Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Jun 30;29(7):4632-4646.
doi: 10.3390/curroncol29070368.

Gynecologic Cancer Risk and Genetics: Informing an Ideal Model of Gynecologic Cancer Prevention

Affiliations
Review

Gynecologic Cancer Risk and Genetics: Informing an Ideal Model of Gynecologic Cancer Prevention

Lauren C Tindale et al. Curr Oncol. .

Abstract

Individuals with proven hereditary cancer syndrome (HCS) such as BRCA1 and BRCA2 have elevated rates of ovarian, breast, and other cancers. If these high-risk people can be identified before a cancer is diagnosed, risk-reducing interventions are highly effective and can be lifesaving. Despite this evidence, the vast majority of Canadians with HCS are unaware of their risk. In response to this unmet opportunity for prevention, the British Columbia Gynecologic Cancer Initiative convened a research summit "Gynecologic Cancer Prevention: Thinking Big, Thinking Differently" in Vancouver, Canada on 26 November 2021. The aim of the conference was to explore how hereditary cancer prevention via population-based genetic testing could decrease morbidity and mortality from gynecologic cancer. The summit invited local, national, and international experts to (1) discuss how genetic testing could be more broadly implemented in a Canadian system, (2) identify key research priorities in this topic and (3) outline the core essential elements required for such a program to be successful. This report summarizes the findings from this research summit, describes the current state of hereditary genetic programs in Canada, and outlines incremental steps that can be taken to improve prevention for high-risk Canadians now while developing an organized population-based hereditary cancer strategy.

Keywords: BRCA; cancer screening; hereditary cancer syndrome; population-based genetic testing.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Actionable steps towards hereditary ovarian cancer prevention. The upper dashed line represents the ~20% of hereditary ovarian cancer cases that are attributed to BRCA1 and BRCA2 mutations.
Figure 2
Figure 2
Research summit participants were asked to rate statements about hereditary cancer prevention using the following scale: strongly disagree, disagree, neither agree nor disagree, agree, or strongly agree.
Figure 3
Figure 3
Research summit participants were asked to assign a priority rating to hereditary cancer prevention action items using the following scale: low priority, medium priority, high priority, or very high priority.

Similar articles

Cited by

References

    1. Toss A., Tomasello C., Razzaboni E., Contu G., Grandi G., Cagnacci A., Schilder R.J., Cortesi L. Hereditary Ovarian Cancer: Not Only BRCA 1 and 2 Genes. BioMed Res. Int. 2015;2015:341723. doi: 10.1155/2015/341723. - DOI - PMC - PubMed
    1. Chen X., Jiang J., Shen H., Hu Z. Genetic Susceptibility of Cervical Cancer. J. Biomed. Res. 2011;25:155. doi: 10.1016/S1674-8301(11)60020-1. - DOI - PMC - PubMed
    1. Trietsch M.D., Nooij L.S., Gaarenstroom K.N., Van Poelgeest M.I.E. Genetic and Epigenetic Changes in Vulvar Squamous Cell Carcinoma and Its Precursor Lesions: A Review of the Current Literature. Gynecol. Oncol. 2015;136:143–157. doi: 10.1016/j.ygyno.2014.11.002. - DOI - PubMed
    1. Kuchenbaecker K.B., Hopper J.L., Barnes D.R., Phillips K.-A., Mooij T.M., Roos-Blom M.-J., Jervis S., van Leeuwen F.E., Milne R.L., Andrieu N., et al. Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers. JAMA. 2017;317:2402–2416. doi: 10.1001/jama.2017.7112. - DOI - PubMed
    1. Li J., Wen W.X., Eklund M., Kvist A., Eriksson M., Christensen H.N., Torstensson A., Bajalica-Lagercrantz S., Dunning A.M., Decker B., et al. Prevalence of BRCA1 and BRCA2 Pathogenic Variants in a Large, Unselected Breast Cancer Cohort. Int. J. Cancer. 2019;144:1195–1204. doi: 10.1002/ijc.31841. - DOI - PMC - PubMed

Publication types

LinkOut - more resources