首页> 外文期刊>Breast cancer research and treatment. >Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer.
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Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer.

机译:在基于人群的对侧乳腺癌风险研究中,BRCA1 / BRCA2突变携带者对乳腺癌的辅助性全身治疗。

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Given the greatly elevated risks of contralateral breast cancer (CBC) observed in breast cancer patients who carry mutations in BRCA1 and BRCA2, it is critical to determine the effectiveness of standard adjuvant therapies in preventing CBC in mutation carriers. The WECARE study is a matched, case-control study of 708 women with CBC as cases and 1,399 women with unilateral breast cancer (UBC) as controls, including 181 BRCA1/BRCA2 mutation carriers. Interviews and medical record reviews provided detailed information on risk factors and breast cancer therapy. All study participants were screened for BRCA1 and BRCA2 mutations using denaturing high-performance liquid chromatography (DHPLC) to detect genetic variants in the coding and flanking regions of the genes. Conditional logistic regression was used to compare the risk of CBC associated with chemotherapy and tamoxifen in BRCA1/BRCA2 mutation carriers and non-carriers. Chemotherapy was associated with lower CBC risk both in non-carriers (RR = 0.6 [95% CI: 0.5-0.7]) and carriers (RR = 0.5 [95% CI: 0.2-1.0]; P value = 0.04). Tamoxifen was associated with a reduced CBC risk in non-carriers (RR = 0.7 [95% CI: 0.6-1.0]; P value = 0.03). We observed a similar but non-significant reduction associated with tamoxifen in mutation carriers (RR = 0.7 [95% CI: 0.3-1.8]). The tests of heterogeneity comparing carriers to non-carriers did not provide evidence for a difference in the associations with chemotherapy (P value = 0.51) nor with tamoxifen (P value = 0.15). Overall, we did not observe a difference in the relative risk reduction associated with adjuvant treatment between BRCA1/BRCA2 mutation carriers and non-carriers. However, given the higher absolute CBC risk in mutation carriers, the potentially greater impact of adjuvant therapy in reducing CBC risk among mutation carriers should be considered when developing treatment plans for these patients.
机译:鉴于在携带BRCA1和BRCA2突变的乳腺癌患者中观察到对侧乳腺癌(CBC)的风险大大增加,因此确定标准辅助疗法在预防突变携带者中CBC的有效性中至关重要。 WECARE研究是一项匹配的病例对照研究,其中包括708名CBC妇女和1,399名单侧乳腺癌(UBC)妇女作为对照,包括181个BRCA1 / BRCA2突变携带者。访谈和病历审查提供了有关危险因素和乳腺癌治疗的详细信息。使用变性高效液相色谱(DHPLC)筛选所有受试者的BRCA1和BRCA2突变,以检测基因编码区和侧翼区的遗传变异。使用条件逻辑回归分析比较BRCA1 / BRCA2突变携带者和非携带者中与化疗和他莫昔芬相关的CBC风险。在非携带者(RR = 0.6 [95%CI:0.5-0.7])和携带者(RR = 0.5 [95%CI:0.2-1.0]; P值= 0.04)中,化疗与较低的CBC风险相关。他莫昔芬与非携带者的CBC风险降低相关(RR = 0.7 [95%CI:0.6-1.0]; P值= 0.03)。我们观察到与他莫昔芬在突变携带者中相关的相似但不显着的降低(RR = 0.7 [95%CI:0.3-1.8])。异质性测试将携带者与非携带者进行了比较,但没有提供证据表明化学疗法(P值= 0.51)和他莫昔芬(P值= 0.15)之间存在关联。总体而言,我们未观察到BRCA1 / BRCA2突变携带者和非携带者在与辅助治疗相关的相对风险降低方面存在差异。但是,鉴于突变携带者的绝对CBC风险较高,在制定针对这些患者的治疗计划时,应考虑辅助治疗对降低突变携带者的CBC风险的更大影响。

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