Evidence map›Paper›PMID 42032667›Full record

ArticleHereditary cancer in clinical practice2026

Breast cancer specialists' experiences and attitudes towards mainstream genetic testing for patients with breast cancer.

Kirsten Allan, Linda Cicciarelli, Catherine Beard, Geoffrey J Lindeman, G Bruce Mann, Paul A James, Laura E Forrest

Abstract read
In one paragraph

Article in Hereditary cancer in clinical practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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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

7 authors.

Kirsten AllanDepartment of Paediatrics, The University of Melbourne, Parkville, 3010, Australia.
Linda CicciarelliParkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Catherine BeardParkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Geoffrey J LindemanParkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
G Bruce MannDepartment of Surgery, The University of Melbourne, Parkville, 3010, Australia.
Paul A JamesParkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
Laura E ForrestParkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia. laura.forrest@petermac.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGermline genetic testing is an increasingly important component of treatment decision-making for clinicians and patients with breast cancer. To address increased demand and expedite access to genetic testing for these patients, the Parkville Familial Cancer Centre (PFCC) in Victoria, Australia, implemented a breast mainstream genetic testing program. The program educates and supports breast cancer specialists to provide eligible patients with pre-test information, gain consent, and arrange genetic testing during their routine cancer appointments. This study aimed to explore breast cancer specialists’ experiences and opinions of the education program and of facilitating mainstream genetic testing for their patients.

methodsSpecialists who had attended the mainstream genetic testing education were invited to complete an online survey about the training provided through the education program and their experience of deploying mainstream genetic testing in their practice. Descriptive statistics were compiled, and content analysis used for open text responses.

resultsForty-five breast cancer specialists (breast surgeons, medical oncologists, radiation oncologists and breast care nurses) responded (45% response rate). Most respondents had discussed (87%) and consented (80%) patients for mainstream genetic testing. Most specialists (81%) rated their confidence levels as high or very high for consenting patients to mainstream genetic testing. The majority (89%) indicated that they believed mainstream genetic testing should be part of their role and felt well supported by the PFCC (90%).

conclusionBreast cancer specialists used the education they received in the mainstream education program and were supported to deliver mainstream breast cancer genetic testing to their patients.

Indexed as

AttitudesBreast cancerGenetic testingMainstreamingOncologyOncology professionals

Identifiers

PMID42032667
PMCPMC13262353

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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.