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dc.contributorFaculty of Health and Social Sciencesen_US
dc.contributor.advisorCai, Jing (HTI)en_US
dc.creatorWong, Tsz Lung-
dc.identifier.urihttps://theses.lib.polyu.edu.hk/handle/200/12851-
dc.languageEnglishen_US
dc.publisherHong Kong Polytechnic Universityen_US
dc.rightsAll rights reserveden_US
dc.titleBiochemical Prostate Specific Antigen (PSA) prediction for prostate cancer patients receiving MR-guided radiotherapy using multi-modality radiomicsen_US
dcterms.abstractIntroductionen_US
dcterms.abstractPrediction of early treatment response in prostate cancer is highly acclaimed and important for treatment decision making. However, there is a lack of prediction strategy applied in current clinical practice. This retrospective study will predict one-month post-treatment serum PSA level as a surrogate of early treatment response for prostate cancer patient treated with SBRT via pre-treatment CT and MR images using radiomics approaches.en_US
dcterms.abstractMethodsen_US
dcterms.abstractOne hundred and nine prostate cancer patients receiving 5 fractions of Stereotactic Body Radiotherapy (SBRT) in Elekta Unity MR-Linac at Hong Kong Sanatorium Hospital Eastern Cancer Centre from Jan 2020 to May 2021 were retrospectively recruited into the study. Pre-treatment CT and T2-w MR images were processed using RADAR (software developed in-house by Department of Health, Technology and Information at Hong Kong Polytechnic University). 1130 radiomics features were extracted from the prostate CTV (clinical target volume) in CT and MR images. The radiomic model was trained using CT and MR-based radiomic features to predict the serum PSA status one month after the completion of treatment. The maximum relevance and minimum redundancy (mRMR) feature selection algorithm was implemented to select the final features for the radiomic model building. The performance of the radiomic model was validated using a 3-fold cross-validation. Area under the receiver operating characteristic curve (AUC of ROC) for the cross-validation were used to evaluate the predictive power of the radiomic model.en_US
dcterms.abstractResultsen_US
dcterms.abstractHighest 8 features from CT were selected to build the CT-model and highest 8 features from MR to build the MR-model. Averaged AUC in training and testing over cross-validations were 0.83 (SD=0.04) and 0.77 (SD=0.08) for CT-based radiomic model. For MR-based model, the AUC for training and testing were 0.85 (SD=0.04) and 0.78 (SD=0.09) respectively. The statistical test showed there is no significant AUC difference in CT vs. MR-based radiomic model (p > 0.05). The combined model (CT + MR) without re-prioritizing both radiomics features using CT (n=6) and MR (n=6) showed AUC of 0.89 (SD=0.02) and 0.82 (SD=0.09) for training and testing respectively. The statistical test demonstrated a statistically significant improvement (p<0.05) when compared to CT alone model but not with MR alone model in response prediction. The model (CTMR) using a hybrid and mRMR re-prioritized features from both modalities with 11 shortlisted features (CT=6, MR=5) demonstrated AUC of 0.90 (SD=0.03) and 0.83 (SD=0.09) in training and testing respectively. When comparing the AUC with CT or MR alone model, the statistical test showed the result is significant (p>0.05) in both tests.en_US
dcterms.abstractConclusionen_US
dcterms.abstractThe results indicate radiomics features from CT & MR have the potential to predict the change of one-month post-treatment serum PSA level for prostate cancer. And the combined model (CTMR) using mRMR to re-prioritizes the combined features achieve the best AUC of ROC curve when compared with other models (p<0.05). Our results demonstrated multi-modality CT & MR radiomics can successfully predict early PSA results after SBRT in prostate cancer patients. And the prediction power in hybrid model is more superior than single modality models. The potential application of the results in clinical environment could assist the clinician in practicing precision medicine based on multi-modality radiomics model prediction.en_US
dcterms.extentxx, 106 pages : color illustrationsen_US
dcterms.isPartOfPolyU Electronic Thesesen_US
dcterms.issued2023en_US
dcterms.educationalLevelDHScen_US
dcterms.educationalLevelAll Doctorateen_US
dcterms.LCSHProstate -- Cancer -- Diagnosisen_US
dcterms.LCSHProstate -- Cancer -- Prognosisen_US
dcterms.LCSHProstate -- Cancer -- Treatmenten_US
dcterms.LCSHDiagnostic imagingen_US
dcterms.LCSHHong Kong Polytechnic University -- Dissertationsen_US
dcterms.accessRightsrestricted accessen_US

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