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dc.contributor.authorDean, JA
dc.contributor.authorWelsh, LC
dc.contributor.authorMcQuaid, D
dc.contributor.authorWong, KH
dc.contributor.authorAleksic, A
dc.contributor.authorDunne, E
dc.contributor.authorIslam, MR
dc.contributor.authorPatel, A
dc.contributor.authorPatel, P
dc.contributor.authorPetkar, I
dc.contributor.authorPhillips, I
dc.contributor.authorSham, J
dc.contributor.authorNewbold, KL
dc.contributor.authorBhide, SA
dc.contributor.authorHarrington, KJ
dc.contributor.authorGulliford, SL
dc.contributor.authorNutting, CM
dc.date.accessioned2016-08-26T15:22:20Z
dc.date.issued2016-04-01
dc.identifier.citationRadiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology, 2016, 119 (1), pp. 166 - 171
dc.identifier.issn0167-8140
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/79
dc.identifier.eissn1879-0887
dc.identifier.doi10.1016/j.radonc.2016.02.022
dc.description.abstractBACKGROUND AND PURPOSE: Current oral mucositis normal tissue complication probability models, based on the dose distribution to the oral cavity volume, have suboptimal predictive power. Improving the delineation of the oral mucosa is likely to improve these models, but is resource intensive. We developed and evaluated fully-automated atlas-based segmentation (ABS) of a novel delineation technique for the oral mucosal surfaces. MATERIAL AND METHODS: An atlas of mucosal surface contours (MSC) consisting of 46 patients was developed. It was applied to an independent test cohort of 10 patients for whom manual segmentation of MSC structures, by three different clinicians, and conventional outlining of oral cavity contours (OCC), by an additional clinician, were also performed. Geometric comparisons were made using the dice similarity coefficient (DSC), validation index (VI) and Hausdorff distance (HD). Dosimetric comparisons were carried out using dose-volume histograms. RESULTS: The median difference, in the DSC and HD, between automated-manual comparisons and manual-manual comparisons were small and non-significant (-0.024; p=0.33 and -0.5; p=0.88, respectively). The median VI was 0.086. The maximum normalised volume difference between automated and manual MSC structures across all of the dose levels, averaged over the test cohort, was 8%. This difference reached approximately 28% when comparing automated MSC and OCC structures. CONCLUSIONS: Fully-automated ABS of MSC is suitable for use in radiotherapy dose-response modelling.
dc.formatPrint-Electronic
dc.format.extent166 - 171
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER IRELAND LTD
dc.subjectMouth Mucosa
dc.subjectHumans
dc.subjectHead and Neck Neoplasms
dc.subjectRadiotherapy Dosage
dc.subjectRadiometry
dc.subjectDose-Response Relationship, Radiation
dc.subjectAtlases as Topic
dc.subjectOrgans at Risk
dc.titleAssessment of fully-automated atlas-based segmentation of novel oral mucosal surface organ-at-risk.
dc.typeJournal Article
dcterms.dateAccepted2016-02-09
rioxxterms.versionofrecord10.1016/j.radonc.2016.02.022
rioxxterms.licenseref.startdate2016-04
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfRadiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
pubs.issue1
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Horwich)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Radiotherapy Physics Modelling
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Clinical Academic Radiotherapy (Horwich)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Radiotherapy Physics Modelling
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.publication-statusPublished
pubs.volume119
pubs.embargo.termsNo embargo
icr.researchteamClinical Academic Radiotherapy (Horwich)
icr.researchteamRadiotherapy Physics Modelling
icr.researchteamTargeted Therapy
dc.contributor.icrauthorDean, Jamie
dc.contributor.icrauthorPatel, Priyanka
dc.contributor.icrauthorHarrington, Kevin


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