Survey on Physicians' Knowledge and Training Needs in Genetic Counseling in Germany.

BRCA1/BRCA2 mutations Genetic counseling Genetic testing Hereditary breast cancer

Journal

Breast care (Basel, Switzerland)
ISSN: 1661-3791
Titre abrégé: Breast Care (Basel)
Pays: Switzerland
ID NLM: 101254060

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 05 03 2020
accepted: 25 08 2020
entrez: 4 10 2021
pubmed: 5 10 2021
medline: 5 10 2021
Statut: ppublish

Résumé

In recent years, germline testing of women with a risk of developing breast and ovarian cancer has increased rapidly. This is due to lower costs for new high-throughput sequencing technologies and the manifold preventive and therapeutic options for germline mutation carriers. The growing demand for genetic counseling meets a shortfall of counselors and illustrates the need to involve the treating clinicians in the genetic testing process. This survey was undertaken to assess their state of knowledge and training needs in the field of genetic counseling and testing. A cross-sectional survey within the European Bridges Study (Breast Cancer Risk after Diagnostic Gene Sequencing) was conducted among physician members ( Overall, the study revealed a need for training in risk communication and clinical recommendations for persons at risk. One-third of respondents communicated only relative disease risks (31.5%) instead of absolute disease risks in manageable time spans. Moreover, almost one-third of the respondents (31.2%) communicated bilateral and contralateral risk-reducing mastectomy as an option for healthy women and unilateral-diseased breast cancer patients without mutations in high-risk genes (e.g. The survey demonstrates a gap of genetic and risk literacy in a relevant proportion of physicians and the need for appropriate training concepts.

Sections du résumé

BACKGROUND BACKGROUND
In recent years, germline testing of women with a risk of developing breast and ovarian cancer has increased rapidly. This is due to lower costs for new high-throughput sequencing technologies and the manifold preventive and therapeutic options for germline mutation carriers. The growing demand for genetic counseling meets a shortfall of counselors and illustrates the need to involve the treating clinicians in the genetic testing process. This survey was undertaken to assess their state of knowledge and training needs in the field of genetic counseling and testing.
METHODS METHODS
A cross-sectional survey within the European Bridges Study (Breast Cancer Risk after Diagnostic Gene Sequencing) was conducted among physician members (
RESULTS RESULTS
Overall, the study revealed a need for training in risk communication and clinical recommendations for persons at risk. One-third of respondents communicated only relative disease risks (31.5%) instead of absolute disease risks in manageable time spans. Moreover, almost one-third of the respondents (31.2%) communicated bilateral and contralateral risk-reducing mastectomy as an option for healthy women and unilateral-diseased breast cancer patients without mutations in high-risk genes (e.g.
CONCLUSION CONCLUSIONS
The survey demonstrates a gap of genetic and risk literacy in a relevant proportion of physicians and the need for appropriate training concepts.

Identifiants

pubmed: 34602945
doi: 10.1159/000511136
pii: brc-0016-0389
pmc: PMC8436720
doi:

Types de publication

Journal Article

Langues

eng

Pagination

389-395

Informations de copyright

Copyright © 2020 by S. Karger AG, Basel.

Déclaration de conflit d'intérêts

The authors declare there are no conflicts of interest.

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Auteurs

Julia Dick (J)

Center for Hereditary Breast and Ovarian Cancer and Center for Integrated Oncology (CIO), Medical Faculty, University Hospital Cologne, Cologne, Germany.

Viktoria Aue (V)

Center for Hereditary Breast and Ovarian Cancer and Center for Integrated Oncology (CIO), Medical Faculty, University Hospital Cologne, Cologne, Germany.

Simone Wesselmann (S)

German Cancer Society (DKG), Berlin, Germany.

Anne Brédart (A)

Supportive Care Department, Psycho-Oncology Unit, Institut Curie, Paris, France.
University Paris Descartes, Boulogne-Billancourt, France.

Sylvie Dolbeault (S)

Supportive Care Department, Psycho-Oncology Unit, Institut Curie, Paris, France.
Centre de Recherche en Épidémiologie et Santé des Populations (CESP), University Paris-Sud, UVSQ, INSERM, University Paris-Saclay, Villejuif Cedex, France.

Peter Devilee (P)

Departments of Human Genetics and Pathology, Leiden University Medical Centre, Leiden, The Netherlands.

Dominique Stoppa-Lyonnet (D)

Cancer Genetic Clinic, Institut Curie, Paris, France.

Rita K Schmutzler (RK)

Center for Hereditary Breast and Ovarian Cancer and Center for Integrated Oncology (CIO), Medical Faculty, University Hospital Cologne, Cologne, Germany.

Kerstin Rhiem (K)

Center for Hereditary Breast and Ovarian Cancer and Center for Integrated Oncology (CIO), Medical Faculty, University Hospital Cologne, Cologne, Germany.

Classifications MeSH