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Spatiotemporal Fractionation in Radiotherapy

Torelli, Nathan

2024

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  • Título:
    Spatiotemporal Fractionation in Radiotherapy
  • Autor: Torelli, Nathan
  • Assuntos: Physics ; Physics Institute ; UZH Dissertations
  • Notas: Torelli, Nathan. Spatiotemporal Fractionation in Radiotherapy. 2024, University of Zurich, Faculty of Science.
    https://www.zora.uzh.ch/id/eprint/258699/
  • Descrição: In current clinical practice, radiotherapy treatments are often fractionated, i.e. the total radiation dose is equally divided into small fractions to be delivered daily over a period of few days or weeks. It has recently been shown in silico that spatiotemporal fractionation schemes, i.e. delivering distinct dose distributions in different fractions, can potentially improve the treatment. This is possible if these dose distributions are designed such that different fractions deliver similar doses to normal tissues (i.e. exploit the fractionation effect), but each fraction delivers high single-fraction doses to alternating parts of the tumor (i.e. achieve partial hypofractionation in the tumor). Thereby, the ratio of biological dose in the tumor versus the normal tissue can be improved. In this project, we further developed this innovative and novel concept. In particular, we focused on: 1. Developing new treatment planning algorithms for spatiotemporal fractionation 2. Identifying potential clinical applications of spatiotemporal fractionation with the aim of bringing spatiotemporal fractionation towards the design and implementation of a phase I clinical trial. Spatiotemporal fractionation is associated with higher complexity in treatment planning and delivery. Different plans with distinct dose distributions for different fractions must be designed such that all fractions together deliver the prescribed biological dose to the tumor. To that end, novel mathematical optimization methods for treatment planning have been developed, which are based on the cumulative biological dose rather than the physical dose. In particular, we developed robust treatment planning methods to account for geometric uncertainty in the patient setup and biological uncertainty in the fractionation sensitivity, which may lead to a degradation of the resulting treatment if not accounted for. It was shown that spatiotemporally fractionated treatments can be obtained which are robust against setup errors and uncertainty in the fractionation sensitivity. At the same time, these robust plans maintain most of their dosimetric benefit over uniformly fractionated plans. Besides liver cancer patients and patients with large arteriovenous malformations, patients with multiple brain metastases were identified to be especially well suited for spatiotemporal fractionation, because of the high accuracy in patient positioning. For theses patients, delivering high doses to different metastases in different fractions allows for fractionation of the normal brain dose in between the metastases while increasing the biological dose within the metastases. In addition, novel extensions of spatiotemporal fractionation were investigated. Spatiotemporal fractionation has been combined with other degrees of freedom that can be exploited in fractionated radiotherapy treatments, i.e. the combination of different particle types and treatment techniques, and the use of different beam orientations in different fractions. We showed that in the context of combined proton-photon therapy, spatiotemporal fractionation can be used to determine the optimal dose contribution of the proton and photon fractions to the tumor, thereby improving on simple proportional combination of intensity modulated radiotherapy and intensity modulated proton therapy plans. Also, we demonstrated that the quality of spatiotemporally fractionated treatments can be boosted by selecting fraction-specific beam orientations that are beneficial to treat specific regions of the tumor. To that end, a treatment planning algorithm was developed that allows for simultaneous optimization of multiple non-coplanar arc treatments. Finally, the simultaneous optimization of multiple dose distributions based on the cumulative biological dose is not supported by any commercial treatment planning system. To this end, we implemented a method which allows to import treatment plans optimized using our in-house research treatment planning system into a commercial treatment planning system. Thereby, it is possible to deliver spatiotemporally fractionated treatments in the clinics.
  • Data de criação/publicação: 2024
  • Idioma: Inglês

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