurs in dual-isotope radiopharmaceutical therapy (RPT) involving both isotopes. We used the GATE Monte Carlo simulation toolkit to conduct a phantom study, simulating spheres filled with 177Lu and 90Y placed in a cylindrical water phantom that was also filled with activity of both radionuclides. We simulated multiple phantom configurations and activity combinations by varying the location of the spheres, the concentrations of 177Lu and 90Y in the spheres, and the amount of background activity. We investigated two different scatter window widths to be used with triple energy window (TEW) scatter correction. We also created multiple realizations of each configuration to improve our assessment, leading to a total of 540 simulations. Each configuration was imaged using a simulated Siemens SPECT camera. The projections were reconstructed using the standard 3D OSEM algorithm, and errors associated with 177Lu activity quantification and contrast-to-noise ratios (CNRs) were determined. In all configurations, the quantification error was within ± 6% of the no-90Y case, and we found that quantitative accuracy may slightly improve when 90Y is present because of reduction of errors associated with TEW scatter correction. The CNRs were not significantly impacted by the presence of 90Y, but they were increased when a wider scatter window width was used for TEW scatter correction. The width of the scatter windows made a small but statistically significant difference of 1-2% on the recovered 177Lu activity. Based on these results, we can conclude that activity quantification of 177Lu and lesion detectability is not degraded by the presence of 90Y.
“…Our study is unique as there have been no other simulation studies, to the best of our knowledge, performing SPECT imaging of 177 Lu and 90 Y combined. Dual-isotope SPECT imaging based on Monte Carlo simulations have been performed for radioisotope pairs such as 99m Tc/ 123 I [35] 123 I/ 125 I [36], and combinations of 99m Tc, 111 In, 123 I, 177 Lu, and 201 Tl [37], but not 177 Lu and 90 Y. Dosimetry simulations of 177 Lu and 90 Y therapy have been performed [38,39] which highlights the importance of a study such as ours; dosimetry is impractical outside of a simulation if imaging cannot be performed quantitatively. Imaging has been performed in dual-isotope PRRT with 177 Lu and 90 Y [40], but dosimetry was not performed.…”
This work aims to investigate the accuracy of quantitative SPECT imaging of 177Lu in the presence of 90Y, which occurs in dual-isotope radiopharmaceutical therapy (RPT) involving both isotopes. We used the GATE Monte Carlo simulation toolkit to conduct a phantom study, simulating spheres filled with 177Lu and 90Y placed in a cylindrical water phantom that was also filled with activity of both radionuclides. We simulated multiple phantom configurations and activity combinations by varying the location of the spheres, the concentrations of 177Lu and 90Y in the spheres, and the amount of background activity. We investigated two different scatter window widths to be used with triple energy window (TEW) scatter correction. We also created multiple realizations of each configuration to improve our assessment, leading to a total of 540 simulations. Each configuration was imaged using a simulated Siemens SPECT camera. The projections were reconstructed using the standard 3D OSEM algorithm, and errors associated with 177Lu activity quantification and contrast-to-noise ratios (CNRs) were determined. In all configurations, the quantification error was within ± 6% of the no-90Y case, and we found that quantitative accuracy may slightly improve when 90Y is present because of reduction of errors associated with TEW scatter correction. The CNRs were not significantly impacted by the presence of 90Y, but they were increased when a wider scatter window width was used for TEW scatter correction. The width of the scatter windows made a small but statistically significant difference of 1-2% on the recovered 177Lu activity. Based on these results, we can conclude that activity quantification of 177Lu and lesion detectability is not degraded by the presence of 90Y.
“…The primary issue would be to develop a method by which the gammas emitted from 125 I could be separated from any CT X-rays. One approach would be to use a Monte Carlo model that would enable a statistical method of removing the X-rays from the 125 I SPECT projection data, such as the GATE model created for this platform by Lee et al [ 17 , 18 ].…”
Multi-modality imaging provides coregistered PET-CT and SPECT-CT images; however such multi-modality workflows usually consist of sequential scans from the individual imaging components for each modality. This typical workflow may result in long scan times limiting throughput of the imaging system. Conversely, acquiring multi-modality data simultaneously may improve correlation and registration of images, improve temporal alignment of the acquired data, increase imaging throughput, and benefit the scanned subject by minimizing time under anesthetic. In this work, we demonstrate the feasibility and procedure for modifying a commercially available preclinical SPECT-CT platform to enable simultaneous SPECT-CT acquisition. We also evaluate the performance of simultaneous SPECT-CT tomographic imaging with this modified system. Performance was accessed using a 57Co source and image quality was evaluated with 99mTc phantoms in a series of simultaneous SPECT-CT scans.
“…We have recently developed methods for performing dualenergy studies using 125 I-and 123 I-labeled peptides that circumvent the confounding issues associated with low-energy X-ray emission from the latter. 15 With respect to the relatively greater hepatic and splenic uptake of SAP in the AA mice, we consider that these 2 highly vascularized, heavily amyloid-laden organs in the mouse sequestered the SAP, perhaps in a first-pass manor, and given that SAP irreversibly binds amyloid in the mouse, this prevented uptake in less accessible anatomic sites such as the intestines, pancreas, and likely the heart. This was not the case for p5þ14.…”
Section: Validationmentioning
confidence: 99%
“…We have recently developed methods for performing dual-energy studies using 125 I- and 123 I-labeled peptides that circumvent the confounding issues associated with low-energy X-ray emission from the latter. 15 …”
Amyloidosis is associated with a number of rare diseases and is characterized by the deposition, in abdominothoracic organs and peripheral nerves, of extracellular protein fibrils, which leads to dysfunction and severe morbidity. Effective clinical evaluation and management of patients with systemic amyloidosis are hampered by the lack of a noninvasive, quantitative method for detecting whole-body amyloid load. We have used a battery of assays including dual-energy SPECT imaging and comparative effectiveness studies in support of translation of a synthetic polybasic peptide, p5+14, as a novel radiotracer for visualization of amyloidosis by molecular imaging. These data provide support for a phase 1 positron emission tomography/computed tomography imaging trial of this reagent, labeled with iodine-124, in patients with all forms of systemic amyloidosis.
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