Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34572
Title: Clinical Trial Protocol for PRIMARY2: A Multicentre, Phase 3, Randomised Controlled Trial Investigating the Additive Diagnostic Value of [68Ga]Ga-PSMA-11 Positron Emission Tomography/Computed Tomography in Men with Negative or Equivocal Multiparametric Magnetic Resonance Imaging for the Diagnosis of Clinically Significant Prostate Cancer.
Austin Authors: Buteau, James P;Moon, Daniel;Fahey, Michael T;Roberts, Matthew J;Thompson, James;Murphy, Declan G;Papa, Nathan;Mitchell, Catherine;De Abreu Lourenco, Richard;Dhillon, Haryana M;Kasivisvanathan, Veeru;Francis, Roslyn J;Stricker, Phillip;Agrawal, Shihka;O'Brien, Jonathan;McVey, Aoife ;Sharma, Gaurav;Levy, Sidney;Ayati, Narjess ;Nguyen, Andrew;Lee, Su-Faye;Pattison, David A;Sivaratnam, Dinesh;Frydenberg, Mark;Du, Yang;Titus, Jehan;Lee, Sze Ting ;Ischia, Joseph J ;Jack, Greg;Hofman, Michael S;Emmett, Louise
Affiliation: Prostate Cancer Theranostics and Imaging Centre of Excellence, Peter MacCallum Cancer Centre, Melbourne, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia.
Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Australia; Royal Melbourne Clinical School, University of Melbourne, Melbourne, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia; Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.
Department of Urology, Royal Brisbane and Women's Hospital, Brisbane, Australia; UQ Centre for Clinical Research, Faculty of Medicine, University of Queensland, Brisbane, Australia.
Department of Urology, St. George Hospital, Sydney, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia; Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Australia.
School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia; Department of Pathology, Peter MacCallum Cancer Centre, Melbourne, Australia.
Centre for Health Economics Research and Evaluation, University of Technology Sydney, Sydney, Australia.
Psycho-Oncology Cooperative Research Group, Centre for Medical Psychology & Evidence-based Decision-making, University of Sydney, Camperdown, Australia.
Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Australia; Division of Surgery and Interventional Science, University College London, London, UK.
Department of Nuclear Medicine, Sir Charles Gairdner Hospital, Perth, WA, Australia; Medical School, University of Western Australia, Perth, Australia.
St. Vincent's Prostate Cancer Research Centre, Garvan Institute, UNSW Sydney, Sydney, Australia; Department of Urology, St. Vincent's Hospital, Sydney, Australia.
Department of Theranostics and Nuclear Medicine, St. Vincent's Hospital, Sydney, Australia; Faculty of Medicine, UNSW Sydney, Sydney, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia; Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia; Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Australia.
Prostate Cancer Theranostics and Imaging Centre of Excellence, Peter MacCallum Cancer Centre, Melbourne, Australia.
Department of Theranostics and Nuclear Medicine, St. Vincent's Hospital, Sydney, Australia; Faculty of Medicine, UNSW Sydney, Sydney, Australia.
Department of Nuclear Medicine and Specialised PET Services, Royal Brisbane and Women's Hospital, Brisbane, Australia; School of Medicine, University of Queensland, Brisbane, Australia.
Department of Nuclear Medicine, Royal Melbourne Hospital, Melbourne, Australia; Department of Nuclear Medicine, Cabrini Health, Melbourne, Australia.
Department of Surgery, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Australia; Cabrini Research, Cabrini Health, Melbourne, Australia.
Department of Nuclear Medicine, PET and Bone Densitometry, South Australia Medical Imaging, Royal Adelaide Hospital, Adelaide, Australia.
Department of Urology, Royal Adelaide Hospital, Adelaide, Australia.
Department of Medicine, University of Melbourne, Melbourne, Australia; Department of Molecular Imaging and Therapy, Austin Health, Melbourne, Australia.
Surgery (University of Melbourne)
Department of Theranostics and Nuclear Medicine, St. Vincent's Hospital, Sydney, Australia; Faculty of Medicine, UNSW Sydney, Sydney, Australia.
Issue Date: 6-Dec-2023
Date: 2023
Publication information: European Urology Oncology 2023-12-06
Abstract: Multiparametric magnetic resonance imaging (mpMRI) has an established role for the diagnosis of clinically significant prostate cancer (sPCa). The PRIMARY trial demonstrated that [68Ga]Ga-PSMA-11 positron emission tomography/computed tomography (PET/CT) was associated with a significant improvement in sensitivity and negative predictive value for sPCa detection. To demonstrate that addition of prostate-specific membrane antigen (PSMA) radioligand PET/CT will enable some men to avoid transperineal prostate biopsy without missing sPCa, and will facilitate biopsy targeting of PSMA-avid sites. This multicentre, two-arm, phase 3, randomised controlled trial will recruit 660 participants scheduled to undergo biopsy. Eligible participants will have clinical suspicion of sPCa with a Prostate Imaging-Reporting and Data System (PI-RADS) score of 2 and red flags, or a PI-RADS score of 3 on mpMRI (PI-RADS v2). Participants will be randomised at a 1:1 ratio in permuted blocks stratified by centre. The trial is registered on ClinicalTrials.gov as NCT05154162. In the experimental arm, participants will undergo pelvic PSMA PET/CT. Local and central reviewers will interpret scans independently using the PRIMARY score. Participants with a positive result will undergo targeted transperineal prostate biopsies, whereas those with a negative result will undergo prostate-specific antigen monitoring alone. In the control arm, all participants undergo template transperineal prostate biopsies. Participants will be followed for subsequent clinical care for up to 2 yr after randomisation. sPCa is defined as Gleason score 3 + 4 (≥10%) = 7 disease (grade group 2) or higher on transperineal prostate biopsy. Avoidance of transperineal prostate biopsy will be measured at 6 mo from randomisation. The primary endpoints will be analysed on an intention-to-treat basis. Patient enrolment began in March 2022, with recruitment expected to take 36 mo. For patients with suspected prostate cancer who have nonsuspicious or unclear MRI (magnetic resonance imaging) scan findings, a different type of scan (called PSMA PET/CT; prostate-specific membrane antigen positron emission tomography/computed tomography) may identify men who could avoid an invasive prostate biopsy. This type of scan could also help urologists in better targeting of samples from suspicious lesions during prostate biopsies.
URI: https://ahro.austin.org.au/austinjspui/handle/1/34572
DOI: 10.1016/j.euo.2023.11.008
ORCID: 
Journal: European Urology Oncology
PubMed URL: 38061976
ISSN: 2588-9311
Type: Journal Article
Subjects: Clinically significant prostate cancer
Diagnosis
Multiparametric magnetic resonance imaging
Positron emission tomography scan
Prostate cancer
Prostate-specific membrane antigen
Appears in Collections:Journal articles

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