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Symbia intevo bold

Manufactured by Siemens
Sourced in Germany, United States

The Symbia Intevo Bold is a versatile medical imaging system designed for nuclear medicine applications. It combines single-photon emission computed tomography (SPECT) and computed tomography (CT) technologies to provide high-quality images for diagnostic and clinical purposes. The system's core function is to capture and integrate SPECT and CT data to support healthcare professionals in their clinical decision-making.

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10 protocols using symbia intevo bold

1

Quantitative SPECT/CT for Lu-PSMA Imaging

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Lu-PSMA images were acquired with SPECT/CT hybrid system Symbia Intevo Bold™ (Siemens Healthcare GmbH, Erlangen, Germany). Whole body scintigraphy was performed 0.5 h after injection and quantitative SPECT/CT (medium energy low penetration collimators, 60 views, time per view 15 s, continuous mode) from top of the head to mid-thigh was acquired 4, 24, and 48 h after injection. Quantitative SPECT reconstruction using xSPECT Quant™ (Broad Quantification) software with standardized CT attenuation, scatter and resolution recovery corrections was performed. Quantitative data about absolute tracer concentration in the body expressed in standardized uptake values (SUV), activity concentration (kBq/mL) or fraction of uptake (%) were acquired. The Dosimetry Research Tool software together with technical support was provided by Siemens Medical Solutions, USA, Inc., Hoffman Estates, IL, USA.
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2

Tc-99m-Labeled Tetragalactoside Imaging

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The [99mTc]Tc-TG, in a dose of 729 ± 102 MBq, was injected as an intravenous bolus. A Siemens Symbia Intevo Bold scanner was used for imaging. A high-resolution low-energy collimator was used to images acquisition. Anterior and posterior whole-body planar imaging (at a scan speed of 12  cm/min, 1024 × 256 pixel matrix) was carried out in patients 1–10 at 2, 4, 6 and 24 h after injection. All 12 patients received SPECT/CT scans (SPECT: 60 projections, 20 s each, 256 × 256 pixel matrix; CT: 130 kV, effective 36 mAs) at 2 h and only SPECT scans (60 projections, 20 s each, 256 × 256 pixel matrix) 4 and 6 h after injection. For SPECT reconstruction, the xSPECT (Siemens) protocol based on the ordered subset conjugate gradient (OSCG) method (24 iterations, 2 subsets) was used. The 3D Gaussian FWHM 10 mm filter (Soft Tissue) was used. For processing of obtained images, the proprietary software package syngo.via (Siemens) was used.
Vital signs were monitored before, during and after imaging. Parameters of blood biochemistry were analyzed before injections of [99mTc]Tc-TG and 24, 48 h and 7 days after injections.
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3

CT Electron Density Phantom Analysis

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CT images were acquired with a SPECT/CT hybrid system (Symbia Intevo Bold, Siemens Healthineers) with adjustable CT voltage (80, 110, and 130 kVp). The protocol DE Abdomen (80 and 130 kVp) was used for imaging all phantoms used in this study. All CT reconstructions were performed with the I41s kernel (iterative reconstruction).
The Segment Editor module of 3D Slicer (version 4.8.1) [18] (link), [19] was used to analyze the CT images of the CT electron density phantom Model 062M (computerized imaging reference systems, CIRS) and the European Spine Phantom [20] (link). All mathematical calculations were performed in R (version 3.5.1) [21] .
The chemical formula and density of the materials used for quantification are described in the supplemental material Table 1. The elemental mass fractions of each compound or mixture were obtained using the XCOM online tool offered by the National Institute of Standards and Technology (NIST) [22] . In case of the CIRS phantom, the manufacturer provided the elemental composition, elemental mass fractions, and mass densities of the phantom materials.
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4

Radiotracer-Guided Lung Nodule Marking

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Chiva needles of 22-G and 9 or 16 cm in length (BD, Madrid, Spain) were used for marking. The tip of the needle was placed inside the nodule under CT fluoroscopy guidance, and the radiotracer was injected ([99mTc]Tc-MAA, 37–111 MBq, 0.2 mL; depending on whether the injection was performed on the same-day surgery or the previous one) mixed with 1 mL of iodinated contrast. Next, a new CT was performed to check the iodinated contrast’s location and evaluate potential complications. Subsequently, a single-photon emission CT/CT (SPECT/CT) (InfiniaTM HawkeyeTM 4; GE Healthcare Milwaukee, WI, USA or Symbia Intevo Bold; Siemens Healthineers, Erlangen, Germany) with volumetric reconstruction was performed to verify the location of the radiotracer.
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5

PSMA-PET/CT and SPECT/CT Dosimetry

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[68Ga]Ga-PSMA-PET/CT imaging was performed on a Biograph mCT system (Siemens Healthineers, Erlangen, Germany) 1 week prior to each administration of [177Lu]Lu-PSMA to evaluate PSMA-positive tumor lesions, following local clinical acquisition protocols [30 (link)]. Standardized uptake values (SUV) were determined for salivary gland (SUVmean, spherical volumes of interest (VOIs) of 20 mm in diameter) and lesions (SUVmax). For dosimetry, all patients received SPECT/CT imaging at 1, 24, 48, 72, and 168 h after each therapy on either a Symbia T16 or Symbia Intevo Bold system (Siemens Healthineers, Erlangen, Germany). Both systems were cross-calibrated for 177Lu with the in-house dose calibrator, which undergoes regular quality control according to national guidelines [31 ]. Three-bed position SPECT/CT scans were acquired including the pelvis, abdomen, and head/neck region. The acquisition and reconstruction protocol was followed as described by Peters et al. [32 (link)] and was in accordance with MIRD pamphlet no. 26 [33 (link)]. These protocols take into account scatter, attenuation, and dead-time corrections.
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6

99mTc-MIBI Parathyroid Imaging Protocol

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Imaging acquisition was performed on a double-head gamma-camera equipped with low-energy high-resolution (LEHR) collimators (Siemens Symbia Intevo Bold). After injection of 555 MBq (15 mCi) of 99mTc- MIBI, early and delayed parathyroid scans were obtained 15 min (min) and 2 h (h) after the injection, respectively. Anterior neck images were obtained in a 256 × 256 matrix, gathering 500 k counts per position, with a 20% energy window centered on the 140 keV photopeak after 15 min and 2 h. SPECT/CT imaging was performed immediately after both the early and delayed planar images. During the SPECT study, 30 stops were acquired, with 20 s acquisition time per frame and a matrix of 256 × 256 pixels. CT images were acquired with the tube voltage set at 100 kV, tube current determined by automatic dose modulation with a set reference current of 60 mAs.
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7

Dual-Tracer Imaging Protocol for ADAPT6 and (HE)3-G3 in Cancer Patients

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Each patient was injected with [99mTc]Tc-ADAPT6, followed by injection with [99mTc]Tc-(HE)3-G3 after 3–4 days. In patient 1, the interval between injection was 15 days.
The injected protein masses and timing of imaging were selected based on the results of previous Phase I studies [9 (link),10 (link)]. The injected protein masses were 500 and 3000 µg for [99mTc]Tc-ADAPT6 and [99mTc]Tc-(HE)3-G3, respectively. [99mTc]Tc-ADAPT6 (523 ± 211 MBq) and [99mTc]Tc-(HE)3-G3 (443 ± 185 MBq) were injected intravenously. Imaging was performed using a Siemens Symbia Intevo Bold scanner equipped with a high-resolution low-energy collimator. SPECT/CT scans (SPECT: 60 projections, 20 s each, stored in 256 × 256 pixel matrix/CT: 130 kV, effective 36 mAs) were performed 2 h after injection for [99mTc]Tc-ADAPT6 and 4 h after injection for [99mTc]Tc-(HE)3-G3 in all patients. SPECT images were reconstructed using a reconstruction xSPECT (Siemens) protocol based on the ordered subset conjugate gradient (OSCG) method (24 iterations, 2 subsets). The 3D Gaussian FWHM 10 mm filter (Soft Tissue) was used. The images were processed using the proprietary software package Syngo.via (Siemens).
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8

Pediatric SPECT-CT System Comparison

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Data were gathered on two different SPECT-CT systems. The first scanner used in this study was a Symbia T16 (Siemens Healthineers, Hoffman Estates, IL, USA), using a 16-slice Emotion CT subsystem. This scanner operated on software version VA60D (using syngo CT software version 2007E), which utilised a 20 kg child CARE Dose 4D modulation reference. The second scanner was a Symbia Intevo Bold (Siemens Healthineers, Hoffman Estates, IL, USA), using a 16-slice Scope Power CT system. This scanner operated on software version VB20B (using syngo CT software version VC30), which utilised a 75 kg adult dose modulation reference. The Emotion and Scope Power are almost identical in their standard configuration, with choice of protocol settings and behaviour being very similar [9 ,10 ], with the exception that the minimum tube current was 20 mA on the Symbia T16 and 25 mA on the Symbia Intevo Bold. This, together with a tube rotation time of 0.6 s and pitch of 1.5 translates to minimum deliverable effective mAs of 8 on the Symbia T16 and 10 on the Symbia Intevo Bold.
The measurements in this study were made using the Paediatric Whole Body phantom PBU 70 (Kyoto Kagaku Co., Ltd, Kyoto, Japan), which represents a 20 kg child.
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9

PSMA-RLT Dosimetry Protocol for Prostate and SGC Cancers

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In a third-line academic institute (Radboudumc, the Netherlands), two prospective clinical studies were conducted on PSMA-RLT in cancer patients with PSMA-positive disease and an adequate glomerular filtration rate (GFR) (≥50 mL/min). Both studies used an identical dosimetry protocol. One study applied a first cycle of 3 GBq and a second cycle (after 6 weeks) of ~6 GBq [177Lu]Lu-PSMA-617 in ten low-volume metastatic hormone-sensitive prostate cancer (mHSPC) patients, thus in total a cumulative activity of ~9 GBq [7 (link)]. The other used ~7.4 GBq [177Lu]Lu-PSMA-I&T in 10 advanced SGC patients (NCT04291300). The dosimetry protocol of both trials consisted of five time points (1 h, 24 h, 48 h, 72 h, and 168 h) 3D SPECT/CT imaging post [177Lu]Lu-PSMA injection. All scans were acquired on a Symbia T16 or Symbia Intevo Bold system (Siemens Healthineers, Erlangen, Germany) using a medium-energy low-penetration collimator, a 20% photon energy window at 208 keV with dual-energy window for Compton scattering, 64 projections per detector and 14 s per projection, matrix size 128 × 128 and zoom 1. Data were reconstructed using ordered subsets maximization expectation reconstruction (Flash 3D with collimator detector response) using four iterations, eight subsets and a smoothing Gaussian filter of 8.4 mm.
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10

Imaging and Radioligand Therapy for Prostate Cancer

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Patients received [68Ga]Ga-PSMA-11-PET/CT approximately 1 week prior to radioligand therapy. Imaging was performed 60 ± 10 min post-injection on a Biograph mCT system (Siemens Healthineers, Erlangen, Germany) scanning cranium to trochanter major. Patients received a therapeutic activity of 3 GBq (3057 ± 38 MBq) [177Lu]Lu-PSMA-617. This relatively low activity was chosen because it was part of a prospective pilot study in a patient population that did not receive this type of treatment before. The preparation of [177Lu]Lu-PSMA was described previously [25 ] and can be found in Online Resource 2. SPECT/CT imaging was performed at 1, 24, 48, 72, and 168 h after administration on either a Symbia T16 or Symbia Intevo Bold system (Siemens Healthineers, Erlangen, Germany). SPECT/CT scans were acquired at three body regions: pelvis, abdomen, and head-neck regions. Acquisition and reconstruction parameters can be found in Online Resource 3.
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