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dc.contributor.authorBohsung, J
dc.contributor.authorGillis, Sofie
dc.contributor.authorArrans, Rafael
dc.contributor.authorBakai, Annemarie
dc.contributor.authorDe Wagter, Carlos
dc.contributor.authorKnöös, Tommy
dc.contributor.authorMijnheer, Ben J
dc.contributor.authorPaiusco, Marta
dc.contributor.authorPerrin, Bruce A
dc.contributor.authorWelleweerd, Hans
dc.contributor.authorWilliams, Peter C
dc.date.accessioned2009-08-05T12:16:24Z
dc.date.available2009-08-05T12:16:24Z
dc.date.issued2005-09
dc.identifier.citationIMRT treatment planning:- a comparative inter-system and inter-centre planning exercise of the ESTRO QUASIMODO group. 2005, 76 (3):354-61 Radiother Oncolen
dc.identifier.issn0167-8140
dc.identifier.pmid16154218
dc.identifier.doi10.1016/j.radonc.2005.08.003
dc.identifier.urihttp://hdl.handle.net/10541/76332
dc.description.abstractBACKGROUND AND PURPOSE: The purpose of this work was a comparison of realistic IMRT plans based on the same CT-image data set and a common predefined set of dose objectives for the planning target volume and the organs at risk. This work was part of the larger European QUASIMODO IMRT verification project. MATERIALS AND METHODS: Eleven IMRT plans were produced by nine different European groups, each applying a representative set of clinically used IMRT treatment planning systems. The plans produced were to be deliverable in a clinically acceptable treatment time with the local technical equipment. All plans were characterized using a set of different quality measures such as dose-volume histograms, number of monitor units and treatment time. RESULTS: Only one plan was able to fulfil all dose objectives strictly; six plans failed some of the objectives but were still considered to be clinically acceptable; four plans were not able to reach the objectives. Additional quality scores such as the number of monitor units and treatment time showed large variations, which mainly depend on the delivery technique. CONCLUSION: The presented planning study showed that with nearly all presently available IMRT planning and delivery systems comparable dose distributions could be achieved if the planning goals are clearly defined in advance.
dc.language.isoenen
dc.subjectCanceren
dc.subject.meshAnthropometry
dc.subject.meshDose Fractionation
dc.subject.meshEurope
dc.subject.meshHumans
dc.subject.meshNeoplasms
dc.subject.meshQuality Assurance, Health Care
dc.subject.meshRadiometry
dc.subject.meshRadiotherapy
dc.subject.meshReproducibility of Results
dc.titleIMRT treatment planning:- a comparative inter-system and inter-centre planning exercise of the ESTRO QUASIMODO group.en
dc.typeArticleen
dc.contributor.departmentDepartment of Radiotherapy, Charité Campus Mitte, Berlin, Germany. joerg.bohsung@charite.deen
dc.identifier.journalRadiotherapy and Oncologyen
html.description.abstractBACKGROUND AND PURPOSE: The purpose of this work was a comparison of realistic IMRT plans based on the same CT-image data set and a common predefined set of dose objectives for the planning target volume and the organs at risk. This work was part of the larger European QUASIMODO IMRT verification project. MATERIALS AND METHODS: Eleven IMRT plans were produced by nine different European groups, each applying a representative set of clinically used IMRT treatment planning systems. The plans produced were to be deliverable in a clinically acceptable treatment time with the local technical equipment. All plans were characterized using a set of different quality measures such as dose-volume histograms, number of monitor units and treatment time. RESULTS: Only one plan was able to fulfil all dose objectives strictly; six plans failed some of the objectives but were still considered to be clinically acceptable; four plans were not able to reach the objectives. Additional quality scores such as the number of monitor units and treatment time showed large variations, which mainly depend on the delivery technique. CONCLUSION: The presented planning study showed that with nearly all presently available IMRT planning and delivery systems comparable dose distributions could be achieved if the planning goals are clearly defined in advance.


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