Detecting localised prostate cancer using radiomic features in PSMA PET and multiparametric MRI for biologically targeted radiation therapy

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dc.contributor.author Chan, Tsz Him
dc.contributor.author Haworth, Annette
dc.contributor.author Wang, Alan
dc.contributor.author Osanlouy, Mahyar
dc.contributor.author Williams, Scott
dc.contributor.author Mitchell, Catherine
dc.contributor.author Hofman, Michael S
dc.contributor.author Hicks, Rodney J
dc.contributor.author Murphy, Declan G
dc.contributor.author Reynolds, Hayley M
dc.coverage.spatial Germany
dc.date.accessioned 2023-10-06T00:38:05Z
dc.date.available 2023-10-06T00:38:05Z
dc.date.issued 2023-04
dc.identifier.citation (2023). EJNMMI Research, 13(1), 34-.
dc.identifier.issn 2191-219X
dc.identifier.uri https://hdl.handle.net/2292/66173
dc.description.abstract Background Prostate-Specifc Membrane Antigen (PSMA) PET/CT and multiparametric MRI (mpMRI) are wellestablished modalities for identifying intra-prostatic lesions (IPLs) in localised prostate cancer. This study aimed to investigate the use of PSMA PET/CT and mpMRI for biologically targeted radiation therapy treatment planning by: (1) analysing the relationship between imaging parameters at a voxel-wise level and (2) assessing the performance of radiomic-based machine learning models to predict tumour location and grade. Methods PSMA PET/CT and mpMRI data from 19 prostate cancer patients were co-registered with whole-mount histopathology using an established registration framework. Apparent Difusion Coefcient (ADC) maps were computed from DWI and semi-quantitative and quantitative parameters from DCE MRI. Voxel-wise correlation analysis was conducted between mpMRI parameters and PET Standardised Uptake Value (SUV) for all tumour voxels. Classifcation models were built using radiomic and clinical features to predict IPLs at a voxel level and then classifed further into high-grade or low-grade voxels. Results Perfusion parameters from DCE MRI were more highly correlated with PET SUV than ADC or T2w. IPLs were best detected with a Random Forest Classifer using radiomic features from PET and mpMRI rather than either modality alone (sensitivity, specifcity and area under the curve of 0.842, 0.804 and 0.890, respectively). The tumour grading model had an overall accuracy ranging from 0.671 to 0.992. Conclusions Machine learning classifers using radiomic features from PSMA PET and mpMRI show promise for predicting IPLs and diferentiating between high-grade and low-grade disease, which could be used to inform biologically targeted radiation therapy planning.
dc.format.medium Electronic
dc.language eng
dc.publisher Springer Nature
dc.relation.ispartofseries EJNMMI research
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 Multiparametric MRI
dc.subject PSMA PET/CT
dc.subject Prostate cancer
dc.subject Radiation therapy
dc.subject Radiomics
dc.subject 32 Biomedical and Clinical Sciences
dc.subject 3202 Clinical Sciences
dc.subject 3211 Oncology and Carcinogenesis
dc.subject Cancer
dc.subject Urologic Diseases
dc.subject Bioengineering
dc.subject Aging
dc.subject Biomedical Imaging
dc.subject 4 Detection, screening and diagnosis
dc.subject 4.4 Population screening
dc.subject 4.2 Evaluation of markers and technologies
dc.subject 3 Good Health and Well Being
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Radiology, Nuclear Medicine & Medical Imaging
dc.subject PSMA PET
dc.subject CT
dc.subject POSITRON-EMISSION-TOMOGRAPHY
dc.subject DIAGNOSIS
dc.subject SYSTEM
dc.subject 1101 Medical Biochemistry and Metabolomics
dc.subject 1103 Clinical Sciences
dc.subject 1112 Oncology and Carcinogenesis
dc.title Detecting localised prostate cancer using radiomic features in PSMA PET and multiparametric MRI for biologically targeted radiation therapy
dc.type Journal Article
dc.identifier.doi 10.1186/s13550-023-00984-5
pubs.issue 1
pubs.begin-page 34
pubs.volume 13
dc.date.updated 2023-09-04T03:50:26Z
dc.rights.holder Copyright: The authors en
dc.identifier.pmid 37099047 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/37099047
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 959002
pubs.org-id Bioengineering Institute
dc.identifier.eissn 2191-219X
dc.identifier.pii 10.1186/s13550-023-00984-5
pubs.number 34
pubs.record-created-at-source-date 2023-09-04
pubs.online-publication-date 2023-04-26


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