Clinicopathological Characteristics and Clinical Outcome in Egyptian Female Breast Cancer Patients With and Without BRCA1/2 Mutations

S. Abdelhamid, H. El-mesallamy, Hm AbdelAziz, A. Zekri
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Abstract

Introduction: Germline mutations in BRCA1 and BRCA2 genes confer high risk of developing breast cancer. We sought to examine whether the clinicopathological characteristics and the clinical outcome differ in patients with and without BRCA mutations. Patients and Methods: A series of 103 Egyptian female patients were recruited from Breast Cancer Unit, Clinical Oncology Department, Ain Shams University, Egypt. The enrolled patients, unselected for age of onset or family history, were tested for BRCA1/2 mutations using HRM analysis and direct sequencing. The clinical and pathological features of the patients were retrospectively assessed and comparisons were made using Chi-square. Disease free survival (DFS) was estimated by Kaplan–Meier method and compared in the two groups with log-rank. Results: The overall rate of BRCA1/2 mutations was 44%. Novel deleterious mutations were detected and submitted to NCBI Clinvar database. Deleterious mutations were identified in 29 cases and unclassified variants in 32 cases, 15 of which had a co-occuring deleterious mutation. Patients with BRCA mutations tended to have early onset breast cancer compared to non-carriers (P=0.002), more often premenopausal (P=0.006), with a familial history of breast cancer as well as other cancers (P=0.005). BRCA-related breast cancers were more likely to have T3-T4 stage than wild type (41% versus 28%, P=0.02), positive lymph node involvement (78 versus 53%, P=0.007) and develop bilateral breast cancers (24% versus 9%, P =0.007). The incidence of ER negative and PR negative tumors was higher in BRCA carriers, but not statistically significant (P=0.17 and 0.15, respectively). No difference in HER-2/neu status was observed (P=0.25). Early age at onset, positive lymph node involvement, family history of any cancer were independent predictive factors for occurrence of BRCA1/2 mutations. The median follow-up time for the cohort was 5.53 years. Patients with BRCA mutations had poorer 5-year DFS compared to non-carriers (47.7% versus 67.4%, P=0.041); but Cox regression analysis failed to demonstrate a significant independent influence of BRCA mutation status on DFS. Conclusion: This study shows that BRCA-related breast cancers in the Egyptian population have distinctive clinical and tumor features as well as outcome. This data has important health implications for guiding cancer control policies.
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有或没有BRCA1/2突变的埃及女性乳腺癌患者的临床病理特征和临床结果
BRCA1和BRCA2基因的种系突变会增加患乳腺癌的风险。我们试图检查是否有和没有BRCA突变的患者的临床病理特征和临床结果不同。患者和方法:从埃及艾因沙姆斯大学临床肿瘤科乳腺癌科招募了103名埃及女性患者。未选择发病年龄或家族史的入组患者使用HRM分析和直接测序检测BRCA1/2突变。回顾性评价患者的临床和病理特征,并采用卡方法进行比较。用Kaplan-Meier法估计无病生存期(DFS),并用log-rank法比较两组患者的无病生存期。结果:BRCA1/2的总突变率为44%。检测到新的有害突变并提交到NCBI Clinvar数据库。29例发现有害突变,32例发现未分类变异,其中15例同时发生有害突变。与非携带者相比,BRCA突变患者倾向于早发性乳腺癌(P=0.002),绝经前(P=0.006)更常见,具有乳腺癌和其他癌症的家族史(P=0.005)。与野生型相比,brca相关乳腺癌更容易发生T3-T4期(41%对28%,P=0.02)、淋巴结阳性累及(78%对53%,P=0.007)和双侧乳腺癌(24%对9%,P=0.007)。BRCA携带者ER阴性和PR阴性肿瘤发生率较高,但差异无统计学意义(P分别为0.17和0.15)。HER-2/neu状态差异无统计学意义(P=0.25)。发病年龄早、淋巴结阳性累及、任何癌症家族史是发生BRCA1/2突变的独立预测因素。该队列的中位随访时间为5.53年。与非携带者相比,BRCA突变患者的5年DFS较差(47.7%对67.4%,P=0.041);但Cox回归分析未能证明BRCA突变状态对DFS有显著的独立影响。结论:本研究表明,埃及人群中brca相关乳腺癌具有独特的临床和肿瘤特征以及预后。这些数据对指导癌症控制政策具有重要的健康意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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