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本文引用的文献

1
Response to neoadjuvant systemic therapy for breast cancer in BRCA mutation carriers and noncarriers: a single-institution experience.BRCA 基因突变携带者和非携带者乳腺癌新辅助全身治疗的反应:单中心经验。
J Clin Oncol. 2011 Oct 1;29(28):3739-46. doi: 10.1200/JCO.2011.35.2682. Epub 2011 Sep 6.
2
Clinical outcome of triple negative breast cancer in BRCA1 mutation carriers and noncarriers.BRCA1 突变携带者与非携带者三阴性乳腺癌的临床结局。
Cancer. 2011 Jul 15;117(14):3093-100. doi: 10.1002/cncr.25911. Epub 2011 Jan 24.
3
Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer.三阴性乳腺癌中未选择患者的 BRCA 突变发生率和结局。
Clin Cancer Res. 2011 Mar 1;17(5):1082-9. doi: 10.1158/1078-0432.CCR-10-2560. Epub 2011 Jan 13.
4
A positive feedback loop of ER-α36/EGFR promotes malignant growth of ER-negative breast cancer cells.雌激素受体-α36/表皮生长因子受体正反馈环路促进雌激素受体阴性乳腺癌细胞的恶性生长。
Oncogene. 2011 Feb 17;30(7):770-80. doi: 10.1038/onc.2010.458. Epub 2010 Oct 11.
5
Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.BRCA1 或 BRCA2 基因突变携带者的降低风险手术与癌症风险和死亡率的关联。
JAMA. 2010 Sep 1;304(9):967-75. doi: 10.1001/jama.2010.1237.
6
Expanding the criteria for BRCA mutation testing in breast cancer survivors.扩大乳腺癌幸存者中 BRCA 基因突变检测的标准。
J Clin Oncol. 2010 Sep 20;28(27):4214-20. doi: 10.1200/JCO.2010.28.0719. Epub 2010 Aug 23.
7
Classical cyclophosphamide, methotrexate, and fluorouracil chemotherapy is more effective in triple-negative, node-negative breast cancer: results from two randomized trials of adjuvant chemoendocrine therapy for node-negative breast cancer.经典环磷酰胺、甲氨蝶呤和氟尿嘧啶化疗在三阴性、淋巴结阴性乳腺癌中更有效:来自淋巴结阴性乳腺癌辅助化放疗的两项随机试验的结果。
J Clin Oncol. 2010 Jun 20;28(18):2966-73. doi: 10.1200/JCO.2009.25.9549. Epub 2010 May 10.
8
Effect of BRCA1/2 mutation on short-term and long-term breast cancer survival: a systematic review and meta-analysis.BRCA1/2 基因突变对短期和长期乳腺癌生存的影响:系统评价和荟萃分析。
Breast Cancer Res Treat. 2010 Jul;122(1):11-25. doi: 10.1007/s10549-010-0859-2. Epub 2010 Apr 8.
9
Favourable ten-year overall survival in a Caucasian population with high probability of hereditary breast cancer.在白种人群体中,高遗传性乳腺癌概率下十年整体存活率良好。
BMC Cancer. 2010 Mar 10;10:90. doi: 10.1186/1471-2407-10-90.
10
Prognosis of BRCA-associated breast cancer: a summary of evidence.BRCA 相关性乳腺癌的预后:证据总结。
Breast Cancer Res Treat. 2010 Jan;119(1):13-24. doi: 10.1007/s10549-009-0566-z.

三阴性乳腺癌患者中存在或不存在有害 BRCA 突变的患者的结局。

Outcome of triple-negative breast cancer in patients with or without deleterious BRCA mutations.

机构信息

Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Breast Cancer Res Treat. 2011 Nov;130(1):145-53. doi: 10.1007/s10549-011-1711-z. Epub 2011 Aug 10.

DOI:10.1007/s10549-011-1711-z
PMID:21830012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4334122/
Abstract

More than 75% of breast cancers that develop in BRCA1 mutation carriers are triple-negative breast cancers (TNBC). The aim of this study was to compare the recurrence-free survival (RFS) and overall survival (OS) in high-risk patients with TNBC with and without deleterious BRCA1/2 mutations. A total of 227 women with TNBC who were referred for genetic counseling and underwent BRCA genetic testing between 1997 and 2010 were included in the study. The relationships between clinical variables and outcomes were evaluated using univariate and multivariate Cox proportional hazard regression models. Of 227 high-risk women with TNBC, 50% (n = 114) tested positive for BRCA1/2 mutations. Age, race, and tumor characteristics did not differ between BRCA non-carriers and carriers. At a median follow-up of 3.4 years, the 5-year RFS rates were 74 and 81% (P = 0.21), and 5-year OS rates were 85 and 93% in BRCA non-carriers and BRCA carriers, respectively (P = 0.11). In a multivariate model, after adjusting for age and disease stage, BRCA carriers tended to have a decreased risk of recurrence (HR = 0.67; 95% CI: 0.38-1.19; P = 0.17) or death (HR = 0.51; 95% CI:0.23-1.17; P = 0.11) compared to non-carriers. Our data indicate a 50% prevalence of deleterious BRCA1/2 mutations in high-risk women diagnosed with TNBC. Overall prognosis of TNBC in BRCA carriers and non-carriers is not significantly different within the first 5 years following an initial diagnosis. Further studies need to evaluate whether different therapies will change the outcome in these subgroups of TNBC.

摘要

超过 75%的 BRCA1 基因突变携带者中发生的乳腺癌为三阴性乳腺癌(TNBC)。本研究旨在比较 BRCA1/2 有害突变阳性和阴性的高危 TNBC 患者的无复发生存率(RFS)和总生存率(OS)。本研究共纳入了 227 例于 1997 年至 2010 年间因遗传咨询并接受 BRCA 基因检测的 TNBC 高危患者。采用单因素和多因素 Cox 比例风险回归模型评估临床变量与结局的关系。在 227 例高危 TNBC 患者中,50%(n=114)BRCA1/2 突变阳性。BRCA 非携带者和携带者的年龄、种族和肿瘤特征无差异。中位随访 3.4 年后,BRCA 非携带者和携带者的 5 年 RFS 率分别为 74%和 81%(P=0.21),5 年 OS 率分别为 85%和 93%(P=0.11)。多因素模型调整年龄和疾病分期后,BRCA 携带者的复发风险(HR=0.67;95%CI:0.38-1.19;P=0.17)或死亡风险(HR=0.51;95%CI:0.23-1.17;P=0.11)均有降低趋势。本研究数据表明,高危 TNBC 患者中 BRCA1/2 有害突变的发生率为 50%。BRCA 携带者和非携带者在初始诊断后 5 年内总体预后无显著差异。进一步的研究需要评估不同的治疗方法是否会改变这些 TNBC 亚组的结局。