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. 2019 Aug 1;111(8):795-802.
doi: 10.1093/jnci/djz008.

Trends in BRCA Test Utilization in an Integrated Health System, 2005-2015

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Trends in BRCA Test Utilization in an Integrated Health System, 2005-2015

Sarah Knerr et al. J Natl Cancer Inst. .

Abstract

Background: Genetic testing to determine BRCA status has been available for over two decades, but there are few population-based studies of test diffusion. We report 10-year trends in BRCAtesting in an integrated health-care system with long-standing access to genetic services.

Methods: A cohort of women aged 18 years and older was created to ascertain BRCA testing (n = 295 087). Annual testing rates between 2005 and 2015 were calculated in all women with and without incident (ie, newly diagnosed) breast and ovarian cancers and in clinically eligible subgroups by family cancer history, personal cancer history, and age at diagnosis. Secular trends were assessed using Poisson regression. Women tested early (2005-2008), midway (2009-2012), and late (2013-2015) in the study period were compared in cross-sectional analyses.

Results: Between 2005 and 2015, annual testing rates increased from 0.6/1000 person-years (pys) (95% confidence interval [CI] = 0.4 to 0.7/1000 pys) to 0.8/1000 pys (95% CI = 0.6 to 1.0/1000 pys) in women without incident breast or ovarian cancers. Rates decreased from 71.5/1000 pys (95% CI = 42.4 to 120.8/1000 pys) to 44.4/1000 pys (95% CI = 35.5 to 55.6/1000 pys) in women with incident diagnoses, despite improvements in provision of timely BRCA testing during this time frame. We found no evidence of secular trends in clinically eligible subgroups including women with family history indicating increased hereditary cancer risk, but no personal cancer history. At the end of the study period, 97.0% (95% CI = 96.6% to 97.3%) of these women remained untested.

Conclusion: Many eligible women did not receive BRCA testing despite having insurance coverage and access to specialty genetic services, underscoring challenges to primary and secondary hereditary cancer prevention.

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Figures

Figure 1.
Figure 1.
Personal and family cancer history and contributed person-time for three hypothetical women. BC = breast cancer; BCSC = Breast Cancer Surveillance Consortium; D = death; DX = diagnosis; E = study entry; OC = ovarian cancer; T = BRCA test; SEER = Surveillance, Epidemiology, and End Results Registry.
Figure 2.
Figure 2.
Annual BRCAtesting rates in women with and without incident breast and ovarian cancer diagnoses, 2005–2015. Error bars indicate 95% confidence intervals for annual rates. BC = breast cancer; OC = ovarian cancer.

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References

    1. Turnbull C, Rahman N. Genetic predisposition to breast cancer: past, present, and future. Annu Rev Genomics Hum Genet. 2008;91:321–345. - PubMed
    1. Norquist BM, Harrell MI, Brady MF et al. . Inherited mutations in women with ovarian carcinoma. JAMA Oncol. 2016;24:482–490. - PMC - PubMed
    1. Chen S, Parmigiani G. Meta-analysis of BRCA1 and BRCA2 penetrance. J Clin Oncol. 2007;2511:1329–1333. - PMC - PubMed
    1. Antoniou A, Pharoah PD, Narod S et al. . Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet. 2003;725:1117–1130. - PMC - PubMed
    1. Kuchenbaecker KB, Hopper JL, Barnes DR et al. . Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers. JAMA. 2017;31723:2402–2416. - PubMed

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