Evidence map›Paper›PMID 32209449›Full record

Trial reportLancet (London, England)2020

Prostate-specific membrane antigen PET-CT in patients with high-risk prostate cancer before curative-intent surgery or radiotherapy (proPSMA): a prospective, randomised, multicentre study.

Michael S Hofman, Nathan Lawrentschuk, Roslyn J Francis, Colin Tang, Ian Vela, Paul Thomas, Natalie Rutherford, Jarad M Martin, Mark Frydenberg, Ramdave Shakher and 17 more

2 registry-linked trialsAbstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Lancet (London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 995 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
995citing papers in PubMed, 7 pooled it
140.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05123300 naterminatednot on this mapstarted 2021, after this paper: background citation

PRISMA-PET - Primary Staging of Prostate Cancer: A Randomized Controlled Trial Comparing 18F-PSMA-1007 PET/CT to Conventional Imaging

TypeinterventionalSponsorOdense University HospitalRan2021 to 2025Enrolled385ConditionsProstate CancerArms18F-PSMA-1007
NCT07426094 phase2 / phase3recruitingnot on this mapstarted 2026, after this paper: background citation

PRO-BOOST-N: A Randomized Phase II/III Trial Evaluating Prostate-First Versus Combined Prostate and Nodal Dose Escalation in PSMA PET-Staged Node-Positive Prostate Cancer Using an Ultrahypofractionated Whole-Pelvis Radiotherapy Platform

TypeinterventionalSponsorAffidea Nu-med Center of Oncological DIagnostics and TherapyRan2026 to 2035Enrolled600ConditionsProstate Cancer, Brachytherapy, Stereotactic Body Radiation Therapy (SBRT), Dose Escalation: Solid TumorsArmsUltrahypofractionated Whole-Pelvis Radiotherapy, SBRT-Based Prostate Radiotherapy (No Boost), Ablative Prostate Boost, Intermediate Nodal Dose Escalation, Higher Nodal Dose Escalation
3 · Its place in the literature

Who cites it

995 citing papers in PubMed, 7 syntheses or guidelines pooled it, 1,871 citations in OpenAlex.

  1. Pooled it
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  5. Is there a role of PSMA-PET in focal therapy planning and follow-up?Prostate cancer and prostatic diseases · 2026
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  8. Comparison of [European journal of nuclear medicine and molecular imaging · 2026
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  10. A prospective head-to-head comparison ofEuropean journal of nuclear medicine and molecular imaging · 2026
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  12. [European journal of nuclear medicine and molecular imaging · 2026
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  13. An intra-patient contemporaneous comparison ofEuropean journal of nuclear medicine and molecular imaging · 2026
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  15. LASER: A Phase 2 Trial ofJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
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  16. The German Cancer Consortium (DKTK) multi-center prospective phase 1/2European journal of nuclear medicine and molecular imaging · 2026
    Trial
  17. Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
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  18. Review
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935 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 17 institutions in 1 country.

Michael S HofmanMolecular Imaging and Therapeutic Nuclear Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia. Electronic address: michael.hofman@petermac.org.
Nathan LawrentschukSir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia; Department of Surgery, Austin Health, Melbourne, VIC, Australia; Urological Society of Australia and New Zealand, NSW, Australia.
Roslyn J FrancisDepartment of Nuclear Medicine, Sir Charles Gairdner Hospital, Perth, WA, Australia; University of Western Australia, Faculty of Health and Medical Sciences, Perth, WA, Australia; ARTnet, NSW, Australia.
Colin TangDepartment of Radiation Oncology, Sir Charles Gairdner Hospital, Perth, Australia.
Ian VelaDepartment of Urology, Princess Alexandra Hospital, Australian Prostate Cancer Research Centre-Queensland, Queensland University of Technology, Translational Research Institute, Brisbane, QLD, Australia.
Paul ThomasDepartment of Nuclear Medicine, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia; Faculty of Medicine, University of Queensland, Brisbane, QLD, Australia.
Natalie RutherfordDepartment of Nuclear Medicine, Hunter New England Health, Newcastle, NSW, Australia.
Jarad M MartinSchool of Medicine and Public Health, University of Newcastle, Newcastle, NSW, Australia.
Mark FrydenbergDepartment of Surgery, Monash University and Cabrini Institute, Cabrini Health, Melbourne, VIC, Australia.
Ramdave ShakherMonash Health Imaging, Monash Health, Melbourne, VIC, Australia.
Lih-Ming WongDepartment of Urology and Surgery, St Vincent's Health Melbourne, University of Melbourne, Melbourne, VIC, Australia.
Kim TaubmanDepartment of Medical Imaging, PET/CT and St Vincent's Private Radiology, St Vincent's Health, Melbourne, VIC, Australia.
Sze Ting LeeDepartment of Molecular Imaging and Therapy, Austin Health, Melbourne, VIC, Australia.
Edward HsiaoUniversity of Sydney, Department of Nuclear Medicine and PET, Royal North Shore Hospital, Sydney, NSW, Australia.
Paul RoachUniversity of Sydney, Department of Nuclear Medicine and PET, Royal North Shore Hospital, Sydney, NSW, Australia.
Michelle NottageClinical and Research Imaging Centre, South Australian Health and Medical Research Institute, Adelaide, SA, Australia; Dr Jones and Partners Medical Imaging, Adelaide, SA, Australia.
Ian KirkwoodDepartment of Nuclear Medicine and PET, Royal Adelaide Hospital, Adelaide, SA, Australia; Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, SA, Australia.
Dickon HayneUWA Medical School, University of Western Australia, Perth, WA, Australia.
Emma LinkCentre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.
Petra MarusicMolecular Imaging and Therapeutic Nuclear Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Anetta MateraCentre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Alan HerschtalCentre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Amir IravaniMolecular Imaging and Therapeutic Nuclear Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.
Rodney J HicksMolecular Imaging and Therapeutic Nuclear Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.
Scott WilliamsDivision of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia; Australian and New Zealand Urogenital and Prostate Cancer Trials Group, NSW, Australia.
Declan G MurphyDivision of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia.
proPSMA Study Group Collaborators
Peter MacCallum Cancer Centre · AUThe University of Melbourne · AUAustin Health · AUThe University of Western Australia · AUAustralian and New Zealand Urogenital and Prostate Cancer Trials Group · AUCabrini Hospital · AUHunter New England Local Health District · AUMonash Health · AUPrincess Alexandra Hospital · AURoyal Adelaide Hospital · AURoyal North Shore Hospital · AUSir Charles Gairdner Hospital · AUSouth Australian Health and Medical Research Institute · AUSt Vincent's Health · AUThe University of Queensland · AUThe University of Sydney · AUUniversity of Newcastle Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConventional imaging using CT and bone scan has insufficient sensitivity when staging men with high-risk localised prostate cancer. We aimed to investigate whether novel imaging using prostate-specific membrane antigen (PSMA) PET-CT might improve accuracy and affect management.

methodsIn this multicentre, two-arm, randomised study, we recruited men with biopsy-proven prostate cancer and high-risk features at ten hospitals in Australia. Patients were randomly assigned to conventional imaging with CT and bone scanning or gallium-68 PSMA-11 PET-CT. First-line imaging was done within 21 days following randomisation. Patients crossed over unless three or more distant metastases were identified. The primary outcome was accuracy of first-line imaging for identifying either pelvic nodal or distant-metastatic disease defined by the receiver-operating curve using a predefined reference-standard including histopathology, imaging, and biochemistry at 6-month follow-up. This trial is registered with the Australian New Zealand Clinical Trials Registry, ANZCTR12617000005358.

findingsFrom March 22, 2017 to Nov 02, 2018, 339 men were assessed for eligibility and 302 men were randomly assigned. 152 (50%) men were randomly assigned to conventional imaging and 150 (50%) to PSMA PET-CT. Of 295 (98%) men with follow-up, 87 (30%) had pelvic nodal or distant metastatic disease. PSMA PET-CT had a 27% (95% CI 23-31) greater accuracy than that of conventional imaging (92% [88-95] vs 65% [60-69]; p<0·0001). We found a lower sensitivity (38% [24-52] vs 85% [74-96]) and specificity (91% [85-97] vs 98% [95-100]) for conventional imaging compared with PSMA PET-CT. Subgroup analyses also showed the superiority of PSMA PET-CT (area under the curve of the receiver operating characteristic curve 91% vs 59% [32% absolute difference; 28-35] for patients with pelvic nodal metastases, and 95% vs 74% [22% absolute difference; 18-26] for patients with distant metastases). First-line conventional imaging conferred management change less frequently (23 [15%] men [10-22] vs 41 [28%] men [21-36]; p=0·008) and had more equivocal findings (23% [17-31] vs 7% [4-13]) than PSMA PET-CT did. Radiation exposure was 10·9 mSv (95% CI 9·8-12·0) higher for conventional imaging than for PSMA PET-CT (19·2 mSv vs 8·4 mSv; p<0·001). We found high reporter agreement for PSMA PET-CT (κ=0·87 for nodal and κ=0·88 for distant metastases). In patients who underwent second-line image, management change occurred in seven (5%) of 136 patients following conventional imaging, and in 39 (27%) of 146 following PSMA PET-CT.

interpretationPSMA PET-CT is a suitable replacement for conventional imaging, providing superior accuracy, to the combined findings of CT and bone scanning.

fundingMovember and Prostate Cancer Foundation of Australia. VIDEO ABSTRACT.

Indexed as

AgedAntigens, SurfaceBiomarkersGlutamate Carboxypeptidase IIHumansLymphatic MetastasisMaleMiddle AgedNeoplasm MetastasisPositron Emission Tomography Computed TomographyProspective StudiesProstatic NeoplasmsSensitivity and SpecificityWhole Body ImagingAntigens, SurfaceBiomarkersFOLH1 protein, humanGlutamate Carboxypeptidase II

Identifiers

PMID32209449
OpenAlexW3012827461

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.