Evidence map›Paper›PMID 42080884›Full record

ArticleEuropean radiology2026

Multicentre validation of the PRECISE scoring system for prostate MRI during active surveillance.

Francesco Giganti, Riccardo Leni, Vinayak Wagaskar, Giorgio Gandaglia, Tristan Barrett, Valeria Panebianco, Francesco Sanguedolce, Erik Jrj van der Hoeven, Sangeet Ghai, Jeremy Grummet and 22 more

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in European radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors.

Francesco GigantiDivision of Surgery and Interventional Science, University College London, London, UK. f.giganti@ucl.ac.uk.ORCID http://orcid.org/0000-0001-5218-6431
Riccardo LeniDivision of Oncology/Unit of Urology, Soldera Prostate Cancer Lab, URI, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Vinayak WagaskarDepartment of Urology, Icahn School of Medicine at Mount Sinai Hospital, New York, NY, USA.
Giorgio GandagliaDivision of Oncology/Unit of Urology, Soldera Prostate Cancer Lab, URI, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Tristan BarrettDepartment of Radiology, Addenbrooke's Hospital and University of Cambridge, Cambridge, UK.
Valeria PanebiancoDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University/Policlinico Umberto I, Rome, Italy.
Francesco SanguedolceDepartment of Urology, Fundació Puigvert, Barcelona, Spain.
Erik Jrj van der HoevenDepartment of Radiology, St Antonius Hospital, Utrecht, The Netherlands.
Sangeet GhaiJoint Department of Medical Imaging, University Health Network-Mt Sinai Hospital-Women's College Hospital, University of Toronto, Toronto, ON, Canada.
Jeremy GrummetDepartment of Surgery, Alfred Health, School of Translational Medicine, Monash University, Melbourne, Australia.
Jasmin GmeinerDepartment of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Jan Philipp RadtkeDepartment of Urology, Medical Faculty, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
Ryan D WardAbdominal Imaging Section, Diagnostics Institute, Cleveland Clinic, Cleveland, OH, USA.
Ronaldo Hueb BaroniImaging Section, Hospital Israelita Albert Einstein, Sao Paulo, Brazil.
Francesco PorpigliaDivision of Urology, Department of Oncology, San Luigi Gonzaga Hospital, University of Turin, Turin, Italy.
Juan Gomez RivasDepartment of Urology, Health Research Institute, Hospital Clinico San Carlos, Madrid, Spain.
Fabio ZattoniDepartment of Surgery, Oncology, and Gastroenterology, Urology Clinic, University of Padua, Padua, Italy.
Raphaële Renard-PennaDepartment of Imaging, Hôpital Pitié Salpêtrière APHP-Sorbonne University, Paris, France.
Claudia KeschDepartment of Urology, University of Duisburg-Essen and German Cancer Consortium (DKTK), University Hospital Essen, Essen, Germany.
Marco GattiDivision of Radiology, Department of Surgical Sciences, Molinette Hospital, Città della Salute e della Scienza and University of Turin, Turin, Italy.
Nicola SchiedaDepartment of Radiology, The University of Ottawa, Ottawa, ON, Canada.
Guillaume PloussardLa Croix du Sud Hospital, Department of Urology, Quint-Fonsegrives, France.
Sara LewisDepartment of Radiology, Icahn School of Medicine at Mount Sinai Hospital, New York, NY, USA.
Giorgio BrembillaDepartment of Radiology, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.
Christof KastnerDepartment of Urology, Addenbrooke's Hospital and University of Cambridge, Cambridge, UK.
Emanuele MessinaDepartment of Radiological Sciences, Oncology and Pathology, Sapienza University/Policlinico Umberto I, Rome, Italy.
Ash TewariDepartment of Urology, Icahn School of Medicine at Mount Sinai Hospital, New York, NY, USA.
Caroline M MooreDivision of Surgery and Interventional Science, University College London, London, UK.
Massimo Valerio *Department of Urology, Lausanne University Hospital, Lausanne, Switzerland.
Armando Stabile *Division of Oncology/Unit of Urology, Soldera Prostate Cancer Lab, URI, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Veeru Kasivisvanathan *Division of Surgery and Interventional Science, University College London, London, UK.
Young Academic Urologists Active Surveillance Initiative

Funding

CRIS Cancer Foundation 20YOUN15Prostate Cancer Foundation 20YOUN15
6 · The paper itself

Abstract

objectivesThe Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) recommendations assess radiological change in serial MRI during active surveillance (AS) for prostate cancer. PRECISE 1-2 indicates radiological regression, PRECISE 3 stability, and PRECISE 4-5 progression. Our aim was to test the PRECISE score as a predictive tool for disease progression in a multicentre international setting. MATERIALS AND

methodsThis is a retrospective study in which we collected data from 22 international centres from December 2005 to July 2022, applying two entry criteria: (1) at least two scans (baseline and follow-up); (2) at least two biopsies (baseline and follow-up, the latter after the second scan). Local radiologists reported scans according to PRECISE. Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) according to different biopsy thresholds and definitions of progression were calculated.

resultsA total of 1667 patients were included. Median follow-up was 4 years (IQR: 2.1-6.3). A total of 1248 (75%) patients underwent two MRIs and immediate subsequent biopsy, 300 (24%) of which had biopsy progression to Grade Group ≥ 2 and 77 (6%) to Grade Group ≥ 3. Patients with PRECISE 4-5 had 4.53-fold increased odds (95% CI: 3.37-6.12; p < 0.001) of biopsy progression compared to PRECISE 1-3. Using a PRECISE ≥ 4 cutoff to perform follow-up biopsies, overall sensitivity, specificity, PPV and NPV were 57%, 79%, 46%, and 85% for the first follow-up scan.

conclusionThe PRECISE recommendations could lead to timely identification of patients on AS who progress on MRI, prompting re-biopsy or treatment, and safe reduction of repeat biopsies for those with stable MRI and prostate-specific antigen kinetics. KEY POINTS: Question Can the PRECISE scoring system for monitoring prostate cancer lesions on active surveillance on MRI predict disease progression and avoid unnecessary biopsies? Findings The PRECISE score effectively predicts prostate cancer progression, with PRECISE 4-5 (progression) scores indicating 4.53-fold increased odds of biopsy progression compared to PRECISE 1-3 (regression/stability). Clinical relevance This study validates PRECISE as a tool for managing patients on active surveillance. It can help clinicians identify those needing timely re-biopsy or treatment, while reducing unnecessary biopsies in patients with stable disease on imaging and PSA kinetics.

Indexed as

Magnetic Resonance ImagingProstatic NeoplasmsWatchful WaitingAgedBiopsyClinical RelevanceDisease ProgressionHumansMaleMiddle AgedProstateReproducibility of ResultsRetrospective StudiesSensitivity and SpecificityMagnetic resonance imagingProstate biopsyProstatic neoplasms

Identifiers

PMID42080884
PMCPMC13574842

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