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Syngo trued

Manufactured by Siemens
Sourced in Germany

Syngo TrueD is a software solution developed by Siemens for medical imaging and analysis. It provides advanced three-dimensional visualization and quantification capabilities for various imaging modalities, including CT, MRI, and PET.

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11 protocols using syngo trued

1

PET/CT-based Tumor Volume Quantification

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Volumes were measured on PET/CT acquisitions using a dedicated FDA approved software program (TrueD-Syngo, Siemens AG, Germany). A spherical box was positioned around the phantom insert mimicking the tumoral lesion to define a volume of interest (VOI). The MTV was then automatically calculated by a standardized routine program applying a fixed threshold (FT) algorithm. The tumour volume was delineated by all the voxels within the initial VOI with SUV values above or equal to the fixed threshold [35] . We tested the methods by applying three thresholds recently proposed in the literature for lymphomas: 25%, 41% of the SUVmax and an absolute SUV value of 2.5 (FT25%, FT41%, FT2.5) [29, (link)30, (link)33, (link)36] (link). In addition, the MTV calculation was also obtained by means of a region growing (RG) algorithm (3D Freeform Isocontour tool, TrueD Syngo, Siemens AG, Germany), with automatically segmented volume including all the voxels with common characteristics [37] . In PET images, after the selection of the tumor central voxels, all the neighboring voxels were automatically included in the segmented volume according to the voxel intensity. The algorithm was applied in contrast mode not requiring a predefined threshold [38] (link).
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2

PET/CT Imaging of Prostate Cancer

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Image analysis was performed using an appropriate workstation and software (Syngo TrueD, Siemens, Erlangen, Germany). Clinical PET/CT reading was performed by three experienced specialists from the department of nuclear medicine and from the department of radiology in consensus in a side-by-side analysis of the results obtained with both tracers. Lesions were visually interpreted as suspicious for local relapse, lymph node metastasis, bone metastasis, or visceral metastasis.
The standardized uptake value (SUV)max was measured in up to three hottest lesions (as identified in the [68Ga]Ga-PSMA-HBED-CC scan) and their counterpart in the [18F]DCFPyL scan. Background SUVmean values were measured in a volume of interest (VOI) with 2 cm diameter in the liver, spleen, kidney, mediastinum, and parotid in all patients. For the calculation of mean values and to compare the SUVmax values of the lesions and their ratios, SPSS 22 was used.
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3

PET/CT Imaging of Brain and Body with Ga-68/Bi-213-DOTA-SP

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A three-dimensional mode was used for PET/CT examinations performed on a Biograph 64 TruePoint PET/CT scanner (Siemens Medical Solutions, Knoxville, TN), 30 min after the co-injection of 68Ga/213Bi –DOTA-SP. Five minutes acquisition time was used for PET of brain and 2 min acquisition per bed position for body (from the neck to the upper thighs).
The PET image data were corrected for scatter and attenuation using the CT data and reconstructed in a 168 × 168 matrix. The reconstruction was performed using the TrueX algorithm (Siemens Medical Solutions) with PSF, three iterations, 21 subsets, and no post filtering.
The PET/CT images (half-body-attenuated and non-attenuated PET, CT, and fused images) were transferred to a multimodal work station (MMWS; Syngo TrueD; Siemens Medical Solutions) for analysis.
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4

Quantitative PET Analysis of Developmental Venous Anomalies

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The MR and PET images were co-registered using Syngo.via and Syngo TrueD systems (Siemens Healthcare, Malvern, PA) software, which was then used for the measurement of the average standardized uptake value (SUV) in a 1 cm3 spherical region of interest (ROI) around the visually determined lesions and in the anatomically equivalent contralateral brain region. The SUV represents the radioactivity concentration observed in an ROI relative to the hypothetical case of homogeneous distribution of the injected radioactivity across the entire body of the patient. In this study, SUVDVA is defined as the mean SUV from the region of the DVA divided by the mean SUV in the anatomically equivalent contralateral region. The size of each DVA was measured as the single longest dimension of the aberrant vasculature. The qualitative characterization of the degree of metabolic abnormality (mild, moderate, or severe hypometabolism; isometabolism; or mild, moderate, or severe hypermetabolism) was determined by a consensus of the authors.
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5

Quantitative PET Image Analysis for PCa

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An experienced nuclear medicine specialist, who also identified all PCa lesions in the pelvis, qualitatively evaluated the reconstructed PET images. For a quantitative assessment, we analyzed the SUVmean and SUVmax for each detected lesion located in the entire pelvis, as well as the SUVmean of its respective background (BG), using the PERCIST reference volumes of interest with commercial software (syngo TrueD, Siemens Healthcare, Erlangen, Germany).
In the absence of absolute ground truth data, the results were compared using linear regression against standard Dixon-VIBE, which was available on the system from the very beginning. Additionally, the Wilcoxon signed-rank tests were performed to test whether the SUVmean and SUVmax values in PET images reconstructed using each AC method were significantly different from the corresponding values in the PET images reconstructed with other evaluated methods. We investigated variance and correlation between the methods and calculated the coefficient of correlation r as well as the coefficient of determination R2 (“R squared”) for each evaluated method against standard Dixon-VIBE. The differences between the AC methods, i.e., the estimated bias and fluctuations in SUVmax, were additionally visualized and evaluated using the Bland-Altman plots (the agreement limits were defined by the 96% confidence level).
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6

Myocardial 18F-FDG PET/CT and PET/MR Comparison

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Three-dimensional image co-registration and fusion of PET and MR imaging data were performed using dedicated postprocessing software for hybrid imaging (Syngo TRUE-D; Siemens Healthcare). Co-registration was performed by automatic algorithm registration using MR images as the source image for co-registration. Images were assessed blindly by a single reader (JML). Average myocardial SUVs were obtained by tracing the entire cross section of the left ventricular myocardium in the transaxial orientation of the heart at the mid-ventricular level (Figure 1). Average values with standard deviations are reported. Significance testing between the average myocardial 18F-FDG PET SUVs acquired on PET/CT and PET/MR imaging was performed by using paired 2-tailed t tests. A P value < 0.05 was considered significant. Agreement between SUVs acquired on PET/CT and PET/MR imaging was estimated with the Spearman correlation coefficient in a scatter plot, and coefficient of variation was graphically analyzed by a Bland-Altman plot.
Of note, as per standard PET/CT and PET/MR imaging, the patients’ arms were raised during PET-CT data acquistion, whereas in PET/MR, the arms were to the side of the body. MLAA correction was performed to account for the difference in arm positions and tissue attenuation effect.
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7

FDG-PET Quantitative Measurements of Lung Lesions

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Quantitative measurements were performed on a dedicated workstation (Syngo TrueD, Siemens Medical Solutions).
Volume of interest (VOI) was performed using a 40% threshold of SUVmax. The SUVmax, SUVmean and MTV were obtained for each identified lung lesion. TLG defined as MTV multi-plied by the average SUV uptake (SUVmean) within the MTV. We used the liver as a source for the background and noise measurement [13 (link)]. In each patient, a 30 mm-diameter spherical VOI was placed within an area of uniform FDG distribution in the liver, the mean SUV and standard deviation within the VOI were obtained. The signal-to-nose ratio of the tumour, relative to the liver, SNR (T–L) was calculated as: SNR(T-L)=Tumour-LiverSDL where the Tumour refers to SUVmax in the lung lesion, Liver and SDL is the mean SUV and standard deviation measured in the liver VOI respectively.
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8

Whole-Body 68Ga-PSMA-11 PET/CT Imaging Protocol

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Whole‐body scans were performed by using a combined PET/CT system (Siemens Biograph mCT.X, Siemens AG, Munich, Germany). Patients did not need to fast before the examination but had to drink 500 ml of water within 2 h to ensure sufficient hydration. To reduce urinary radioactivity, the bladder was emptied before imaging. Whole‐body images were collected 60 to 90 min after injection of 0.05 mCi/kg 68GA‐PSMA‐11. The scanning range was from the base of the skull to the middle of the femur, and local collection was performed if necessary. Low‐dose CT‐scanning was mainly used for attenuation correction and lesion localization in PET images. Automatic milliampere‐control technology was used for diagnostic CT scanning. PET was conducted in 3D mode for 3 min per bed position. If the lesion was not clear in the initial images, delayed imaging was performed 3 to 4 h later. A syngo TrueD (Siemens AG) workstation was used for the registration and fusion of the acquired images from the PET and CT scans. Corrections were applied for random effects, geometry, attenuation and scatter.
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9

Quantifying Myocardial 18F-FDG Uptake and Scar

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In order to determine the 18F-FDG extent, a region grow algorithm with a threshold of 50% of the maximal uptake was performed (Syngo MMWP [workstation], Syngo TrueD [software]; Siemens Healthcare). Within this volume of interest (VOI), the average tracer uptake was derived and normalized to the lean body mass and injected tracer dose yielding SUVmean.23 The volume with tracer uptake above the mentioned threshold was finally expressed as %LV (LV myocardial volume derived from MRI) and defined as 18F-FDG extent (i.e. the volume of the significant 18F-FDG signal normalized to the total myocardial volume of the LV). SUVmean in remote myocardium was determined in manually drawn regions in the myocardial wall opposing the infarct on 3 consecutive slices.
The LGE extent of the LV myocardium was determined by manual delineation on short axis images using the MunichHeart/MR software and expressed as percentage of the left ventricle.
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10

PET/CT Image Analysis Guideline

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PET/CT Images will be reviewed and analyzed using Siemens Syngo/TrueD and OSIRIX workstations by a board certified nuclear medicine physician and a board certified radiologist experienced in reading PET/CT using recent reporting guidelines (PROMISE criteria, miTNM standardized framework) [50 (link)].
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