Claus Elizabeth B, Petruzella Stacey, Matloff Ellen, Carter Darryl
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Conn 06520-8034, USA.
JAMA. 2005 Feb 23;293(8):964-9. doi: 10.1001/jama.293.8.964.
The distribution of BRCA1 and BRCA2 mutations in women diagnosed with noninvasive breast carcinoma is unknown.
To estimate the BRCA1 and BRCA2 mutation prevalence in women with ductal carcinoma in situ (DCIS), unselected for age, family history, or ethnicity.
DESIGN, SETTING, AND PARTICIPANTS: The data were 369 DCIS cases diagnosed among female residents aged 20 to 79 years from the state of Connecticut between September 15, 1994, and March 14, 1998. These women were participants in a large population-based case-control study of breast carcinoma in situ. Telephone interviews were used to collect risk factor information and blood or buccal specimens were collected for BRCA1 and BRCA2 mutation testing.
Prevalence of disease-associated mutations of BRCA1 and BRCA2 in women diagnosed with DCIS.
Three (0.8%) and 9 (2.4%) of 369 DCIS cases had disease-associated mutations in BRCA1 or BRCA2, respectively. One woman had a mutation in both genes (BRCA1 W321X and BRCA2 3398del5). Carriers were significantly more likely than noncarriers to report a first-degree (mother, sister, or daughter) family history of breast cancer (odds ratio [OR], 3.7; 95% confidence interval [CI], 1.1-12.4), as well as a personal history of ovarian cancer. In addition, carriers were more likely than noncarriers to be diagnosed at an early age (<50 years) (OR, 3.4; 95% CI, 1.0-11.7), as well as to report at least 1 first-degree relative diagnosed with breast cancer before 50 years (OR, 10.6; 95% CI, 3.0-37.0).
Ductal carcinoma in situ is a part of the breast/ovarian cancer syndromes defined by BRCA1 and BRCA2, with mutation rates similar to those found for invasive breast cancer. These findings suggest that patients with breast cancer with an appropriate personal or family history of breast and/or ovarian cancer should be screened and followed according to high-risk protocols, regardless of whether they are diagnosed with in situ or invasive breast cancer.
被诊断为非浸润性乳腺癌的女性中BRCA1和BRCA2突变的分布情况尚不清楚。
评估未按年龄、家族史或种族进行选择的导管原位癌(DCIS)女性中BRCA1和BRCA2突变的患病率。
设计、地点和参与者:数据来自1994年9月15日至1998年3月14日期间在康涅狄格州诊断出的369例年龄在20至79岁之间的女性DCIS病例。这些女性是一项基于人群的大型原位乳腺癌病例对照研究的参与者。通过电话访谈收集危险因素信息,并采集血液或口腔拭子样本进行BRCA1和BRCA2突变检测。
被诊断为DCIS的女性中BRCA1和BRCA2疾病相关突变的患病率。
369例DCIS病例中,分别有3例(0.8%)和9例(2.4%)在BRCA1或BRCA2中有疾病相关突变。一名女性两个基因均有突变(BRCA1 W321X和BRCA2 3398del5)。与非携带者相比,携带者报告乳腺癌一级(母亲、姐妹或女儿)家族史(优势比[OR],3.7;95%置信区间[CI],1.1 - 12.4)以及卵巢癌个人史的可能性显著更高。此外,与非携带者相比,携带者在早年(<50岁)被诊断出的可能性更大(OR,3.4;95% CI,1.0 - 11.7),并且报告至少有一名50岁之前被诊断出乳腺癌的一级亲属的可能性也更大(OR,10.6;95% CI,3.0 - 37.0)。
导管原位癌是由BRCA1和BRCA2定义的乳腺/卵巢癌综合征的一部分,其突变率与浸润性乳腺癌相似。这些发现表明,有适当的个人或家族性乳腺和/或卵巢癌病史的乳腺癌患者,无论其被诊断为原位癌还是浸润性乳腺癌,都应按照高危方案进行筛查和随访。