铂治疗生殖系BRCA1或BRCA2突变的早期乳腺癌患者的生存结局和疗效:一项多中心回顾性队列研究

IF 3.3 4区 医学 Q2 ONCOLOGY
Xi Chen, Xiaoyan Qian, Min Xiao, Pin Zhang
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引用次数: 0

摘要

目的:本研究旨在比较铂治疗BRCA1和BRCA2突变的早期乳腺癌患者的生存结局和疗效。方法:回顾性分析2016年4月至2021年1月在中国三家医疗机构诊断为I-III期乳腺癌并携带种系致病性/可能致病性BRCA突变的患者。收集所有符合条件的患者的临床和病理特征、治疗信息、BRCA的致病变异和生存结果的数据。结果:169例BRCA突变患者入组,包括BRCA1突变(53.3%,n = 90)和BRCA2突变(46.7%,n = 79)。中位年龄为39岁,大多数患者(68.1%,n = 115)为I-II期。BRCA1突变患者的组织学分级为III级(55.6%),Ki-67指数(Ki-67≥30%,78.9%)高于BRCA2突变患者(27.8%,58.2%)。BRCA1突变患者发生三阴性乳腺癌的比例明显高于BRCA2突变患者(71.1% vs 19.0%, P < 0.0001)。共有142例(84.0%)患者接受了新/辅助化疗,包括以蒽环素和/或紫杉烷为基础的方案(55.6%)或以铂为基础的方案(27.2%)。中位随访时间为33.2个月。BRCA1和BRCA2突变患者的3年无病生存期(DFS)和远期无复发生存期(DRFS)无显著差异(82.0% vs 85.4%, P = 0.35;94.3% vs 94.6%, P = 0.39)。铂治疗组BRCA1突变队列患者3年DFS率显著高于非铂治疗组(96.0% vs 75.2%, P = 0.01)。BRCA2突变患者接受铂治疗方案和非铂治疗方案的DFS和DRFS无差异。结论:BRCA1和BRCA2突变的早期乳腺癌患者生存结局相似,但生物学特性不同。BRCA1突变患者从铂方案中获益更多。铂方案对BRCA1和BRCA2早期乳腺癌患者的价值有待进一步验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Survival Outcomes and Efficacy of Platinum in Early Breast Cancer Patients with Germline BRCA1 or BRCA2 Mutation: A Multicenter Retrospective Cohort Study.

Survival Outcomes and Efficacy of Platinum in Early Breast Cancer Patients with Germline BRCA1 or BRCA2 Mutation: A Multicenter Retrospective Cohort Study.

Survival Outcomes and Efficacy of Platinum in Early Breast Cancer Patients with Germline BRCA1 or BRCA2 Mutation: A Multicenter Retrospective Cohort Study.

Survival Outcomes and Efficacy of Platinum in Early Breast Cancer Patients with Germline BRCA1 or BRCA2 Mutation: A Multicenter Retrospective Cohort Study.

Purpose: The study aimed to compare the survival outcomes and efficacy of platinum in early breast cancer patients with BRCA1 and BRCA2 mutations.

Methods: Patients diagnosed with stage I-III breast cancer and carrying germline pathogenic/likely pathogenic BRCA mutations in three medical institutions in China from April 2016 to January 2021 were retrospectively analyzed. Data on clinical and pathological characteristics, treatment information, pathogenic variants of BRCA, and survival outcomes were collected for all eligible patients.

Outcomes: One hundred and sixty-nine patients with BRCA mutations were enrolled, including BRCA1 mutation (53.3%, n = 90) and BRCA2 mutation (46.7%, n = 79). The median age was 39 years, and most patients (68.1%, n = 115) were stage I-II. Patients with BRCA1 mutations were characterized by histological grade III (55.6%) and higher Ki-67 index (Ki-67 ≥ 30%, 78.9%) compared with patients with BRCA2 mutations (27.8%, 58.2%). BRCA1 mutation patients accounted for a significantly higher proportion of triple negative breast cancer than BRCA2 mutation patients (71.1% vs 19.0%, P < 0.0001). A total of 142 (84.0%) patients received neo/adjuvant chemotherapy, including anthracycline and/or taxane-based regimens (55.6%) or platinum-based regimens (27.2%). Median follow-up was 33.2 months. Three-year DFS (disease-free survival) and DRFS (distant recurrence-free survival) had no significant differences between patients with BRCA1 and BRCA2 mutations (82.0% vs 85.4%, P = 0.35; 94.3% vs 94.6%, P = 0.39). The 3-year DFS rate in BRCA1 mutation cohort of patients received platinum regimen was significantly higher than patients received non-platinum regimen (96.0% vs 75.2%, P = 0.01). No differences between DFS and DRFS were observed in patients with BRCA2 mutation received platinum regimen and non-platinum regimen.

Conclusion: Similar survival outcomes were observed in early breast cancer patients with BRCA1 and BRCA2 mutation, though they had different biological characteristics. Patients with BRCA1 mutations are more benefit from platinum-regimen. The value of platinum-regimen for early breast cancer patients with BRCA1 and BRCA2 needs to be verified further.

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