Current phantoms used for the dose reconstruction of long-term childhood cancer survivors lack individualization. We design a method to predict highly individualized abdominal three-dimensional (3-D) phantoms automatically. We train machine learning (ML) models to map (2-D) patient features to 3-D organ-at-risk (OAR) metrics upon a database of 60 pediatric abdominal computed tomographies with liver and spleen segmentations. Next, we use the models in an automatic pipeline that outputs a personalized phantom given the patient's features, by assembling 3-D imaging from the database. A step to improve phantom realism (i.e., avoid OAR overlap) is included. We compare five ML algorithms, in terms of predicting OAR left-right (LR), anterior-posterior (AP), inferior-superior (IS) positions, and surface Dice-Sørensen coefficient (sDSC). Furthermore, two existing human-designed phantom construction criteria and two additional control methods are investigated for comparison. Different ML algorithms result in similar test mean absolute errors: for liver LR, IS, and spleen AP, IS; for liver AP and spleen LR; for abdomen sDSC; and to 65% for liver and spleen sDSC. One ML algorithm (GP-GOMEA) significantly performs the best for 6/9 metrics. The control methods and the human-designed criteria in particular perform generally worse, sometimes substantially ( error for spleen IS, sDSC for liver). The automatic step to improve realism generally results in limited metric accuracy loss, but fails in one case (out of 60). Our ML-based pipeline leads to phantoms that are significantly and substantially more individualized than currently used human-designed criteria.
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http://dx.doi.org/10.1117/1.JMI.7.4.046501 | DOI Listing |
Vet Res
January 2025
National and Regional Joint Engineering Laboratory for Medicament of Zoonoses Prevention and Control, Key Laboratory of Zoonoses, Ministry of Agriculture, Key Laboratory of Zoonoses Prevention and Control of Guangdong Province, Key Laboratory of Animal Vaccine Development, Ministry of Agriculture, College of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
S. Typhimurium is a significant zoonotic pathogen, and its survival and transmission rely on stress resistance and virulence factors. Therefore, identifying key regulatory elements is crucial for preventing and controlling S.
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January 2025
Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
Expression of CD2, CD25 and/or CD30 in extracutaneous mast cells (MC) is a minor diagnostic criterion for systemic mastocytosis (SM) in the classification of the World Health Organization and International Consensus Classification. So far, it remains unknown whether expression of these antigens on MC is of prognostic significance in SM. We performed a retrospective multi-center study of patients with SM using the data set of the registry of the European Competence Network on Mastocytosis, including 5034 patients with various MC disorders.
View Article and Find Full Text PDFJ Vet Med Sci
January 2025
Laboratory of Veterinary Surgery, Joint Faculty of Veterinary Medicine, Yamaguchi University.
A 9-year-old spayed female mixed breed dog weighing 6.8 kg with a history of previous splenectomy for hemangiosarcoma 4 years earlier was referred for a hepatic mass lesion. Although the dog did not have a clinical sign, a computed tomography revealed a solitary mass in the left medial lobe of the liver.
View Article and Find Full Text PDFFish Shellfish Immunol
January 2025
Guangdong Provincial Key Laboratory of Animal Molecular Design and Precise Breeding, School of Animal Science and Technology, Foshan University, Foshan, Guangdong 528225, China. Electronic address:
This study investigated the potential protective effect of AS-IV against heat stress-induced tissue damage in grass carp (Ctenopharyngodon idella). Grass carp were injected intraperitoneally with 0, 2, 4, and 8 mg/kg of AS-IV for three consecutive days, and then subjected to heat stress (35 ± 0.5°C); thereafter, histopathological analyses of the liver and spleen were performed at 0, 6, 24, and 48 h, respectively.
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