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dc.contributor.authorCaillet, V
dc.contributor.authorKeall, P
dc.contributor.authorColvill, E
dc.contributor.authorHardcastle, N
dc.contributor.authorO'Brien, R
dc.contributor.authorSzymura, K
dc.contributor.authorBooth, JT
dc.date.accessioned2018-08-07
dc.date.available2018-08-07
dc.date.issued2017-07-01
dc.identifier.citationRadiother Oncol. 2017 Jul;124(1):18-24en
dc.identifier.urihttp://hdl.handle.net/2123/18638
dc.description.abstractPURPOSE: Assess the dosimetric impact of multi-leaf collimator (MLC) tracking and mid-ventilation (midV) planning compared with the internal target volume (ITV)-based planning approach for lung Stereotactic Ablative Body Radiotherapy (SABR). METHOD: Ten lung SABR patients originally treated with an ITV-based plan were re-planned according to MLC tracking and midV planning schemes. All plans were delivered on a linac to a motion phantom in a simulated treatment with real lung motions. Delivered dose was reconstructed in patient planning scans. ITV-based, tracking and midV regimes were compared at the planning and delivered stages based on PTV volume and dose metrics for the GTV and OAR. RESULTS: MLC tracking and midV schemes yielded favourable outcomes compared with ITV-based plans. Average reduction in PTV volume was (MLC tracking/MidV) 33.9%/22%. GTV dose coverage performed better with MLC tracking than the other regimes. Reduction in dose to OAR were for the lung (mean lung dose, 0.8Gy/0.2Gy), oesophagus (D3cc, 1.9Gy/1.4Gy), great vessels (D10cc, 3.2Gy/1.3Gy), trachea (D4cc, 1.1Gy/0.9Gy), heart (D1cc, 2.0Gy/0.5Gy) and spinal cord (D0.03cc, 0.5Gy/-0.1Gy). CONCLUSION: MLC tracking showed reduction in PTV volume, superior GTV dose coverage and organ dose sparing than MidV and ITV-based strategies.en
dc.publisherElsevieren
dc.relationNHMRC 1112096en
dc.rightsOther
dc.subjectMLC trackingen
dc.subjectLung tumouren
dc.titleMLC tracking for lung SABR reduces planning target volumes and dose to organs at risk.en
dc.typeArticleen
dc.subject.asrcFoR::029903 - Medical Physicsen
dc.identifier.doi10.1016/j.radonc.2017.06.016
dc.type.pubtypePreprinten
usyd.facultyFaculty of Medicine and Health, Sydney Medical Schoolen


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