Atchley Deann P, Albarracin Constance T, Lopez Adriana, Valero Vicente, Amos Christopher I, Gonzalez-Angulo Ana Maria, Hortobagyi Gabriel N, Arun Banu K
Department of Breast Medical Oncology, Unit 1354, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.
J Clin Oncol. 2008 Sep 10;26(26):4282-8. doi: 10.1200/JCO.2008.16.6231.
Mutations in the BRCA1 and BRCA2 genes confer greater risk of developing breast cancer. We determined whether tumor pathologic features and clinical features differ in patients with and without BRCA mutations.
Tumor pathologic features and clinical characteristics were examined in 491 women with breast cancer who underwent genetic testing for BRCA mutations between 1997 and 2006. A retrospective review of medical records was conducted to determine clinical characteristics including ethnicity, age and clinical stage at diagnosis, age at parity, number of full-term pregnancies, use of oral contraceptives and hormone replacement therapy, and BRCA mutation status. Tumor pathology was reviewed to determine histologic type, tumor grade, and estrogen receptor, progesterone receptor, and HER-2/neu status.
Of the 491 patients with identified breast cancers, 391 patients were BRCA negative, and 86 patients were BRCA positive. Triple-negative breast cancer (ie, those with negative estrogen receptor, progesterone receptor, and HER-2/neu status) was diagnosed in 57.1% of the BRCA1-positive patients, 23.3% of the BRCA2-positive patients, and 13.8% of the BRCA-negative patients. BRCA1 mutation carriers had higher nuclear grade tumors than the other two groups (P < .001). Of the triple-negative cancer patients, BRCA2 mutation carriers were older when diagnosed than BRCA1 mutation carriers and noncarriers (P < .01).
These results suggest that tumors associated with BRCA1 mutations may be divided into two distinct groups, triple-negative and non-triple-negative groups. Future studies should seek to determine whether patients with BRCA1 mutations and triple-negative breast cancer respond to treatment better than BRCA-negative patients with similar tumor pathology.
BRCA1和BRCA2基因的突变会增加患乳腺癌的风险。我们确定了有或没有BRCA突变的患者的肿瘤病理特征和临床特征是否存在差异。
对1997年至2006年间接受BRCA突变基因检测的491例乳腺癌女性患者的肿瘤病理特征和临床特征进行了检查。对病历进行回顾性分析,以确定临床特征,包括种族、诊断时的年龄和临床分期、首次生育年龄、足月妊娠次数、口服避孕药和激素替代疗法的使用情况以及BRCA突变状态。对肿瘤病理进行复查,以确定组织学类型、肿瘤分级以及雌激素受体、孕激素受体和HER-2/neu状态。
在491例确诊为乳腺癌的患者中,391例患者BRCA阴性,86例患者BRCA阳性。三阴性乳腺癌(即雌激素受体、孕激素受体和HER-2/neu状态均为阴性的患者)在BRCA1阳性患者中占57.1%,在BRCA2阳性患者中占23.3%,在BRCA阴性患者中占13.8%。BRCA1突变携带者的肿瘤核分级高于其他两组(P <.001)。在三阴性乳腺癌患者中,BRCA2突变携带者诊断时的年龄比BRCA1突变携带者和非携带者更大(P <.01)。
这些结果表明,与BRCA1突变相关的肿瘤可能分为两个不同的组,即三阴性和非三阴性组。未来的研究应致力于确定BRCA1突变和三阴性乳腺癌患者是否比具有相似肿瘤病理的BRCA阴性患者对治疗反应更好。