Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/21744
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dc.contributor.authorOng, Wee Loon-
dc.contributor.authorKoh, Tze Lui-
dc.contributor.authorLim Joon, Daryl-
dc.contributor.authorChao, Michael-
dc.contributor.authorFarrugia, Briana-
dc.contributor.authorLau, Eddie-
dc.contributor.authorKhoo, Vincent-
dc.contributor.authorLawrentschuk, Nathan-
dc.contributor.authorBolton, Damien M-
dc.contributor.authorForoudi, Farshad-
dc.date2019-09-11-
dc.date.accessioned2019-09-16T04:32:24Z-
dc.date.available2019-09-16T04:32:24Z-
dc.date.issued2019-09-11-
dc.identifier.citationBJU International 2019; 124(Suppl 1): 19-30en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/21744-
dc.description.abstractTo report the outcomes of stereotactic ablative body radiotherapy (SABR) in men with oligometastatic prostate cancer (PCa) diagnosed on prostate-specific membrane antigen (PSMA)-positron emission tomography/computed tomography (PET/CT), based on a single-institution experience and the published literature. This was a retrospective cohort study of the first 20 consecutive men with oligometastatic PCa, treated with SABR in a single institution, who had biochemical recurrence after previous curative treatment (surgery/radiotherapy), had no evidence of local recurrence, were not on palliative androgen deprivation therapy (ADT), and had PSMA-PET/CT-confirmed oligometastatic disease (≤3 lesions). These men were treated with SABR to a dose of 30 Gy in three fractions for bone metastases, and 35-40 Gy in five fractions for nodal metastases. The outcomes of interest were: PSA response; local progression-free survival (LPFS); distant progression-free survival (DPFS); and ADT-free survival (ADTFS). A literature review was performed to identify published studies reporting on outcomes of PSMA-PET/CT-guided SABR. In our institutional cohort, 12 men (60%) had a decline in PSA post-SABR. One man had local progression 9.6 months post-SABR, with 12-month LPFS of 93%. Ten men had distant progression outside of their SABR treatment field, confirmed on PSMA-PET/CT, with 12-month DPFS of 62%, of whom four were treated with palliative ADT, two received prostate bed radiotherapy for prostate bed progression (confirmed on magnetic resonance imaging), and four received a further course of SABR (of whom one had further progression and was treated with palliative ADT). At last follow-up, six men (one with local progression and five with distant progression) had received palliative ADT. The 12-month ADTFS was 70%. Men with longer intervals between local curative treatment and SABR had better DPFS (P = 0.03) and ADTFS (P = 0.005). Four additional studies reporting on PSMA-PET/CT-guided SABR for oligometastatic PCa were identified and included in the review, giving a total of 346 patients. PSA decline was reported in 60-70% of men post-SABR. The 2-year LPFS, DPFS and ADTFS rates were 76-100%, 27-52%, and 58-62%, respectively. Our results showed that PSMA-PET/CT could have an important role in identifying men with true oligometastatic PCa who would benefit the most from metastases-directed therapy with SABR.en_US
dc.language.isoeng-
dc.subjectPSMA PETen_US
dc.subject#PCSMen_US
dc.subject#prostatecanceren_US
dc.subjectmetastatic directed treatmenten_US
dc.subjectoligometastasesen_US
dc.subjectProstate canceren_US
dc.subjectstereotactic radiotherapyen_US
dc.titleProstate-specific membrane antigen-positron emission tomography/computed tomography (PSMA-PET/CT)-guided stereotactic ablative body radiotherapy for oligometastatic prostate cancer: a single-institution experience and review of the published literature.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBJU Internationalen_US
dc.identifier.affiliationRadiologyen_US
dc.identifier.affiliationSchool of Clinical Medicine, University of Cambridge, Cambridge, UKen_US
dc.identifier.affiliationInstitute of Cancer Research, Royal Marsden NHS Foundation Trust, London, UKen_US
dc.identifier.affiliationDepartment of Medical Imaging and Radiation Sciences, Monash University, Clayton, Victoria, Australiaen_US
dc.identifier.affiliationEJ Whitten Prostate Cancer Research Centre, Epworth Healthcare, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationSurgeryen_US
dc.identifier.affiliationMolecular Imaging and Therapyen_US
dc.identifier.affiliationRadiation Oncologyen_US
dc.identifier.affiliationDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen_US
dc.identifier.doi10.1111/bju.14886en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-6657-7193en_US
dc.identifier.orcid0000-0002-1947-9694en_US
dc.identifier.orcid0000-0001-8553-5618en_US
dc.identifier.orcid0000-0002-5145-6783en_US
dc.identifier.orcid0000-0001-8387-0965en_US
dc.identifier.pubmedid31507035-
dc.type.austinJournal Article-
local.name.researcherBolton, Damien M
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptRadiation Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptRadiation Oncology-
crisitem.author.deptRadiation Oncology-
crisitem.author.deptRadiology-
crisitem.author.deptUrology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptRadiation Oncology-
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