A modified Delphi study to develop a practical guide for selecting patients with prostate cancer for active surveillance.


Journal

BMC urology
ISSN: 1471-2490
Titre abrégé: BMC Urol
Pays: England
ID NLM: 100968571

Informations de publication

Date de publication:
04 Feb 2021
Historique:
received: 27 11 2020
accepted: 20 01 2021
entrez: 5 2 2021
pubmed: 6 2 2021
medline: 23 7 2021
Statut: epublish

Résumé

Active surveillance (AS) is a management option for men diagnosed with lower risk prostate cancer. There is wide variation in all aspects of AS internationally, from patient selection to investigations and follow-up intervals, and a lack of clear evidence on the optimal approach to AS. This study aimed to provide guidance for clinicians from an international panel of prostate cancer experts. A modified Delphi approach was undertaken, utilising two rounds of online questionnaires followed by a face-to-face workshop. Participants indicated their level of agreement with statements relating to patient selection for AS via online questionnaires on a 7-point Likert scale. Factors not achieving agreement were iteratively developed between the two rounds of questionnaires. Draft statements were presented at the face-to-face workshop for discussion and consensus building. 12 prostate cancer experts (9 urologists, 2 academics, 1 radiation oncologist) participated in this study from a range of geographical regions (4 USA, 4 Europe, 4 Australia). Complete agreement on statements presented to the participants was 29.4% after Round One and 69.0% after Round Two. Following robust discussions at the face-to-face workshop, agreement was reached on the remaining statements. PSA, PSA density, Multiparametric MRI, and systematic biopsy (with or without targeted biopsy) were identified as minimum diagnostic tests required upon which to select patients to recommend AS as a treatment option for prostate cancer. Patient factors and clinical parameters that identified patients appropriate to potentially receive AS were agreed. Genetic and genomic testing was not recommended for use in clinical decision-making regarding AS. The lack of consistency in the practice of AS for men with lower risk prostate cancer between and within countries was reflected in this modified Delphi study. There are, however, areas of common practice and agreement from which clinicians practicing in the current environment can use to inform their clinical practice to achieve the best outcomes for patients.

Sections du résumé

BACKGROUND BACKGROUND
Active surveillance (AS) is a management option for men diagnosed with lower risk prostate cancer. There is wide variation in all aspects of AS internationally, from patient selection to investigations and follow-up intervals, and a lack of clear evidence on the optimal approach to AS. This study aimed to provide guidance for clinicians from an international panel of prostate cancer experts.
METHODS METHODS
A modified Delphi approach was undertaken, utilising two rounds of online questionnaires followed by a face-to-face workshop. Participants indicated their level of agreement with statements relating to patient selection for AS via online questionnaires on a 7-point Likert scale. Factors not achieving agreement were iteratively developed between the two rounds of questionnaires. Draft statements were presented at the face-to-face workshop for discussion and consensus building.
RESULTS RESULTS
12 prostate cancer experts (9 urologists, 2 academics, 1 radiation oncologist) participated in this study from a range of geographical regions (4 USA, 4 Europe, 4 Australia). Complete agreement on statements presented to the participants was 29.4% after Round One and 69.0% after Round Two. Following robust discussions at the face-to-face workshop, agreement was reached on the remaining statements. PSA, PSA density, Multiparametric MRI, and systematic biopsy (with or without targeted biopsy) were identified as minimum diagnostic tests required upon which to select patients to recommend AS as a treatment option for prostate cancer. Patient factors and clinical parameters that identified patients appropriate to potentially receive AS were agreed. Genetic and genomic testing was not recommended for use in clinical decision-making regarding AS.
CONCLUSIONS CONCLUSIONS
The lack of consistency in the practice of AS for men with lower risk prostate cancer between and within countries was reflected in this modified Delphi study. There are, however, areas of common practice and agreement from which clinicians practicing in the current environment can use to inform their clinical practice to achieve the best outcomes for patients.

Identifiants

pubmed: 33541309
doi: 10.1186/s12894-021-00789-5
pii: 10.1186/s12894-021-00789-5
pmc: PMC7863517
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

18

Références

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Auteurs

Samuel W D Merriel (SWD)

College of Medicine and Health, University of Exeter, 1.18 College House, St Luke's Campus, Heavitree Road, Exeter, EX1 2LU, UK. s.w.d.merriel@exeter.ac.uk.

Daniel Moon (D)

Department of Surgery, University of Melbourne, Melbourne, Australia.
Department of Urology, Royal Melbourne Hospital, Melbourne, Australia.

Phil Dundee (P)

Department of Urology, Royal Melbourne Hospital, Melbourne, Australia.

Niall Corcoran (N)

Department of Urology, Royal Melbourne Hospital, Melbourne, Australia.

Peter Carroll (P)

Department of Urology, University of California San Francisco, San Francisco, USA.

Alan Partin (A)

James Buchanan Brady Urological Institute, Johns Hopkins University, Baltimore, USA.

Joseph A Smith (JA)

Department of Urologic Surgery, Vanderbilt University, Nashville, USA.

Freddie Hamdy (F)

Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.

Caroline Moore (C)

Division of Surgery and Interventional Medicine, University College London, London, UK.

Piet Ost (P)

Radiation Oncology, Ghent University Hospital, Ghent, Belgium.

Tony Costello (T)

Department of Surgery, University of Melbourne, Melbourne, Australia.
Department of Urology, Royal Melbourne Hospital, Melbourne, Australia.

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