Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22004
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dc.contributor.authorEmmett, Louise-
dc.contributor.authorTang, Reuben-
dc.contributor.authorNandurkar, Rohan H-
dc.contributor.authorHruby, George-
dc.contributor.authorRoach, Paul J-
dc.contributor.authorWatts, Jo Anne-
dc.contributor.authorCusick, Thomas-
dc.contributor.authorKneebone, Andrew-
dc.contributor.authorHo, Bao-
dc.contributor.authorChan, Lyn-
dc.contributor.authorvan Leeuwen, Pim-
dc.contributor.authorScheltema, Matthijs-
dc.contributor.authorNguyen, Andrew-
dc.contributor.authorYin, Charlotte-
dc.contributor.authorScott, Andrew M-
dc.contributor.authorTang, Colin-
dc.contributor.authorMcCarthy, Michael-
dc.contributor.authorFullard, Karen-
dc.contributor.authorRoberts, Matthew-
dc.contributor.authorFrancis, Roslyn-
dc.contributor.authorStricker, Phillip-
dc.date2019-11-01-
dc.date.accessioned2019-11-06T04:04:37Z-
dc.date.available2019-11-06T04:04:37Z-
dc.date.issued2019-11-01-
dc.identifier.citationJournal of nuclear medicine : official publication, Society of Nuclear Medicine 2019; online first: 1 November-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22004-
dc.description.abstractBackground:68Ga PSMA PET CT (PSMA) is increasingly used in men with biochemical recurrence (BCR) post radical prostatectomy (RP), but its longer term prognostic / predictive potential in these men is unknown. The aim of this study was to evaluate the predictive value of PSMA PET for 3 year freedom from progression (FFP) in men with BCR post RP undergoing salvage radiotherapy (sRT). Methods: This prospective multi-center study enrolled 260 men between 2015 and 2017. Eligible patients were referred for PSMA with rising PSA following RP. Management following PSMA was recorded but not mandated. PSMA protocols were standardised across sites and reported prospectively. Clinical, pathological and surgical information, sRT, timing and duration of androgen deprivation (ADT), 3 year PSA results and clinical events were documented. FFP was defined as a PSA rise ≤ 0.2ng/mL above nadir post sRT, with no additional treatment. Results: The median PSA was 0.26ng/mL (IQR 0.15 - 0.59) and follow-up 38 months (IQR 31-43). PSMA was negative in 34.6% (90/260), confined to prostate fossa 21.5% (56/260), pelvic nodes 26.2% (68/260), and distant disease 17.7% (46/260). 71.5% (186/260) received sRT, 38.2% (71/186) to the fossa only, 49.4% (92/186) fossa + pelvic nodes and 12.4% (23/186) nodes alone/SBRT. PSMA was highly predictive of FFP at 3 years following sRT. Overall, FFP was achieved in 64.5% (120/186) of those who received sRT, 81% (81/100) with negative/fossa confined vs. 45% (39/86) for extra fossa disease (p<0.0001). On logistic regression PSMA was more independently predictive of FFP than established clinical predictors, including PSA, T-stage, surgical margin status or Gleason score (P < 0.002). 32% of men with a negative PSMA PET did not receive treatment. Of these, 66% (19/29) progressed, with a mean rise in PSA of 1.59ng/mL over the 3 years. Conclusion: PSMA PET result is highly predictive of FFP at 3 years in men undergoing sRT for BCR following RP. In particular, men with negative PSMA PET or disease identified as still confined to the prostate fossa demonstrate high FFP, despite receiving less extensive radiotherapy and lower rates of additional ADT than those with extra fossa disease.-
dc.language.isoeng-
dc.subjectOncology: GU-
dc.subjectPET CT-
dc.subjectPET/CT-
dc.subjectPeptides-
dc.subjectProstate specific membrane antigen-
dc.subjectRadiation Therapy Planning-
dc.subjectbiochemical failure-
dc.subjectpost radical prostatectomy-
dc.subjecttreatment outcome-
dc.title3-year freedom from progression following 68GaPSMA PET CT triaged management in men with biochemical recurrence post radical prostatectomy. Results of a prospective multi-center trial.-
dc.typeJournal Article-
dc.identifier.journaltitleJournal of nuclear medicine : official publication, Society of Nuclear Medicine-
dc.identifier.affiliationDepartment of Urology, The Netherlands Cancer Institute, Netherlandsen
dc.identifier.affiliationDepartment of Nuclear Medicine/WA PET Services, Sir Charles Gairdner Hospital, Australiaen
dc.identifier.affiliationGarvan Institute of Medical Research and & The Kinghorn Cancer Centreen
dc.identifier.affiliationFaculty of Medicine, University of New South Wales, Australiaen
dc.identifier.affiliationFaculty of Health and Medical Science, University of Western Australia, Australiaen
dc.identifier.affiliationFaculty of Medicine, University of Queensland, Australiaen
dc.identifier.affiliationDepartment of Nuclear Medicine and Theranostics, St Vincent's Hospital, Australiaen
dc.identifier.affiliationDepartment of Nuclear Medicine, Fiona Stanley Hospital, Australiaen
dc.identifier.affiliationDepartment of Radiation Oncology, Sir Charles Gairdner Hospital, Australiaen
dc.identifier.affiliationDepartment of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Nuclear Medicine, Royal North Shore Hospital, Australiaen
dc.identifier.affiliationDepartment of Radiation Oncology, Royal North Shore Hospital, Australiaen
dc.identifier.doi10.2967/jnumed.119.235028-
dc.identifier.orcidDepartment of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia-
dc.identifier.pubmedid31676727-
dc.type.austinJournal Article-
local.name.researcherScott, Andrew M
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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