Accurate dose predictions are crucial to maximizing the benefits of carbon-ion therapy. Carbon beams incident on the human body cause nuclear interactions with tissues, resulting in changes in the constituent nuclides and leading to dose errors that are conventionally corrected using conventional single-energy computed tomography (SECT). Dual-energy computed tomography (DECT) has frequently been used for stopping power estimation in particle therapy and is well suited for correcting nuclear reactions because of its detailed body-tissue elemental information. This study proposes a correction method for the absolute dose in carbon-ion therapy that considers changes in nuclide composition resulting from nuclear reactions with body tissues, as a novel application of DECT. Approach: The change in dose associated with nuclear reactions is determined by correcting each integrated depth dose component of the carbon beam using a nuclear interaction correction factor. This factor is determined based on the stopping power, mass density, and nuclear interaction cross-section in body tissue. The stopping power and mass density were calculated using established methods, whereas the nuclear interaction cross-section was newly defined through a conversion equation derived from the effective atomic number. Main results: Nuclear interaction correction factors and corrected doses were determined for 85 body tissues with known compositions, comparing them with existing SECT-based methods. The root-mean-square errors of the SECT- and DECT-based nuclear interaction correction factors relative to theoretical values were 0.66% and 0.39%, respectively. Significance: This indicates a notable enhancement in the estimation accuracy with DECT. The dose calculations in uniform body tissues derived from SECT showed slight over-correction in adipose and bone tissues, whereas those based on DECT were almost consistent with theoretical values. Our proposed method demonstrates the potential of DECT for enhancing dose calculation accuracy in carbon-ion therapy, complementing its established role in stopping power estimation. .
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http://dx.doi.org/10.1088/1361-6560/adaad4 | DOI Listing |
J Exp Clin Cancer Res
January 2025
Department of Pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Avenue, Wuhan, 430022, Hubei Province, People's Republic of China.
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Pediatr Nephrol
January 2025
Department of Nephrology, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Center), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China.
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Nat Commun
January 2025
Laboratory of Pathogens and Host Immunity, UMR 5294 CNRS, UA15 INSERM, Université de Montpellier, Montpellier, 34095, France.
Programmed-cell death is an antimicrobial defense mechanism that promotes clearance of intracellular pathogens. Toxoplasma counteracts host immune defenses by secreting effector proteins into host cells; however, how the parasite evades lytic cell death and the effectors involved remain poorly characterized. We identified ROP55, a rhoptry protein that promotes parasite survival by preventing lytic cell death in absence of IFN-γ stimulation.
View Article and Find Full Text PDFInt Dent J
January 2025
Hunan Key Laboratory of Oral Health Research, Hunan Clinical Research Center of Oral Major Diseases and Oral Health, Xiangya Stomatological Hospital, Xiangya School of Stomatology, Central South University, Changsha, Hunan, China. Electronic address:
Introduction And Aims: Oral squamous cell carcinoma (OSCC) is one of the most prevalent malignancy of the head and neck. Early diagnosis of OSCC is difficult and the prognosis has not improved significantly. This study aims to explore the role of tubulin polymerisation promoting protein 3 (TPPP3) in the occurrence and development of OSCC and discover new diagnostic and prognostic markers for OSCC.
View Article and Find Full Text PDFJ Nucl Med Technol
January 2025
Department of Radiology and Nuclear Medicine, University Hospital of Southern Denmark, Esbjerg, Denmark.
Gated equilibrium radionuclide angiography (ERNA), or multigated acquisition scanning, is a well-established technique to monitor left ventricular ejection fraction (LVEF) in patients treated with potentially cardiotoxic chemotherapy. To determine the results of a true change in LVEF, low inter- and intrareader variability is important. The aim of this study was to investigate inter- and intrareader variability in LVEF measurements using 2 different commercially available software packages with cardiac MR (CMR) as a reference standard.
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