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dc.contributor.authorMadden, Levi
dc.contributor.authorAhmed, Abdella
dc.contributor.authorStewart, Maegan
dc.contributor.authorChrystall, Danielle
dc.contributor.authorMylonas, Adam
dc.contributor.authorBrown, Ryan
dc.contributor.authorNguyen, Doan Trang
dc.contributor.authorKeall, Paul
dc.contributor.authorBooth, Jeremy
dc.date.accessioned2024-09-20T02:41:04Z
dc.date.available2024-09-20T02:41:04Z
dc.date.issued2024en_AU
dc.identifier.urihttps://hdl.handle.net/2123/33098
dc.description.abstractObjective.In current radiograph-based intra-fraction markerless target-tracking, digitally reconstructed radiographs (DRRs) from planning CTs (CT-DRRs) are often used to train deep learning models that extract information from the intra-fraction radiographs acquired during treatment. Traditional DRR algorithms were designed for patient alignment (i.e.bone matching) and may not replicate the radiographic image quality of intra-fraction radiographs at treatment. Hypothetically, generating DRRs from pre-treatment Cone-Beam CTs (CBCT-DRRs) with DRR algorithms incorporating physical modelling of on-board-imagers (OBIs) could improve the similarity between intra-fraction radiographs and DRRs by eliminating inter-fraction variation and reducing image-quality mismatches between radiographs and DRRs. In this study, we test the two hypotheses that intra-fraction radiographs are more similar to CBCT-DRRs than CT-DRRs, and that intra-fraction radiographs are more similar to DRRs from algorithms incorporating physical models of OBI components than DRRs from algorithms omitting these models.Approach.DRRs were generated from CBCT and CT image sets collected from 20 patients undergoing pancreas stereotactic body radiotherapy. CBCT-DRRs and CT-DRRs were generated replicating the treatment position of patients and the OBI geometry during intra-fraction radiograph acquisition. To investigate whether the modelling of physical OBI components influenced radiograph-DRR similarity, four DRR algorithms were applied for the generation of CBCT-DRRs and CT-DRRs, incorporating and omitting different combinations of OBI component models. The four DRR algorithms were: a traditional DRR algorithm, a DRR algorithm with source-spectrum modelling, a DRR algorithm with source-spectrum and detector modelling, and a DRR algorithm with source-spectrum, detector and patient material modelling. Similarity between radiographs and matched DRRs was quantified using Pearson's correlation and Czekanowski's index, calculated on a per-image basis. Distributions of correlations and indexes were compared to test each of the hypotheses. Distribution differences were determined to be statistically significant when Wilcoxon's signed rank test and the Kolmogorov-Smirnov two sample test returnedp≤ 0.05 for both tests.Main results.Intra-fraction radiographs were more similar to CBCT-DRRs than CT-DRRs for both metrics across all algorithms, with allp≤ 0.007. Source-spectrum modelling improved radiograph-DRR similarity for both metrics, with allp< 10-6. OBI detector modelling and patient material modelling did not influence radiograph-DRR similarity for either metric.Significance.Generating DRRs from pre-treatment CBCT-DRRs is feasible, and incorporating CBCT-DRRs into markerless target-tracking methods may promote improved target-tracking accuracies. Incorporating source-spectrum modelling into a treatment planning system's DRR algorithms may reinforce the safe treatment of cancer patients by aiding in patient alignment.en_AU
dc.language.isoenen_AU
dc.publisherIOP Sciencesen_AU
dc.relation.ispartofBiomedical Physics & Engineering Expressen_AU
dc.rightsCreative Commons Attribution 4.0en_AU
dc.subjectMedical Imagingen_AU
dc.subjectpancreatic canceren_AU
dc.subjectradiation therapyen_AU
dc.titleCBCT-DRRs superior to CT-DRRs for target-tracking applications during pancreatic SBRTen_AU
dc.typeArticleen_AU
dc.subject.asrcANZSRC FoR code::32 BIOMEDICAL AND CLINICAL SCIENCES::3211 Oncology and carcinogenesis::321110 Radiation therapyen_AU
dc.identifier.doi10.1088/2057-1976/ad3bb9
dc.type.pubtypeAuthor accepted manuscripten_AU
dc.relation.arc2019TPG2165
dc.relation.nhmrc1194004
usyd.facultySeS faculties schools::Faculty of Medicine and Healthen_AU
usyd.departmentImage X Instituteen_AU
usyd.citation.volume10en_AU
usyd.citation.issue3en_AU
usyd.citation.spage035039en_AU
workflow.metadata.onlyNoen_AU


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