Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/2064
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dc.contributor.authorMoon, Daniel-
dc.contributor.authorMurphy, Declan-
dc.contributor.otherEmmett, Louise-
dc.contributor.otherPapa, Nathan-
dc.contributor.otherButeau, James-
dc.contributor.otherHo, Bao-
dc.contributor.otherLiu, Victor-
dc.contributor.otherRoberts, Matthew-
dc.contributor.otherThompson, James-
dc.contributor.otherSheehan-Dare, Gemma-
dc.contributor.otherAlghazo, Omar-
dc.contributor.otherAgrawal, Shikha-
dc.contributor.otherStricker, Phillip-
dc.contributor.otherHope, Thomas-
dc.contributor.otherHoffman, Michael-
dc.date2022-03-
dc.date.accessioned2022-03-28T02:15:26Z-
dc.date.available2022-03-28T02:15:26Z-
dc.date.issued2022-03-
dc.identifier.citationJ Nucl Med . 2022 Mar 17en_US
dc.identifier.issn0161-5505en_US
dc.identifier.issn2159-662Xen_US
dc.identifier.urihttp://hdl.handle.net/11434/2064-
dc.description.abstractBackground: Multi-parametric magnetic resonance imaging (mpMRI) is validated for the diagnosis of clinically significant prostate cancer (csPCa). 68Ga-PSMA -11 PET/CT (PSMA-PET/CT) combined with mpMRI has improved negative predictive value over mpMRI alone for csPCa. The aim of this post-hoc analysis of the PRIMARY study was to evaluate the clinical significance of patterns of intra-prostatic PSMA activity, proposing a 5- point PRIMARY score to optimise accuracy of PSMA-PET/CT for csPCa in a low prevalence population. Methods: The PRIMARY trial is a prospective multi-centre phase II imaging trial that enrolled biopsy-naïve men with suspected PCa, no prior biopsy, recent mpMRI (6 months) and planned for prostate biopsy. 291 men underwent mpMRI, PSMA-PET/CT and systematic +/- targeted biopsy. The mpMRI was read separately using PI-RADS (V2). PSMA-PET/CT (pelvic only) was acquired a minimum 60 minutes post injection. PSMA-PET/CT was centrally read for pattern (diffuse transition zone (TZ), symmetrical central zone (CZ), focal TZ or peripheral zone (PZ), and intensity (SUVmax). In this post-hoc analysis, a 5-level PRIMARY score was assigned based on analysis of the central read: 1. No pattern, 2. Diffuse TZ or CZ (no focal), 3. Focal TZ, 4. Focal PZ or 5. SUVmax ≥ 12. Two further readers independently assigned a PRIMARY score to 118 scans for inter-rater agreement. Associations between PRIMARY score and csPCa (ISUP≥2) were evaluated. Results: Of 291 men enrolled, 162 (56%) had csPCa. PRIMARY score-1 was present in 16% (47), score-2 in 19% (55), score-3 in 10% (29), score-4 in 40% (117) and score-5 in 15% (43). The proportion of patients with csPCa and PRIMARY score 1 to 5 was 8.5% (4/47), 27% (15/55), 38% (11/29), 76% (89/117) and 100% (43/43) respectively. Sensitivity, specificity, PPV and NPV for PRIMARY score 1,2 (low-risk patterns) vs PRIMARY score 3-5 (high-risk patterns) was 88%, 64%, 76% and 81%, compared to 83%, 53%, 69% and 72% for PI-RADS (2 vs 3-5) on mpMRI. The inter-rater agreements for PRIMARY score 1,2 vs. PRIMARY score 3-5 was 0.76 (CI: 0.64-0.88) and 0.64 (CI: 0.49-0.78). Conclusion: A PRIMARY score incorporating intra-prostatic pattern and intensity on PSMA-PET/CT shows potential with high diagnostic accuracy for csPCa. Further validation is warranted prior to implementation.en_US
dc.publisherSociety of Nuclear Medicine and Molecular Imaging (SNMMI)en_US
dc.subjectMRIen_US
dc.subjectMulti-Parametric MRIen_US
dc.subjectOncologyen_US
dc.subjectClinically Significant Prostate Canceren_US
dc.subjectcsPCaen_US
dc.subjectPET/CTen_US
dc.subjectPSMAen_US
dc.subjectProstate Specific Membrane Antigenen_US
dc.subjectIntra-Prostatic PSMA Activityen_US
dc.subjectDiagnostic Accuracyen_US
dc.subjectCancer Services Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.subjectUrology and Vascular Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.subjectEpworth Prostate Centre, Epworth HealthCare, Victoria, Australiaen_US
dc.titleThe PRIMARY Score: Using intra-prostatic PSMA PET/CT patterns to optimise prostate cancer diagnosis.en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.2967/jnumed.121.263448en_US
dc.identifier.journaltitleJournal of Nuclear Medicineen_US
dc.description.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35301240en_US
dc.description.affiliatesDepartment of Theranostics and Nuclear Medicine, St Vincent's Hospital Sydney, Australia.en_US
dc.description.affiliatesSchool of Public Health and Preventive Medicine, Monash University, Australia.en_US
dc.description.affiliatesMolecular Imaging and Therapeutic Nuclear Medicine, Peter MacCallum Cancer, Melbourne.en_US
dc.description.affiliatesDepartment of Urology, Royal Brisbane and Women's Hospital, Brisbane.en_US
dc.description.affiliatesDepartment of Urology, St. George Hospital, Australia.en_US
dc.description.affiliatesDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.en_US
dc.description.affiliatesGosford Hospital.en_US
dc.description.affiliatesGarvan Institute of Medical Research.en_US
dc.description.affiliatesPeter MacCallum Cancer Centre, Melbourne, Australia.en_US
dc.description.affiliatesSt. Vincent's Prostate Cancer Centre, Darlinghurst, NSW, Australia.en_US
dc.description.affiliatesUniversity of California, San Francisco.en_US
dc.type.studyortrialClinical Trialen_US
dc.type.contenttypeTexten_US
Appears in Collections:Cancer Services
Epworth Prostate Centre
UroRenal, Vascular

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