Modelling Tumour Control in External Beam Radiotherapy for Prostate Cancer

atmire.migration.oldid3716
dc.contributor.advisorKirkby, Charles
dc.contributor.authorBalderson, Michael
dc.date.accessioned2015-09-30T21:06:24Z
dc.date.available2015-11-20T08:00:44Z
dc.date.issued2015-09-30
dc.date.submitted2015en
dc.description.abstractModeling tumour control for prostate treatments can be challenging. Models used to predict tumour control are typically based on the well known linear-quadratic (LQ) model for cell survival. The LQ model accurately predicts cell killing for a given radiation dose in most cases, however in some cases the LQ model falls short and LQ model predictions differ from what has been observed experimentally. Cell survival following low radiation doses <1Gy and radiation induced bystander effects are two examples where the LQ model potentially falls short at modelling cell survival following an absorbed radiation dose. Using mathematical models that account for radiation induced bystander and low dose hypersensitivity effects, we look at how these effects potentially change predicted outcomes of tumour control when compared to standard LQ predictions. We start by investigating how the basic LQ model predicts tumour control under large geometric miss errors under intensity modulated radiation therapy (IMRT) and volume modulated arc therapy (VMAT) modalities. Next, we look at the geometric miss scenario again, but rather than compare two different delivery techniques we investigate how radiation induced bystander effects potentially change predicted tumour control under geometric miss cases. We then expand on this idea and study how radiation induced bystander effects potentially influence predicted outcome under heterogeneous dose distributions. Finally, we compare the relative biological effectiveness (RBE) of bystander effects with low dose hypersensitivity effects and spectral effects for out-of-field radiation doses. The majority of this work focused on how radiation induced bystander effect changed biological modeling of tumour control in external beam radiotherapy for prostate cancer. This work ultimately demonstrates that bystander effects can modify predicted outcomes of tumour control. We have shown that bystander effects potentially improve TCP under geometric miss and that bystander effects may relax the common planning constraint of aiming for dose homogeneity within a target volume.en_US
dc.identifier.citationBalderson, M. (2015). Modelling Tumour Control in External Beam Radiotherapy for Prostate Cancer (Doctoral thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/26965en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/26965
dc.identifier.urihttp://hdl.handle.net/11023/2575
dc.language.isoeng
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectBiology--Cell
dc.subjectBiophysics
dc.subjectPhysics
dc.subject.classificationBystanderen_US
dc.titleModelling Tumour Control in External Beam Radiotherapy for Prostate Cancer
dc.typedoctoral thesis
thesis.degree.disciplinePhysics and Astronomy
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameDoctor of Philosophy (PhD)
ucalgary.item.requestcopytrue
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