Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/943
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dc.contributor.authorAckerly, Trevor-
dc.contributor.authorKenny, John-
dc.contributor.authorKnight, Richard-
dc.contributor.otherTaylor, Michael L.-
dc.contributor.otherKairn, Tanya-
dc.contributor.otherDunn, Leon-
dc.contributor.otherTrapp, Jamie-
dc.date2011-04-
dc.date.accessioned2016-12-05T03:30:11Z-
dc.date.available2016-12-05T03:30:11Z-
dc.date.issued2011-04-
dc.identifier.citationAustralas Phys Eng Sci Med (2011) 34: 105.en_US
dc.identifier.issn1879-5447en_US
dc.identifier.issn0158-9938en_US
dc.identifier.urihttp://hdl.handle.net/11434/943-
dc.descriptionConference Paper: Program EPSM-ABEC 2010 Conferenceen_US
dc.description.abstractCancers of the brain and central nervous system account for 1.6% of new cancers and 1.8% of cancer deaths globally. The highest rates of all developed nations are observed in Australia and New Zealand. There are known complexities associated with dose measurement of very small radiation fields. Here, 3D dosimetric verification of treatments for small intracranial tumours using gel dosimetry was investigated. An anthropomorphic head phantom with a 43 mm diameter and 63 mm long gel container was filled with PAGAT normoxic radiosensitive gel. In this work, we show results for a 12-field stereotactic radiotherapy treatment delivered using a Varian 21EX with BrainLAB mini-multi leaf collimator. The gel was read out using an Octopus-1Q laser optical CT scanner. Generally good agreement was observed between the measured doses and those calculated with the iPlan treatment planning system (pencil beam convolution); see Fig. I. For gamma criteria of 5%/5 mm the percentage of gamma values less than unity was 95% above the 80% isodose line, indicating good PTV coverage. For lower isodose regions approaching the boundaries of the container poorer agreement was observed. The feasibility of three-dimensional measurement of small field dose distributions in clinical contexts has been demonstrated. Development of this methodology has the potential to overcome many shortcomings of other dosimetric methods, such as limitations of spatial information (typically one- and two-dimensions), volume-averaging effects and perturbation due to poor mediamatching.en_US
dc.publisherSpringeren_US
dc.subjectPhysicsen_US
dc.subjectRadiotherapyen_US
dc.subjectX-Rayen_US
dc.subjectRadiographyen_US
dc.subjectDiagnostic Techniquesen_US
dc.subjectNuclear Medicineen_US
dc.subjectNeoplasmsen_US
dc.subjectCanceren_US
dc.subjectCarcinomasen_US
dc.subjectMaterials Testingen_US
dc.subjectDose Commitmentsen_US
dc.subjectDose Limitsen_US
dc.subjectSafety Standardsen_US
dc.subjectBrainen_US
dc.subjectCentral Nervous Systemen_US
dc.subjectIntracranial Tumoursen_US
dc.subjectEpworth Radiation Oncology Department, Epworth HealthCare, RIchmond, Victoria, Australia.en_US
dc.subjectCancer Services Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.titleThree-dimensional dose verification for clinical treatments of small intracranial tumours.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1007/s13246-011-0056-6en_US
dc.identifier.journaltitleAustralasian Physical and Engineering Sciences in Medicineen_US
dc.description.affiliatesRMIT University, Australiaen_US
dc.description.affiliatesThe Wesley Hospital, Australiaen_US
dc.description.affiliatesQueensland University, Australiaen_US
dc.description.affiliatesThe Alfred Hospital, Australiaen_US
dc.type.studyortrialClinical Trialen_US
dc.type.contenttypeTexten_US
Appears in Collections:Cancer Services
Radiation Oncology

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