Population-based


Journal

Journal of medical genetics
ISSN: 1468-6244
Titre abrégé: J Med Genet
Pays: England
ID NLM: 2985087R

Informations de publication

Date de publication:
03 2023
Historique:
received: 17 02 2022
accepted: 17 05 2022
pubmed: 11 2 2023
medline: 3 3 2023
entrez: 10 2 2023
Statut: ppublish

Résumé

Ashkenazi Jewish (AJ) people have a higher incidence of We compared two population-based B-JFM screening programmes in Australia-using (1) an online tool (Sydney) and (2) in-person group sessions (Melbourne). Of 2167 Jewish people tested (Sydney n=594; Melbourne n=1573), 1.3% (n=28) have a B-JFM, only 2 of whom had a significant cancer family history (Manchester score ≥12). Pretest anxiety scores were normal (mean 9.9±3.5 (6-24)), with no significant post-result change (9.5±3.3). Decisional regret (mean 7.4±13.0 (0-100)), test-related distress (mean 0.8+/2.2 (0-30)) and positive experiences (reverse-scored) (mean 3.4±4.5 (1-20)) scores were low, with no significant differences between Sydney and Melbourne participants. Post-education knowledge was good overall (mean 11.8/15 (±2.9)) and significantly higher in Melbourne than Sydney. Post-result knowledge was the same (mean 11.7 (±2.4) vs 11.2 (±2.4)). Participants with a B-JFM had higher post-result anxiety and test-related distress and lower positive experiences, than those without a B-JFM, but scores were within the normal range. Family cancer history did not significantly affect knowledge or anxiety, or pretest perception of B-JFM or cancer risks. Most participants (93%) were satisfied/very satisfied with the programme. Both B-JFM screening programmes are highly acceptable to Australian Jewish communities. The programme enabled identification of several individuals who were previously unaware they have a B-JFM, many of whom would have been ineligible for current criteria-based testing in Australia.

Sections du résumé

BACKGROUND
Ashkenazi Jewish (AJ) people have a higher incidence of
METHODS
We compared two population-based B-JFM screening programmes in Australia-using (1) an online tool (Sydney) and (2) in-person group sessions (Melbourne).
RESULTS
Of 2167 Jewish people tested (Sydney n=594; Melbourne n=1573), 1.3% (n=28) have a B-JFM, only 2 of whom had a significant cancer family history (Manchester score ≥12). Pretest anxiety scores were normal (mean 9.9±3.5 (6-24)), with no significant post-result change (9.5±3.3). Decisional regret (mean 7.4±13.0 (0-100)), test-related distress (mean 0.8+/2.2 (0-30)) and positive experiences (reverse-scored) (mean 3.4±4.5 (1-20)) scores were low, with no significant differences between Sydney and Melbourne participants. Post-education knowledge was good overall (mean 11.8/15 (±2.9)) and significantly higher in Melbourne than Sydney. Post-result knowledge was the same (mean 11.7 (±2.4) vs 11.2 (±2.4)). Participants with a B-JFM had higher post-result anxiety and test-related distress and lower positive experiences, than those without a B-JFM, but scores were within the normal range. Family cancer history did not significantly affect knowledge or anxiety, or pretest perception of B-JFM or cancer risks. Most participants (93%) were satisfied/very satisfied with the programme.
CONCLUSION
Both B-JFM screening programmes are highly acceptable to Australian Jewish communities. The programme enabled identification of several individuals who were previously unaware they have a B-JFM, many of whom would have been ineligible for current criteria-based testing in Australia.

Identifiants

pubmed: 36763037
pii: jmedgenet-2022-108519
doi: 10.1136/jmedgenet-2022-108519
doi:

Substances chimiques

BRCA1 Protein 0
BRCA2 Protein 0
BRCA1 protein, human 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

265-273

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Jane M Tiller (JM)

Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Victorian Clinical Genetics Services, Parkville, Victoria, Australia.

Nicole E Cousens (NE)

Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
Hereditary Cancer Centre, Prince of Wales Hospital and Community Health Services, Randwick, New South Wales, Australia.

Rajneesh Kaur (R)

University of New South Wales, Sydney, New South Wales, Australia.
Sydney Medical School, The University of Sydney Faculty of Medicine and Health, Sydney, New South Wales, Australia.

Simone Rowley (S)

Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, Parkville, Victoria, Australia.

Yi-An Ko (YA)

Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, Parkville, Victoria, Australia.

Sakshi Mahale (S)

Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, Parkville, Victoria, Australia.

Agnes Bankier (A)

Royal Children's Hospital, Parkville, Victoria, Australia.

Bettina Meiser (B)

Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australia.

Kristine Barlow-Stewart (K)

The University of Sydney, Sydney, New South Wales, Australia.

Leslie Burnett (L)

Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.

Chris Jacobs (C)

Graduate School of Health, University of Technology Sydney, Sydney, New South Wales, Australia.

Paul James (P)

Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Genomic Medicine, Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Alison Trainer (A)

Parkville Familial Cancer Centre, Peter MacCallum Cancer Institute, Parkville, Victoria, Australia.
University of Melbourne, Melbourne, Victoria, Australia.

Suzanne Neil (S)

Epworth Hospital, Richmond, Victoria, Australia.

Ian G Campbell (IG)

Cancer Genetics Laboratory, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia.

Lesley Andrews (L)

University of New South Wales, Sydney, New South Wales, Australia.

Martin Delatycki (M)

Murdoch Children's Research Institute, Parkville, Victoria, Australia martin.delatycki@vcgs.org.au.
Victorian Clinical Genetics Services, Parkville, Victoria, Australia.

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Classifications MeSH