Evidence map›Paper›PMID 37202470›Full record

ArticleProstate cancer and prostatic diseases2024

Guidelines for genetic testing in prostate cancer: a scoping review.

Haitham Tuffaha, Kim Edmunds, David Fairbairn, Matthew J Roberts, Suzanne Chambers, David P Smith, Lisa Horvath, Shiksha Arora, Paul Scuffham

Open access · hybridAbstract readScoping Review
In one paragraph

Article in Prostate cancer and prostatic diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
10.1field-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.

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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

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  20. February 2025 Letters to the Editor.Clinical journal of oncology nursing · 2025
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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

9 authors at 5 institutions in 1 country.

Haitham TuffahaCentre for the Business and Economics of Health, University of Queensland, Brisbane, QLD, Australia. h.tuffaha@uq.edu.au.ORCID 0000-0003-2993-3480
Kim EdmundsCentre for the Business and Economics of Health, University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0001-7379-1294
David FairbairnPathology Queensland, The Royal Brisbane Women's Hospital, Brisbane, QLD, Australia.
Matthew J RobertsUQ Centre for Clinical Research, University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0003-0552-7402
Suzanne ChambersThe Faculty of Health Sciences, Australian Catholic University, Brisbane, NSW, Australia.
David P SmithThe Daffodil Centre, The University of Sydney, A Joint Venture with Cancer Council NSW, Sydney, NSW, Australia.ORCID 0000-0002-1474-3214
Lisa HorvathMedical Oncology, Chris O'Brien Lifehouse, Camperdown, NSW, Australia.ORCID 0000-0001-6842-9223
Shiksha AroraCentre for the Business and Economics of Health, University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0003-3098-4584
Paul ScuffhamMenzies Health Institute Queensland, Griffith University, Gold Coast, QLD, Australia.ORCID 0000-0001-5931-642X
The University of Queensland · AUThe University of Sydney · AUAustralian Catholic University · AUGriffith University · AURoyal Brisbane and Women's Hospital · AU

Funding

Prostate Cancer Foundation of Australia (PCFA) PIRA FLECR-3421
6 · The paper itself

Abstract

backgroundGenetic testing, to identify pathogenic or likely pathogenic variants in prostate cancer, is valuable in guiding treatment decisions for men with prostate cancer and to inform cancer prevention and early detection options for their immediate blood relatives. There are various guidelines and consensus statements for genetic testing in prostate cancer. Our aim is to review genetic testing recommendations across current guidelines and consensus statements and the level of evidence supporting those recommendations.

methodsA scoping review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-analyses extension for scoping review (PRISMA-ScR) guidelines. Electronic database searches and manual searches of grey literature, including websites of key organisations were conducted. Using the Population, Concept, Context (PCC) framework, this scoping review included: men with prostate cancer or men at high risk of prostate cancer and their biological families; existing guidelines and consensus statements with supporting evidence for genetic testing of men with prostate cancer from any geographical location worldwide.

resultsOf the 660 citations identified, 23 guidelines and consensus statements met the inclusion criteria for the scoping review. Based on different levels of evidence about who should be tested and how, a diverse range of recommendations were identified. There was general consensus among the guidelines and consensus statements that men with metastatic disease be offered genetic testing; however, there was less consensus in relation to genetic testing in localised prostate cancer. While there was some consensus in relation to which genes to test, recommendations varied regarding who to test, testing methods and implementation.

conclusionWhile genetic testing in prostate cancer is routinely recommended and numerous guidelines exist, there is still considerable lack of consensus regarding who should be tested and how they should be tested. Further evidence is needed to inform value-based genetic testing strategies for implementation in practice.

Indexed as

Genetic TestingPractice Guidelines as TopicProstatic NeoplasmsEarly Detection of CancerGenetic Predisposition to DiseaseHumansMale

Identifiers

PMID37202470
PMCPMC11543603
OpenAlexW4377047115

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.