Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Mail Stop M4-B874, Seattle, WA 98109-1024, USA.
Breast Cancer Res Treat. 2010 Sep;123(2):491-8. doi: 10.1007/s10549-010-0769-3. Epub 2010 Feb 5.
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.
鉴于携带 BRCA1 和 BRCA2 基因突变的乳腺癌患者发生对侧乳腺癌(CBC)的风险大大增加,因此确定标准辅助治疗在预防突变携带者中 CBC 的有效性至关重要。WECARE 研究是一项针对 708 例 CBC 患者(病例)和 1399 例单侧乳腺癌(UBC)患者(对照)的配对病例对照研究,其中包括 181 例 BRCA1/BRCA2 基因突变携带者。访谈和病历回顾提供了有关危险因素和乳腺癌治疗的详细信息。所有研究参与者均使用变性高效液相色谱法(DHPLC)进行 BRCA1 和 BRCA2 基因突变筛查,以检测基因编码和侧翼区域的遗传变异。条件逻辑回归用于比较 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)。我们观察到突变携带者中与他莫昔芬相关的类似但无统计学意义的降低(RR=0.7[95%CI:0.3-1.8])。比较携带者与非携带者的异质性检验未提供化疗(P 值=0.51)或他莫昔芬(P 值=0.15)关联差异的证据。总体而言,我们没有观察到 BRCA1/BRCA2 突变携带者与非携带者之间与辅助治疗相关的相对风险降低存在差异。然而,鉴于突变携带者中 CBC 的绝对风险较高,在制定这些患者的治疗计划时,应考虑辅助治疗降低 CBC 风险的潜在更大影响。