Evidence map›Paper›PMID 32773013›Full record

Trial reportHealth technology assessment (Winchester, England)2020

Active monitoring, radical prostatectomy and radical radiotherapy in PSA-detected clinically localised prostate cancer: the ProtecT three-arm RCT.

Freddie C Hamdy, Jenny L Donovan, J Athene Lane, Malcolm Mason, Chris Metcalfe, Peter Holding, Julia Wade, Sian Noble, Kirsty Garfield, Grace Young and 26 more

Open access · diamondAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Health technology assessment (Winchester, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 5% 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.

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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

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  13. Listening to the Patient Voice Adds Value to Cancer Clinical Trials.Journal of the National Cancer Institute · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

36 authors at 15 institutions in 1 country.

Freddie C HamdyNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0003-2627-2154
Jenny L DonovanBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-6488-5472
J Athene LaneBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-7578-4925
Malcolm MasonSchool of Medicine, University of Cardiff, Cardiff, UK.ORCID 0000-0003-1505-2869
Chris MetcalfeBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0001-8318-8907
Peter HoldingNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0001-9175-4411
Julia WadeBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0001-6486-6477
Sian NobleBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-8011-0722
Kirsty GarfieldBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-8301-3602
Grace YoungBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-5210-1183
Michael DavisBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-3624-3456
Tim J PetersBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0003-2881-4180
Emma L TurnerBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0003-2575-387X
Richard M MartinBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-7992-7719
Jon OxleyDepartment of Cellular Pathology, North Bristol NHS Trust, Bristol, UK.ORCID 0000-0002-4348-0273
Mary RobinsonDepartment of Cellular Pathology, Royal Victoria Infirmary, Newcastle upon Tyne, UK.ORCID 0000-0003-3488-3828
John StaffurthDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.ORCID 0000-0002-7834-3172
Eleanor WalshBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0001-7696-3661
Jane BlazebyBristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0002-3354-3330
Richard BryantNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-8330-9251
Prasad BollinaDepartment of Urology and Surgery, Western General Hospital, University of Edinburgh, Edinburgh, UK.ORCID 0000-0001-5912-2772
James CattoAcademic Urology Unit, University of Sheffield, Sheffield, UK.ORCID 0000-0003-2787-8828
Andrew DobleDepartment of Urology, Addenbrooke's Hospital, Cambridge, UK.ORCID 0000-0002-9131-0623
Alan DohertyDepartment of Urology, Queen Elizabeth Hospital, Birmingham, UK.ORCID 0000-0003-3444-4710
David GillattDepartment of Urology, Southmead Hospital and Bristol Urological Institute, Bristol, UK.ORCID 0000-0003-4581-9346
Vincent GnanapragasamDepartment of Urology, Addenbrooke's Hospital, Cambridge, UK.ORCID 0000-0003-4722-4207
Owen HughesDepartment of Urology, Cardiff and Vale University Health Board, Cardiff, UK.ORCID 0000-0002-1513-3629
Roger KockelberghDepartment of Urology, University Hospitals of Leicester, Leicester, UK.ORCID 0000-0003-2261-3628
Howard KynastonDepartment of Urology, Cardiff and Vale University Health Board, Cardiff, UK.ORCID 0000-0003-1902-9930
Alan PaulDepartment of Urology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.ORCID 0000-0001-6467-1864
Edgar PaezDepartment of Urology, Freeman Hospital, Newcastle upon Tyne, UK.ORCID 0000-0002-1168-6736
Philip PowellDepartment of Urology, Freeman Hospital, Newcastle upon Tyne, UK.ORCID 0000-0001-5215-3613
Stephen PrescottDepartment of Urology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.ORCID 0000-0002-2737-7364
Derek RosarioAcademic Urology Unit, University of Sheffield, Sheffield, UK.ORCID 0000-0002-9086-3592
Edward RoweDepartment of Urology, Southmead Hospital and Bristol Urological Institute, Bristol, UK.ORCID 0000-0002-6423-3474
David NealNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-6033-5086
University of Bristol · GBUniversity of Oxford · GBAddenbrooke's Hospital · GBCardiff and Vale University Health Board · GBCardiff University · GBFreeman Hospital · GBLeeds Teaching Hospitals NHS Trust · GBSouthmead Hospital · GBUniversity of Sheffield · GBNorth Bristol NHS Trust · GBQueen Elizabeth Hospital Birmingham · GBRoyal Victoria Infirmary · GBUniversity Hospitals of Leicester NHS Trust · GBUniversity of Cambridge · GBWestern General Hospital · GB

Funding

Cancer Research UK 15064Cancer Research UK 22748Cancer Research UK 24432Department of Health 96/20/99Medical Research Council MR/K025643/1
6 · The paper itself

Abstract

backgroundProstate cancer is the most common cancer among men in the UK. Prostate-specific antigen testing followed by biopsy leads to overdetection, overtreatment as well as undertreatment of the disease. Evidence of treatment effectiveness has lacked because of the paucity of randomised controlled trials comparing conventional treatments.

objectivesTo evaluate the effectiveness of conventional treatments for localised prostate cancer (active monitoring, radical prostatectomy and radical radiotherapy) in men aged 50-69 years.

designA prospective, multicentre prostate-specific antigen testing programme followed by a randomised trial of treatment, with a comprehensive cohort follow-up.

settingProstate-specific antigen testing in primary care and treatment in nine urology departments in the UK.

participantsBetween 2001 and 2009, 228,966 men aged 50-69 years received an invitation to attend an appointment for information about the Prostate testing for cancer and Treatment (ProtecT) study and a prostate-specific antigen test; 82,429 men were tested, 2664 were diagnosed with localised prostate cancer, 1643 agreed to randomisation to active monitoring (

interventionsThe interventions were active monitoring, radical prostatectomy and radical radiotherapy. TRIAL PRIMARY OUTCOME MEASURE: Definite or probable disease-specific mortality at the 10-year median follow-up in randomised participants. SECONDARY OUTCOME MEASURES: Overall mortality, metastases, disease progression, treatment complications, resource utilisation and patient-reported outcomes.

resultsThere were no statistically significant differences between the groups for 17 prostate cancer-specific ( LIMITATIONS: A single prostate-specific antigen test and transrectal ultrasound biopsies were used. There were very few non-white men in the trial. The majority of men had low- and intermediate-risk disease. Longer follow-up is needed.

conclusionsAt a median follow-up point of 10 years, prostate cancer-specific mortality was low, irrespective of the assigned treatment. Radical prostatectomy and radical radiotherapy reduced disease progression and metastases, but with side effects. Further work is needed to follow up participants at a median of 15 years.

trial registrationCurrent Controlled Trials ISRCTN20141297.

fundingThis project was funded by the National Institute for Health Research Health Technology Assessment programme and will be published in full in

Indexed as

Disease-Free SurvivalPatient Reported Outcome MeasuresProstatectomyWatchful WaitingAgedHumansMaleMiddle AgedProspective StudiesProstate-Specific AntigenProstatic NeoplasmsQuality of LifeProstate-Specific AntigenACTIVE MONITORINGPROSTATE CANCERPROSTATE-SPECIFIC ANTIGEN TESTINGQUALITY OF LIFERADICAL PROSTATECTOMYRADICAL RADIOTHERAPYRADICAL TREATMENTRANDOMISED CLINICAL TRIAL

Identifiers

PMID32773013
PMCPMC7443739
OpenAlexW3048532187

What OpenQuestion holds

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Registered trials

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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.