Biologically Targeted Radiation Therapy: Incorporating Patient-Specific Hypoxia Data Derived from Quantitative Magnetic Resonance Imaging.

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dc.contributor.author Her, Emily J
dc.contributor.author Haworth, Annette
dc.contributor.author Sun, Yu
dc.contributor.author Williams, Scott
dc.contributor.author Reynolds, Hayley M
dc.contributor.author Kennedy, Angel
dc.contributor.author Ebert, Martin A
dc.coverage.spatial Switzerland
dc.date.accessioned 2021-12-12T23:41:59Z
dc.date.available 2021-12-12T23:41:59Z
dc.date.issued 2021-9-29
dc.identifier.citation Cancers 13(19) 29 Sep 2021
dc.identifier.issn 2072-6694
dc.identifier.uri https://hdl.handle.net/2292/57744
dc.description.abstract <h4>Purpose</h4>Hypoxia has been linked to radioresistance. Strategies to safely dose escalate dominant intraprostatic lesions have shown promising results, but further dose escalation to overcome the effects of hypoxia require a novel approach to constrain the dose in normal tissue.to safe levels. In this study, we demonstrate a biologically targeted radiotherapy (BiRT) approach that can utilise multiparametric magnetic resonance imaging (mpMRI) to target hypoxia for favourable treatment outcomes.<h4>Methods</h4>mpMRI-derived tumour biology maps, developed via a radiogenomics study, were used to generate individualised, hypoxia-targeting prostate IMRT plans using an ultra- hypofractionation schedule. The spatial distribution of mpMRI textural features associated with hypoxia-related genetic profiles was used as a surrogate of tumour hypoxia. The effectiveness of the proposed approach was assessed by quantifying the potential benefit of a general focal boost approach on tumour control probability, and also by comparing the dose to organs at risk (OARs) with hypoxia-guided focal dose escalation (DE) plans generated for five patients.<h4>Results</h4>Applying an appropriately guided focal boost can greatly mitigate the impact of hypoxia. Statistically significant reductions in rectal and bladder dose were observed for hypoxia-targeting, biologically optimised plans compared to isoeffective focal DE plans.<h4>Conclusion</h4>Results of this study suggest the use of mpMRI for voxel-level targeting of hypoxia, along with biological optimisation, can provide a mechanism for guiding focal DE that is considerably more efficient than application of a general, dose-based optimisation, focal boost.
dc.format.medium Electronic
dc.language eng
dc.publisher MDPI AG
dc.relation.ispartofseries Cancers
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject hypoxia
dc.subject multiparametric MRI
dc.subject prostate cancer
dc.subject radiogenomics
dc.subject tumour control probability
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Oncology
dc.subject prostate cancer
dc.subject hypoxia
dc.subject tumour control probability
dc.subject radiogenomics
dc.subject multiparametric MRI
dc.subject PROSTATE-CANCER
dc.subject ALPHA/BETA RATIO
dc.subject RADIOTHERAPY
dc.subject OPTIMIZATION
dc.subject CELLS
dc.subject REOXYGENATION
dc.subject INTERMEDIATE
dc.subject IRRADIATION
dc.subject IMPLANTS
dc.subject PROMOTES
dc.subject 1112 Oncology and Carcinogenesis
dc.title Biologically Targeted Radiation Therapy: Incorporating Patient-Specific Hypoxia Data Derived from Quantitative Magnetic Resonance Imaging.
dc.type Journal Article
dc.identifier.doi 10.3390/cancers13194897
pubs.issue 19
pubs.begin-page 4897
pubs.volume 13
dc.date.updated 2021-11-14T07:56:15Z
dc.rights.holder Copyright: The author en
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/34638382
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype research-article
pubs.subtype Journal Article
pubs.elements-id 869027
dc.identifier.eissn 2072-6694
dc.identifier.pii cancers13194897
pubs.number ARTN 4897
pubs.online-publication-date 2021-9-29


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