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Biograph mct 64 pet ct

Manufactured by Siemens
Sourced in Germany

The Biograph mCT-64 is a positron emission tomography/computed tomography (PET/CT) system manufactured by Siemens. It combines high-resolution PET imaging with fast, state-of-the-art CT imaging to provide comprehensive diagnostic information. The system features a 64-slice CT scanner and advanced PET technology to deliver high-quality imaging for a range of clinical applications.

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10 protocols using biograph mct 64 pet ct

1

PET/CT Imaging Protocol for Neuroblastoma

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Patient gender, age, neuron-specific enolase (NSE), serum ferritin (SF), lactate dehydrogenase (LDH), vanillylmandelic acid (VMA), homovanillic acid (HVA), maximum tumor diameter (MTD) in Ultrasound, and MTD in CT and/or MRI.
All patients underwent whole body scan on the PET/CT scanner (Biograph mCT-64 PET/CT; Siemens, Knoxville, Tenn) in accordance with EANM guidelines (19 (link), 20 (link)) and a biopsy/surgery for pathological diagnosis of NB was performed within 3 months. The PET scan was carried out with 3 min per bed position immediately after the whole body CT scan. PET images were reconstructed using the ordered subsets-expectation maximization algorithm with time-of-flight. The regions-of-interest (ROIs) of primary tumor were manually drawn by an experienced nuclear medicine physician using the longitudinal PET/CT module in 3D Slicer (version 4.10.1). ROIs were delineated along the edge of NB on CT images, which included the entire tumor, metastatic lesions and unclear demarcations between the primary tumor and its surrounding metastasis. In order to map to the PET image, the ROIs were resampled based on B-spline interpolation to ensure that it had the same pixel spacing as the PET image.
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2

PET/CT Imaging Protocol for 18F-FDG

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18F-FDG is produced by Japan’s Sumitomo Cyclotron HM-10HC, and ensuring each batch of drugs meets the requirements through strict quality control. The imaging equipment is Siemens Biograph mCT-64 PET/CT. Before the examination, the patient fasted for more than 6 h, was monitored the fasting blood glucose level, injected 18F-FDG intravenously in a quiet state, with the dose range of 3.7–5.55 MBq (0.10–0.15 mCi)/kg, and was instructed to drink more water and urinate. After the imaging agent is injected, the patient rests quietly for 40–60 min. Before the examination, the bladder was emptied, and then 300–500 mL water was drunk to fill the stomach. First, the patients underwent  CT full-body scan (voltage 120 kV, current through 3D automatic real-time control by milliampere technology, CT scan with a thickness of 5 mm), and then whole-body PET collection, with the scan range from the top of the head to the upper femur. The PET scan is generally 6–7 beds, each bed is collected for 1.5 min, and the entire scanning process is about 15 min. Attenuation correction is performed on the collected data. The PET/CT whole-body imaging adopts the ordered subset maximum expected value method (OS-EM) for image reconstruction and transmits it to the Syngo MI workstation for image fusion.
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3

PET/CT Protocol for Oncology Planning

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Pre-treatment 18F-FDG PET/CT (Biograph mCT-64 PET/CT; Siemens) scans were acquired in radiation treatment planning position. Patients were instructed to fast except for the consumption of water for at least 6 h before scanning. Images were acquired 60 min after the intravenous injection of 3 MBq/kg 18F-FDG. 18F-FDG PET images were obtained within 2–3 min per bed position in three-dimensional setting. Images were reconstructed using a time-of-flight iterative reconstruction method (three iterations; 21 subsets) with point-spread-function correction [29 (link)]. Images were corrected for random coincidences, scatter, and attenuation (CT-based), and were smoothed with a Gaussian filter of 6.5 mm in full-width at half-maximum.
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4

Pediatric 18F-FDG PET/CT Imaging Protocol

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All patients in the cohort underwent whole body 18F-FDG PET/CT (Biograph mCT-64 PET/CT, Siemens Medical Solution) scans according to European Association of Nuclear Medicine guidelines for children tumor imaging at baseline (before starting chemotherapy) (17 (link)). Patients were instructed to fast for at least 6 hours, to make the blood glucose level under 11.1 mmol/L before the 18F-FDG injection. A mean dose of about 3.7 MBq/kg (0.10 mCi/kg) was administrated, considering the patients were children. If needed, infants were sedated using chloral hydrate 40 minutes after the 18F-FDG injection. About an hour after the injection, a low-dose CT scan (tube voltage 120 keV, thickness 3 mm) was performed for viewing anatomic structures and attenuation correction. A PET scan was performed immediately after CT acquisition in a three-dimensional (3D) mode (2 min/bed position). PET images were reconstructed with the time-of-flight ordered subsets-expectation maximization algorithm.
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5

Neoadjuvant Chemoradiotherapy for Esophageal Cancer

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Patients were staged with a thoraco-abdominal CT (Biograph mCT 4–64 PET/CT; Siemens, Erlangen, Germany), 18F-FDG PET/CT (Biograph mCT-64 PET/CT; Siemens, Knoxville, TN, USA), and endoscopic ultrasound. Patients were discussed in the multidisciplinary upper gastrointestinal tumor board and treated according to the CROSS regimen (5 cycles of carboplatin (2 mg∙min∙mL−1) and paclitaxel (50 mg/m2) with 41.4 Gy in 23 fractions) [1 (link)]. Restaging was performed 6–8 weeks after nCRT with CT (before 2014) or 18F-FDG PET/CT (after 2014). Surgical treatment consisted of a minimally invasive or open transthoracic esophagectomy.
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6

Pediatric Whole-Body 18F-FDG PET/CT Imaging Protocol

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All patients in the cohort underwent whole body 18F-FDG PET/CT (Biograph mCT-64 PET/CT; Siemens, Knoxville) scans according to European Association of Nuclear Medicine guidelines for tumor imaging [17 (link), 18 (link)]. Patients were instructed to ban from intense exercises for at least 24 h before PET/CT scan and fast at least 6 h before 18F-FDG injection. A mean dose of 3 mCi (mean 0.14 mCi/kg) was administrated considering the patients are children. A low-dose CT scan (CT scanning parameters: tube voltage 120 keV, thickness 2 mm, matrix size 512 × 512) for viewing anatomic structures and attenuation correction was performed an hour after the injection. PET scan with three-dimension image mode and 2 min per bed setting followed immediately after CT acquisition. PET images were reconstructed with the time-of-flight ordered subsets-expectation maximization algorithm. All corrections for quantitative interpretation, including detector sensitivity normalization, dead time, random, scatter, attenuation and decay correction were applied during reconstruction. A Gaussian smoothing filter with a full width at half-maximum of 5 mm was applied to the PET images. The PET images’ parameters were as follows: pixel size 4.07 mm × 4.07 mm, 3 mm slice thickness, and matrix size 200 × 200.
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7

Whole-Body 18F-FDG PET/CT Imaging Protocol

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All patients underwent whole body (from vertex to toes) scan on the PET/CT scanner (Biograph mCT-64 PET/CT; Siemens, Erlangen, Germany) in accordance with European Association of Nuclear Medicine guidelines (17 (link)). Before the injection, they were told to stop any vigorous exercise for at least 24 hours and fast for at least 6 hours. A quantity of 0.14 mCi/kg of 18F-FDG (provided by Beijing Atomic High-tech Co., Ltd., Beijing, China) was injected intravenously 40–60 minutes before the PET/CT scan. First, a low-dose CT scan could use an automated modulated tube current and 120 kV tube voltage was carried out for anatomical reference and attenuation correction. The CT image parameters were as follows: pixel size 0.586×0.586 mm, 2 mm slice thickness, and matrix size 512×512. The whole-body CT scan was followed immediately by a 2-minute PET scan for each bed position. PET images were reconstructed using time-of-flight (ToF) and the ordered subsets-expectation maximization (OSEM) technique. Attenuation corrections were applied during the reconstruction and a 5 mm Gaussian filter was applied to the PET images. The PET image parameters were as follows: pixel size 4.07×4.07 mm, 3 mm slice thickness, and matrix size 200×200.
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8

Standardized PET/CT Imaging Protocol

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18F-FDG is produced by Japan’s Sumitomo Cyclotron HM-10HC, which ensures each drug batch meets the requirements through strict quality control. The imaging equipment is a Siemens Biograph mCT-64 PET/CT. Before the examination, the patient fasted for more than 6 h, monitored the fasting blood glucose level, and was injected with 18F-FDG intravenously in a quiet state. The injection dose was 0.10–0.15mCi/kg and the patient was instructed to drink more water and urinate. After the imaging agent was injected, the patient rested quietly for 40–60 min. Before the examination, he emptied the bladder and drank 300–500 ml of water to fill the stomach. It is recommended to choose the correct scanning protocol for image acquisition to perform a full-body CT scan (voltage 120 kV, current through 3D automatic real-time control by milliampere technology and CT scan with a thickness of 5 mm), and then collect whole-body PET, with the scan range from the top of the head to the upper femur. The PET scan has 6–7 beds, each bed is collected for 1.5 min, and the entire scanning process takes about 15 min. Attenuation correction is performed on the collected data. The PET/CT whole-body imaging adopts the ordered subset maximum expected value method (OS-EM) for image reconstruction and transmits it to the Syngo MI workstation for image fusion.
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9

PET/CT Imaging Protocol for Tumor Assessment

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All of the patients underwent PET/CT (Biograph mCT-64 PET/CT; Siemens, Knoxville, TN, USA) examinations following European Association of Nuclear Medicine guidelines for tumor imaging [18 (link),19 (link)]. They were instructed to fast for at least 6 h and decrease intense exercises for at least 24 h, and 0.10–0.15MBq/kg of 18F-FDG was intravenously injected 40–60 min before the PET/CT scan. A low-dose CT scan (CT scanning characteristics: tube voltage 120 keV, resolution 0.586 × 0.586 mm, thickness 2 mm, matrix size 512 × 512) for viewing anatomic reference and attenuation correction was performed firstly, followed by PET scan. PET scan was performed with 3-dimension image mode and 2 min per bed position immediately after CT. The ordered subsets-expectation maximization algorithm in a time-of-flight based iterative reconstruction method was used for PET images reconstruction. All corrections, including detector efficiency, normalization, dead time, random counts, scatter, attenuation, were applied during reconstruction. A Gaussian smooth filter of 5 mm in full width at half-maximum was applied to the PET image.
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10

PET/CT Imaging Protocol for Disease Evaluation

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All patients underwent PET/CT whole-body scans (Biograph mCT-64 PET/CT; Siemens) according to the European Association of Nuclear Medicine (EANM) guidelines (15 (link),16 (link)). Prior to the scan, they were asked to fast for at least 6 h and to reduce high-intensity exercise for at least 24 h. 18F-FDG 0.10–0.15 MBq/kg (provided by Beijing Atomic Technology Co., Ltd.) was injected intravenously 40–60 min before the PET/CT scan. A low-dose CT scan with anatomical reference and attenuation correction was first performed with a tube voltage of 120 kV and automatic tube current modulation. The CT imaging parameters were as follows: resolution 0.586 mm × 0.586 mm, slice thickness 2 mm, and matrix size 512×512. The whole-body CT scan was immediately followed by a PET scan for 2 min in each bed. The ordered subset expectation maximization (OSEM) algorithm with time of flight (TOF) was used to reconstruct the PET images. The PET imaging parameters were as follows: resolution 4.07 mm × 4.07 mm, slice thickness 3 mm, and matrix size 200×200.
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