On-line MR imaging for dose validation of abdominal radiotherapy
DENIS DE SENNEVILLE, Baudouin
University Medical Center [Utrecht] [UMCU]
Institut de Mathématiques de Bordeaux [IMB]
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University Medical Center [Utrecht] [UMCU]
Institut de Mathématiques de Bordeaux [IMB]
DENIS DE SENNEVILLE, Baudouin
University Medical Center [Utrecht] [UMCU]
Institut de Mathématiques de Bordeaux [IMB]
< Réduire
University Medical Center [Utrecht] [UMCU]
Institut de Mathématiques de Bordeaux [IMB]
Langue
en
Article de revue
Ce document a été publié dans
Physics in Medicine and Biology. 2015
IOP Publishing
Résumé en anglais
For quality assurance and adaptive radiotherapy, validation of the actual delivered dose is crucial.Intrafractional anatomy changes cannot be captured satisfactorily during treatment with hitherto available imaging ...Lire la suite >
For quality assurance and adaptive radiotherapy, validation of the actual delivered dose is crucial.Intrafractional anatomy changes cannot be captured satisfactorily during treatment with hitherto available imaging modalitites. Consequently, dosecalculations are based on the assumption of static anatomy throughout the treatment. However, intra- and interfraction anatomy is dynamic and changes can be significant. In particular, hypofractionated and escalated radiotherapy thus demand for reliable dose reconstruction based on periodic imaging.In this paper, we investigate the use of an MR -linac as a dose tracking modality for the validation of treatments in abdominal targets where both respiratory and long-term peristaltic and drift motion occurs.The on-line MR imaging capabilities of the modality provides the means to perform respiratory gating of both delivery and acquisition yielding a model-free respiratory motion management under free breathing conditions.In parallel to the treatment, the volumetric patient anatomy was captured and used to calculate the applied dose. Subsequently, the individual doses were warped back to the planing grid to obtain the actual dose accumulated over the entire treatment duration. Eventually, the planned dose was validated by comparison with the accumulated dose.Representatively for a site subject to breathing modulation, two kidney cases (25Gy target dose) demonstrated the working principle on volunteer data and simulated delivery. The proposed workflow successfully showed its ability to track local dosimetric changes. Integration of the on-line anatomy information could reveal local dose variations −2.3 to 1.5Gy in the target volume of a volunteer dataset. In the adjacent organs at risk, high local dose errors ranging from −2.5 to 1.9Gy could be traced back.< Réduire
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