Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33150
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dc.contributor.authorTremblay, Samuel-
dc.contributor.authorAlhogbani, Mofarej-
dc.contributor.authorWeickhardt, Andrew J-
dc.contributor.authorDavis, Ian D-
dc.contributor.authorScott, Andrew M-
dc.contributor.authorHicks, Rodney J-
dc.contributor.authorMetser, Ur-
dc.contributor.authorChua, Sue-
dc.contributor.authorDavda, Reena-
dc.contributor.authorPunwani, Shonit-
dc.contributor.authorPayne, Heather-
dc.contributor.authorTunariu, Nina-
dc.contributor.authorHo, Bao-
dc.contributor.authorYoung, Sympascho-
dc.contributor.authorSingbo, Mahukpe Narcisse Ulrich-
dc.contributor.authorBauman, Glenn-
dc.contributor.authorEmmett, Louise-
dc.contributor.authorPouliot, Frédéric-
dc.date2023-
dc.date.accessioned2023-06-22T06:48:52Z-
dc.date.available2023-06-22T06:48:52Z-
dc.date.issued2023-06-08-
dc.identifier.citationCancer Imaging : the Official Publication of the International Cancer Imaging Society 2023-06-08; 23(1)en_US
dc.identifier.issn1470-7330-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33150-
dc.description.abstractThe impact of molecular imaging (MI) on patient management after biochemical recurrence (BCR) following radical prostatectomy has been described in many studies. However, it is not known if MI-induced management changes are appropriate. This study aimed to determine if androgen deprivation therapy (ADT) management plan is improved by MI in patients who are candidates for salvage radiation therapy. Data were analyzed from the multicenter prospective PROPS trial evaluating PSMA/Choline PET in patients being considered for salvage radiotherapy (sRT) with BCR after prostatectomy. We compared the pre- and post-MI ADT management plans for each patient and cancer outcomes as predicted by the MSKCC nomogram. A higher percentage of predicted BCR associated with ADT treatment intensification after MI was considered as an improvement in a patient's management. Seventy-three patients with a median PSA of 0.38 ng/mL were included. In bivariate analysis, a positive finding on MI (local or metastatic) was associated with decision to use ADT with an odds ratio of 3.67 (95% CI, 1.25 to 10.71; p = 0.02). No factor included in the nomogram was associated with decision to use ADT. Also, MI improved selection of patients to receive ADT based on predicted BCR after sRT : the predicted nomogram 5-year biochemical-free survivals were 52.5% and 43.3%, (mean difference, 9.2%; 95% CI 0.8 to 17.6; p = 0.03) for sRT alone and ADT±sRT subgroups, while there was no statistically significant difference between subgroups before MI. PSMA and/or Choline PET/CT before sRT can potentially improve patient ADT management by directing clinicians towards more appropriate intensification.en_US
dc.language.isoeng-
dc.subjectBiochemical recurrenceen_US
dc.subjectCholineen_US
dc.subjectMolecular imagingen_US
dc.subjectPSMAen_US
dc.subjectProstate canceren_US
dc.titleInfluence of molecular imaging on patient selection for treatment intensification prior to salvage radiation therapy for prostate cancer: a post hoc analysis of the PROPS trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleCancer Imaging : the Official Publication of the International Cancer Imaging Societyen_US
dc.identifier.affiliationCHU de Québec and Université Laval, Québec, Québec, Canada.en_US
dc.identifier.affiliationCHU de Québec and Université Laval, Québec, Québec, Canada.en_US
dc.identifier.affiliationLa Trobe University, Melbourne, Australia.en_US
dc.identifier.affiliationMonash University Eastern Health Clinical School, Box Hill, VIC, Australia.en_US
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationUniversity of Toronto, Toronto, ON, Canada.en_US
dc.identifier.affiliationRoyal Marsden Hospital, London, UK.en_US
dc.identifier.affiliationUniversity College London, London, UK.en_US
dc.identifier.affiliationSt. Vincent's Hospital, Sydney, NSW, Australia.en_US
dc.identifier.affiliationLondon Health Sciences Centre, London, ON, Canada.en_US
dc.identifier.affiliationRoyal Marsden Hospital, London, UK.en_US
dc.identifier.affiliationLondon Health Sciences Centre, London, ON, Canada.en_US
dc.identifier.affiliationCHU de Québec and Université Laval, Québec, Québec, Canada.en_US
dc.identifier.doi10.1186/s40644-023-00570-xen_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-6651-1079en_US
dc.identifier.pubmedid37291656-
dc.description.volume23-
dc.description.issue1-
dc.description.startpage57-
dc.subject.meshtermssecondaryProstatic Neoplasms/diagnostic imaging-
dc.subject.meshtermssecondaryProstatic Neoplasms/radiotherapy-
dc.subject.meshtermssecondaryPositron Emission Tomography Computed Tomography/methods-
dc.subject.meshtermssecondaryAndrogen Antagonists/therapeutic use-
dc.subject.meshtermssecondaryNeoplasm Recurrence, Local/pathology-
dc.subject.meshtermssecondaryProstatectomy/methods-
local.name.researcherScott, Andrew M
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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