Evidence map›Paper›PMID 39402389›Full record

ArticleEuropean journal of human genetics : EJHG2024

Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres.

Cristina Fortuno, Elisa J Cops, Aimee L Davidson, Johanna Hadler, Giovanni Innella, Maddison E McKenzie, Michael Parsons, Ainsley M Campbell, Andrew Dubowsky, Verna Fargas and 16 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2024. 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

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

1 citing paper in PubMed.

  1. New guidelines for rare cancer syndromes.European journal of human genetics : EJHG · 2024
    Article
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

26 authors.

Cristina FortunoPopulation Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Elisa J CopsParkville Familial Cancer Centre, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, VIC, Australia.
Aimee L DavidsonPopulation Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.ORCID 0000-0001-5034-5996
Johanna HadlerPopulation Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Giovanni InnellaDipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy.ORCID 0000-0002-6909-2412
Maddison E McKenziePopulation Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Michael ParsonsPopulation Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.ORCID 0000-0003-3242-8477
Ainsley M CampbellDepartment of Clinical Genetics, Austin Health, Melbourne, VIC, Australia.
Andrew DubowskyDepartment of Genetics and Molecular Pathology, SA Pathology, Adelaide, SA, Australia.ORCID 0000-0002-9585-1136
Verna FargasLiverpool Cancer Genetics, Liverpool Hospital, Liverpool, NSW, Australia.
Michael J FieldFamily Cancer Clinic, Royal North Shore Hospital, St Leonards, NSW, Australia.ORCID 0000-0001-7455-934X
Helen G Mar FanGenetic Health Queensland Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Cassandra B NicholsGenetic Health WA, King Edward Memorial Hospital, Perth, WA, Australia.
Nicola K PoplawskiAdult Genetics Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.ORCID 0000-0002-9372-3325
Linda WarwickACT Genetic Service Canberra Health Services, Garran, ACT, Australia.
Rachel WilliamsSchool of Clinical Medicine, UNSW Medicine & Health, UNSW Sydney, Sydney, NSW, Australia.
Victoria BeshayPeter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Caitlin EdwardsDiagnostic Genomics, Pathwest Laboratory Medicine, QEII Medical Centre, Nedlands, WA, Australia.
Andrea JohnsNSW Health Pathology, Newcastle, NSW, Australia.
Mary McPhillipsNSW Health Pathology, Newcastle, NSW, Australia.
Vanessa Siva KumarInvitae Australia, Sydney, NSW, Australia.
Rodney ScottNSW Health Pathology, Newcastle, NSW, Australia.
Mark WilliamsGenomic Diagnostics, Melbourne, VIC, Australia.ORCID 0000-0002-1294-1110
Hamish ScottDepartment of Genetics and Molecular Pathology, SA Pathology, Adelaide, SA, Australia.ORCID 0000-0002-5813-631X
Paul A JamesParkville Familial Cancer Centre, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, VIC, Australia.ORCID 0000-0002-4361-4657
Amanda B SpurdlePopulation Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. amanda.spurdle@qimrberghofer.edu.au.ORCID 0000-0003-1337-7897

Funding

Department of Health | National Health and Medical Research Council (NHMRC) APP177524National Breast Cancer Foundation (NBCF) IIRS-21-102
6 · The paper itself

Abstract

Breast cancer remains a significant global health challenge. In Australia, the adoption of publicly-funded multigene panel testing for eligible cancer patients has increased accessibility to personalised care, yet has also highlighted the increasing prevalence of variants of uncertain significance (VUS), complicating clinical decision-making. This project aimed to explore the spectrum and actionability of breast cancer VUS in Australian familial cancer centers (FCCs). Leveraging data from 11 FCCs participating in the Inherited Cancer Connect database, we retrieved VUS results from 1472 patients. Through ClinVar crosschecks and application of gene-specific ACMG/AMP guidelines, we showed the potential for reclassification of 4% of unique VUS as pathogenic or likely pathogenic, and 80% as benign or likely benign. Surveys conducted with FCCs and diagnostic laboratories described current practices and challenges in variant reclassifications, highlighting resource constraints preventing periodic VUS review and notifications from the laboratories to the FCCs. Our study suggests there are benefits to routine VUS review and reclassification, particularly in publicly-funded healthcare systems. Future research should focus on assessing the clinical impact and cost-effectiveness of implementing routine variant review practices, alongside efforts to enhance communication between FCCs and laboratories.

Indexed as

Breast NeoplasmsGenetic TestingAustraliaFemaleGenetic Predisposition to DiseaseHumans

Identifiers

PMID39402389
PMCPMC11607406

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.