Background: The study aimed to compare normal oesophageal wall thickness based on 3-dimensional computed tomography (3DCT), 4-dimensional computed tomography (4DCT) and cone beam computed tomography (CBCT).
Methods: Contrast-enhanced 3DCT, 4DCT, and CBCT scans were acquired from 50 patients with lung cancer or metastatic lung cancer. The outer oesophageal wall was manually contoured on each 3DCT, the maximum intensity projection of 4DCT (4DCTMIP) the end expiration phase of 4DCT (4DCT50) (the end expiration phase of 4DCT) and the CBCT data sets.
Background: Concurrent chemoradiotherapy is considered curative intent treatment for patients with non-operative esophageal cancer. Radiation-induced heart damage receives much attention. We performed repeated four-dimensional computed tomography (4DCT) to detect changes in cardiac volume during radiotherapy for esophageal cancer patients, and explored potential factors responsible for those changes.
View Article and Find Full Text PDFBackground: To explore motion information included in 3DCT, 4DCT and CBCT by comparing volumetric and positional differences of GTV.
Results: Independent of tumor location, significant differences were observed among volumes [IGTV > (IGTV or IGTV) > (GTV or GTV)]. The underestimations or overestimations between IGTV and IGTV were larger than those between IGTV and IGTV ( < 0.
Purpose: To compare planning target volume (PTV) defined by PET combined with 4DCT to 3DCT and 4DCT.
Methods: Eighteen (18/30) esophageal cancer patients who underwent 3DCT, 4DCT and (18)F-FDG PET-CT thoracic simulation with SUVmax≥2.0 of the primary volume were enrolled.
Background: To determine the optimal threshold of 18 F-fluorodexyglucose (18 F-FDG) positron emission tomography CT (PET/CT) images that generates the best volumetric match to internal gross target volume (IGTV) based on four-dimensional CT (4DCT) images.
Methods: Twenty patients with non-small cell lung cancer (NSCLC) underwent enhanced three-dimensional CT (3DCT) scan followed by enhanced 4DCT scan of the thorax under normal free breathing with the administration of intravenous contrast agents. A total of 100 ml of ioversol was injected intravenously, 2 ml/s for 3DCT and 1 ml/s for 4DCT.
We described in the paper a new high-throughput screening method for Cys282Tyr mutation in hereditary haemochromatosis with double-stranded probe using synchronous fluorometry. The probe for wild type was labeled with Fam, the probe for mutant type was labeled with Joe. After PCR, reaction tubes were transferred to a spectrofluorometer, where synchronous spectra were scanned in a constant-wavelength mode.
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