Evidence map›Paper›PMID 36029389›Full record

ArticleFamilial cancer2023

A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland.

Terri Patricia McVeigh, Karl J Sweeney, Donal J Brennan, Una M McVeigh, Simon Ward, Ann Strydom, Sheila Seal, Katherine Astbury, Paul Donnellan, Joanne Higgins and 27 more

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Article in Familial cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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

37 authors at 11 institutions in 2 countries.

Terri Patricia McVeighCancer Genetics Unit, Royal Marsden NHS Foundation Trust, London, UK. Terri.McVeigh@rmh.nhs.uk.ORCID 0000-0001-9201-9216
Karl J SweeneySaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Donal J BrennanMater Misericordiae University Hospital, Dublin, Ireland.
Una M McVeighNational University of Ireland, Galway, Ireland.
Simon WardCancer Genetics Unit, Royal Marsden NHS Foundation Trust, London, UK.
Ann StrydomTGL Clinical Laboratory, Sutton, UK.
Sheila SealTGL Clinical Laboratory, Sutton, UK.
Katherine AstburySaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Paul DonnellanSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Joanne HigginsSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Maccon KeaneSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Michael J KerinSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Carmel MaloneSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Pauline McGoughSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Ray McLaughlinSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Michael O'LearySaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Margaret RusheSaolta Health Care Group, Galway University Hospital, Galway, Ireland.
Michael Kevin BarrySaolta Health Care Group, Mayo University Hospital, Co Mayo, Castlebar, Ireland.
Geraldine MacGregorSaolta University Health Care Group, Letterkenny University Hospital, Co Donegal, Letterkenny, Ireland.
Michael SugrueSaolta University Health Care Group, Letterkenny University Hospital, Co Donegal, Letterkenny, Ireland.
Ala YousifSaolta University Hospital Group, Sligo University Hospital, Sligo, Ireland.
Dhafir Al-AzawiSt James's University Hospital, Dublin, Ireland.
Eileen BerkeleySt James's University Hospital, Dublin, Ireland.
Terence J BoyleSt James's University Hospital, Dublin, Ireland.
Elizabeth M ConnollySt James's University Hospital, Dublin, Ireland.
Carmel NolanSt James's University Hospital, Dublin, Ireland.
Elaine RichardsonSt James's University Hospital, Dublin, Ireland.
Claire GiffneyChildren's Health Ireland at Crumlin, Dublin, Ireland.
Samantha B DoyleThe National Maternity Hospital, Holles St, Dublin, Ireland.
Sheila BroderickMater Misericordiae University Hospital, Dublin, Ireland.
William BoydMater Misericordiae University Hospital, Dublin, Ireland.
Ruaidhri McVeyMater Misericordiae University Hospital, Dublin, Ireland.
Thomas WalshMater Misericordiae University Hospital, Dublin, Ireland.
Michael FarrellMater Private Hospital, Dublin, Ireland.
David J GallagherSt James's University Hospital, Dublin, Ireland.
Nazneen RahmanTGL Clinical Laboratory, Sutton, UK.
Angela J GeorgeCancer Genetics Unit, Royal Marsden NHS Foundation Trust, London, UK.
University Hospital Galway · IEMater Misericordiae University Hospital · IESt. James's Hospital · IEOllscoil na Gaillimhe – University of Galway · IERoyal Marsden NHS Foundation Trust · GBSutton Hospital · GBLetterkenny University Hospital · IEChildren's Health Ireland at Crumlin · IEMayo General Hospital · IENational Maternity Hospital · IESligo University Hospital · IE

Funding

Wellcome Trust 098518
6 · The paper itself

Abstract

In the Republic of Ireland (ROI), BRCA1/BRCA2 genetic testing has been traditionally undertaken in eligible individuals, after pre-test counselling by a Clinical Geneticist/Genetic Counsellor. Clinical Genetics services in ROI are poorly resourced, with routine waiting times for appointments at the time of this pilot often extending beyond a year. The consequent prolonged waiting times are unacceptable where therapeutic decision-making depends on the patient's BRCA status. "Mainstreaming" BRCA1/BRCA2 testing through routine oncology/surgical clinics has been implemented successfully in other centres in the UK and internationally. We aimed to pilot this pathway in three Irish tertiary centres. A service evaluation project was undertaken over a 6-month period between January and July 2017. Eligible patients, fulfilling pathology and age-based inclusion criteria defined by TGL clinical, were identified, and offered constitutional BRCA1/BRCA2 testing after pre-test counselling by treating clinicians. Tests were undertaken by TGL Clinical. Results were returned to clinicians by secure email. Onward referrals of patients with uncertain/pathogenic results, or suspicious family histories, to Clinical Genetics were made by the treating team. Surveys assessing patient and clinician satisfaction were sent to participating clinicians and a sample of participating patients. Data was collected with respect to diagnostic yield, turnaround time, onward referral rates, and patient and clinician feedback. A total of 101  patients underwent diagnostic germline BRCA1/BRCA2 tests through this pathway. Pathogenic variants were identified in 12 patients (12%). All patients in whom variants were identified were appropriately referred to Clinical Genetics. At least 12 additional patients with uninformative BRCA1/BRCA2 tests were also referred for formal assessment by Clinical Geneticist or Genetic Counsellor. Issues were noted in terms of time pressures and communication of results to patients. Results from a representative sample of participants completing the satisfaction survey indicated that the pathway was acceptable to patients and clinicians. Mainstreaming of constitutional BRCA1/BRCA2 testing guided by age- and pathology-based criteria is potentially feasible for patients with breast cancer as well as patients with ovarian cancer in Ireland.

Indexed as

Breast NeoplasmsOvarian NeoplasmsBRCA1 ProteinBRCA2 ProteinFeasibility StudiesFemaleGenetic Predisposition to DiseaseGenetic TestingGerm-Line MutationHumansIrelandPilot ProjectsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBRCA1BRCA2Breast cancerCancer geneticsCancer genomicsHereditary Breast and Ovarian cancerKing syndromeMainstreamingOncogeneticsOvarian cancer

Identifiers

PMID36029389
OpenAlexW4293421926

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Registered trials

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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.