EAU-EANM-ESTRO-ESUR-SIOG Prostate Cancer Guideline Panel Consensus Statements for Deferred Treatment with Curative Intent for Localised Prostate Cancer from an International Collaborative Study (DETECTIVE Study).

Active surveillance and monitoring Clinical practice guidelines Consensus group meeting Consensus statements Deferred treatment with curative intent Delphi survey Eligibility Follow-up Localised prostate cancer Outcome measures Reclassification

Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 05 07 2019
accepted: 11 09 2019
pubmed: 8 10 2019
medline: 18 12 2020
entrez: 8 10 2019
Statut: ppublish

Résumé

There is uncertainty in deferred active treatment (DAT) programmes, regarding patient selection, follow-up and monitoring, reclassification, and which outcome measures should be prioritised. To develop consensus statements for all domains of DAT. A protocol-driven, three phase study was undertaken by the European Association of Urology (EAU)-European Association of Nuclear Medicine (EANM)-European Society for Radiotherapy and Oncology (ESTRO)-European Association of Urology Section of Urological Research (ESUR)-International Society of Geriatric Oncology (SIOG) Prostate Cancer Guideline Panel in conjunction with partner organisations, including the following: (1) a systematic review to describe heterogeneity across all domains; (2) a two-round Delphi survey involving a large, international panel of stakeholders, including healthcare practitioners (HCPs) and patients; and (3) a consensus group meeting attended by stakeholder group representatives. Robust methods regarding what constituted the consensus were strictly followed. A total of 109 HCPs and 16 patients completed both survey rounds. Of 129 statements in the survey, consensus was achieved in 66 (51%); the rest of the statements were discussed and voted on in the consensus meeting by 32 HCPs and three patients, where consensus was achieved in additional 27 statements (43%). Overall, 93 statements (72%) achieved consensus in the project. Some uncertainties remained regarding clinically important thresholds for disease extent on biopsy in low-risk disease, and the role of multiparametric magnetic resonance imaging in determining disease stage and aggressiveness as a criterion for inclusion and exclusion. Consensus statements and the findings are expected to guide and inform routine clinical practice and research, until higher levels of evidence emerge through prospective comparative studies and clinical trials. We undertook a project aimed at standardising the elements of practice in active surveillance programmes for early localised prostate cancer because currently there is great variation and uncertainty regarding how best to conduct them. The project involved large numbers of healthcare practitioners and patients using a survey and face-to-face meeting, in order to achieve agreement (ie, consensus) regarding best practice, which will provide guidance to clinicians and researchers.

Sections du résumé

BACKGROUND BACKGROUND
There is uncertainty in deferred active treatment (DAT) programmes, regarding patient selection, follow-up and monitoring, reclassification, and which outcome measures should be prioritised.
OBJECTIVE OBJECTIVE
To develop consensus statements for all domains of DAT.
DESIGN, SETTING, AND PARTICIPANTS METHODS
A protocol-driven, three phase study was undertaken by the European Association of Urology (EAU)-European Association of Nuclear Medicine (EANM)-European Society for Radiotherapy and Oncology (ESTRO)-European Association of Urology Section of Urological Research (ESUR)-International Society of Geriatric Oncology (SIOG) Prostate Cancer Guideline Panel in conjunction with partner organisations, including the following: (1) a systematic review to describe heterogeneity across all domains; (2) a two-round Delphi survey involving a large, international panel of stakeholders, including healthcare practitioners (HCPs) and patients; and (3) a consensus group meeting attended by stakeholder group representatives. Robust methods regarding what constituted the consensus were strictly followed.
RESULTS AND LIMITATIONS CONCLUSIONS
A total of 109 HCPs and 16 patients completed both survey rounds. Of 129 statements in the survey, consensus was achieved in 66 (51%); the rest of the statements were discussed and voted on in the consensus meeting by 32 HCPs and three patients, where consensus was achieved in additional 27 statements (43%). Overall, 93 statements (72%) achieved consensus in the project. Some uncertainties remained regarding clinically important thresholds for disease extent on biopsy in low-risk disease, and the role of multiparametric magnetic resonance imaging in determining disease stage and aggressiveness as a criterion for inclusion and exclusion.
CONCLUSIONS CONCLUSIONS
Consensus statements and the findings are expected to guide and inform routine clinical practice and research, until higher levels of evidence emerge through prospective comparative studies and clinical trials.
PATIENT SUMMARY RESULTS
We undertook a project aimed at standardising the elements of practice in active surveillance programmes for early localised prostate cancer because currently there is great variation and uncertainty regarding how best to conduct them. The project involved large numbers of healthcare practitioners and patients using a survey and face-to-face meeting, in order to achieve agreement (ie, consensus) regarding best practice, which will provide guidance to clinicians and researchers.

Identifiants

pubmed: 31587989
pii: S0302-2838(19)30740-7
doi: 10.1016/j.eururo.2019.09.020
pii:
doi:

Types de publication

Consensus Development Conference Journal Article Practice Guideline Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

790-813

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Thomas B L Lam (TBL)

Academic Urology Unit, University of Aberdeen, Aberdeen, UK; Department of Urology, Aberdeen Royal Infirmary, Aberdeen, UK. Electronic address: thomas.lam@nhs.net.

Steven MacLennan (S)

Academic Urology Unit, University of Aberdeen, Aberdeen, UK.

Peter-Paul M Willemse (PM)

Department of Urology, University Medical Center Utrecht, Utrecht, The Netherlands.

Malcolm D Mason (MD)

Division of Cancer and Genetics, School of Medicine Cardiff University, Velindre Cancer Centre, Cardiff, UK.

Karin Plass (K)

EAU Guidelines Office, Arnhem, The Netherlands.

Robert Shepherd (R)

EAU Guidelines Office, Arnhem, The Netherlands.

Chris H Bangma (CH)

Department of Urology, Erasmus University Medical Centre, Rotterdam, The Netherlands.

Anders Bjartell (A)

Department of Urology, Skåne University Hospital Malmö, Lund University, Lund, Sweden.

Alberto Bossi (A)

Department of Radiation Oncology, Gustave Roussy Institute, Villejuif, France.

Erik Briers (E)

Hasselt, Belgium.

Alberto Briganti (A)

Department of Urology, Scientific Institute and University Vita-Salute San Raffaele Hospital, Milan, Italy.

Karel T Buddingh (KT)

HagaZiekenhuis, The Hague, The Netherlands.

James W F Catto (JWF)

Academic Urology Unit, University of Sheffield, Sheffield, UK; Department of Urology, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

Maurizio Colecchia (M)

Uropathology Unit, Department of Pathology, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.

Brett W Cox (BW)

Department of Radiation Medicine, Zucker School of Medicine, Hempstead, New York, NY, USA.

Marcus G Cumberbatch (MG)

Academic Urology Unit, University of Sheffield, Sheffield, UK.

Niall F Davis (NF)

Department of Urology, Beaumont and Connolly Hospitals, Dublin, Ireland; Royal College of Surgeons in Ireland, Dublin, Ireland.

Maria De Santis (M)

Department of Urology, Charité University Hospital, Berlin, Germany.

Paolo Dell'Oglio (P)

Unit of Urology, Division of Oncology, Urological Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy; ORSI Academy, Melle, Belgium.

André Deschamps (A)

Europa Uomo, Antwerp, Belgium.

James F Donaldson (JF)

Academic Urology Unit, University of Aberdeen, Aberdeen, UK; Department of Urology, Aberdeen Royal Infirmary, Aberdeen, UK.

Shin Egawa (S)

Asian School of Urology, UAA, Jikei University School of Medicine, Tokyo, Japan.

Christian D Fankhauser (CD)

Department of Urology, University of Zurich, Zurich, Switzerland.

Stefano Fanti (S)

Department of Nuclear Medicine, Policlinico S. Orsola, University of Bologna, Italy.

Nicola Fossati (N)

Department of Urology, Scientific Institute and University Vita-Salute San Raffaele Hospital, Milan, Italy.

Giorgio Gandaglia (G)

Unit of Urology, Division of Oncology, Urological Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy.

Silke Gillessen (S)

Division of Cancer Sciences, University of Manchester and The Christie, Manchester, UK; Department of Medical Oncology and Haematology, Cantonal Hospital St. Gallen, University of Bern, Bern, Switzerland.

Nikolaos Grivas (N)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Tobias Gross (T)

Department of Urology, University of Bern, Bern, Switzerland.

Jeremy P Grummet (JP)

Department of Surgery, Central Clinical School, Monash University, Melbourne, Australia.

Ann M Henry (AM)

Leeds Cancer Centre, St. James's University Hospital, Leeds, UK.

Alexandre Ingels (A)

Department of Urology, Henri Mondor Hospital, Créteil, France.

Jacques Irani (J)

University Hospital of Bicêtre-Paris Sud-Saclay University, Le Kremlin Bicêtre, France.

Michael Lardas (M)

Department of Reconstructive Urology and Surgical Andrology, Metropolitan General, Athens, Greece.

Matthew Liew (M)

Department of Urology, Wrightington, Wigan and Leigh NHS Foundation Trust, Wigan, UK.

Daniel W Lin (DW)

Cancer Prevention Program, Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Urology, University of Washington, Seattle, WA, USA.

Lisa Moris (L)

Department of Urology, University Hospitals Leuven, Leuven, Belgium; Laboratory of Molecular Endocrinology, KU Leuven, Leuven, Belgium.

Muhammad Imran Omar (MI)

Academic Urology Unit, University of Aberdeen, Aberdeen, UK.

Karl H Pang (KH)

Academic Urology Unit, University of Sheffield, Sheffield, UK.

Catherine C Paterson (CC)

Academic Urology Unit, University of Aberdeen, Aberdeen, UK; University of Canberra, School of Nursing, Midwifery and Public Health, Canberra, Australia; Robert Gordon University, School of Nursing and Midwifery, Aberdeen, UK.

Raphaële Renard-Penna (R)

Academic Department of Radiology, Sorbonne Université, GRC no 5, ONCOTYPE-URO, AP-HP, Hôpital Pitié-Salpêtrière-Hôpital Tenon, Paris, France.

Maria J Ribal (MJ)

Uro-Oncology Unit, Hospital Clinic, University of Barcelona, Barcelona, Spain.

Monique J Roobol (MJ)

Department of Urology, Erasmus University Medical Centre, Rotterdam, The Netherlands.

Morgan Rouprêt (M)

Urology Department, Sorbonne Université, GRC no 5, ONCOTYPE-URO, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.

Olivier Rouvière (O)

Hospices Civils de Lyon, Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Lyon, France; Université de Lyon, Université Lyon 1, Faculté de Médecine Lyon Est, Lyon, France.

Gemma Sancho Pardo (G)

Department of Radiation Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Jonathan Richenberg (J)

Royal Sussex County Hospital Brighton and Brighton and Sussex Medical School, Brighton, Sussex, UK.

Ivo G Schoots (IG)

Department of Radiology and Nuclear Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands.

J P Michiel Sedelaar (JPM)

Department of Urology, Radboud University Medical Centre, Nijmegen, The Netherlands.

Phillip Stricker (P)

Department of Urology, St Vincents Hospital and Campus, Sydney, Australia; Garvan Institute of Research, Sydney, Australia.

Derya Tilki (D)

Martini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany; Department of Urology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

Susanne Vahr Lauridsen (S)

Department of Urology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Roderick C N van den Bergh (RCN)

Department of Urology, St. Antonius Hospital, Utrecht, The Netherlands.

Thomas Van den Broeck (T)

Department of Urology, University Hospitals Leuven, Leuven, Belgium.

Theodorus H van der Kwast (TH)

Department of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Henk G van der Poel (HG)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Geert J L H van Leenders (GJLH)

Department of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Murali Varma (M)

Department of Cellular Pathology, University Hospital of Wales, Cardiff, UK.

Philippe D Violette (PD)

Departments of Health Research Methods, Evidence and Impact (HEI) and Surgery, McMaster University, Hamilton, ON, Canada.

Christopher J D Wallis (CJD)

Division of Urology, Department of Surgery, University of Toronto, Toronto, ON, Canada; Department of Urology, Vanderbilt University Medical Center, Nashville, TN, USA.

Thomas Wiegel (T)

Department of Radiation Oncology, University Hospital Ulm, Ulm, Germany.

Karen Wilkinson (K)

University College London Hospitals, London, UK.

Fabio Zattoni (F)

Urology Unit, Academic Medical Centre Hospital, Udine, Italy.

James M O N'Dow (JMO)

Academic Urology Unit, University of Aberdeen, Aberdeen, UK; Department of Urology, Aberdeen Royal Infirmary, Aberdeen, UK.

Hendrik Van Poppel (H)

Department of Urology, University Hospitals Leuven, Leuven, Belgium.

Philip Cornford (P)

Royal Liverpool and Broadgreen Hospitals NHS Trust, Liverpool, UK.

Nicolas Mottet (N)

Department of Urology, University Hospital Jean Monnet, St. Etienne, France.

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Classifications MeSH