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BRCA1 和 BRCA2 基因突变携带者中导管原位癌的外显率。

The penetrance of ductal carcinoma in situ among BRCA1 and BRCA2 mutation carriers.

机构信息

Department of Biostatistics, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215-5450, USA.

出版信息

Breast Cancer Res Treat. 2013 Jan;137(1):315-8. doi: 10.1007/s10549-012-2345-5. Epub 2012 Nov 27.

Abstract

Ductal carcinoma in situ (DCIS) is a precancerous lesion of the female breast and is strongly suspected to be a precursor of invasive breast cancer (IBC). Our goal is the estimation of the age-specific and lifetime penetrances of DCIS among carriers of either a BRCA1 or BRCA2 deleterious mutation. We jointly re-analyze the SEER9 database and a previous study by Claus et al. (JAMA 293:964-969, 2005). Estimation is performed via Bayes theorem after the evaluation of the ratio of age-specific DCIS incidences, and extrapolation to the general population of the study-specific penetrance obtained from Claus et al. From the SEER9 database, we estimate the lifetime risk of DCIS to be 0.98 %, in contrast to value of 12.5 % usually reported for IBC. By extending the result in Claus et al. to the general population, we obtain a lifetime risk for carriers of a deleterious mutation of either BRCA1 or BRCA2 of 6.21 % (95 % CI 6.09-6.33 %). The increase in lifetime risk of DCIS for a BRCA mutation carrier compared to a non-carrier is therefore about six-fold. Our quantification is directly relevant to the identification and genetic counseling of BRCA mutation carriers, and emphasizes the potential importance of including information on diagnoses of DCIS in counseling of individuals who are at familial risk for breast cancer. All these factors can contribute to a more specific and targeted prevention, potentially reducing the impact of IBC among BRCA mutation carriers.

摘要

导管原位癌(DCIS)是女性乳腺癌的癌前病变,强烈怀疑是浸润性乳腺癌(IBC)的前身。我们的目标是估计 BRCA1 或 BRCA2 有害突变携带者中 DCIS 的年龄特异性和终生外显率。我们联合重新分析了 SEER9 数据库和 Claus 等人之前的研究(JAMA 293:964-969, 2005)。通过评估年龄特异性 DCIS 发病率的比值,在评估 Claus 等人从特定研究中获得的外显率后,通过贝叶斯定理进行估计,并外推到研究人群中的一般人群。从 SEER9 数据库中,我们估计 DCIS 的终生风险为 0.98%,而通常报告的 IBC 的终生风险为 12.5%。通过将 Claus 等人的结果扩展到一般人群,我们获得了 BRCA1 或 BRCA2 有害突变携带者的终生风险为 6.21%(95%CI 6.09-6.33%)。与非携带者相比,BRCA 突变携带者的 DCIS 终生风险增加了约六倍。我们的定量分析直接关系到 BRCA 突变携带者的识别和遗传咨询,强调了在对乳腺癌家族风险个体进行咨询时纳入 DCIS 诊断信息的潜在重要性。所有这些因素都有助于更具体和有针对性的预防,可能会降低 BRCA 突变携带者中 IBC 的影响。

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本文引用的文献

1
Variation of breast cancer risk among BRCA1/2 carriers.
JAMA. 2008 Jan 9;299(2):194-201. doi: 10.1001/jama.2007.55-a.
2
Meta-analysis of BRCA1 and BRCA2 penetrance.
J Clin Oncol. 2007 Apr 10;25(11):1329-33. doi: 10.1200/JCO.2006.09.1066.
3
BayesMendel: an R environment for Mendelian risk prediction.
Stat Appl Genet Mol Biol. 2004;3:Article21. doi: 10.2202/1544-6115.1063. Epub 2004 Sep 17.
4
Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ.
JAMA. 2005 Feb 23;293(8):964-9. doi: 10.1001/jama.293.8.964.
5
The BOADICEA model of genetic susceptibility to breast and ovarian cancer.
Br J Cancer. 2004 Oct 18;91(8):1580-90. doi: 10.1038/sj.bjc.6602175.
6
A breast cancer prediction model incorporating familial and personal risk factors.
Stat Med. 2004 Apr 15;23(7):1111-30. doi: 10.1002/sim.1668.
7
Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.
Science. 2003 Oct 24;302(5645):643-6. doi: 10.1126/science.1088759.
9
Population-based study of risk of breast cancer in carriers of BRCA2 mutation.
Lancet. 1998 Oct 24;352(9137):1337-9. doi: 10.1016/s0140-6736(98)03300-5.

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