伊朗乳腺癌和卵巢癌患者BRCA1和BRCA2突变的模式和谱

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Shayan Forghani, Hamid Reza Mirzaee, Hamid Rezvani, Arman Forghani, Fatemeh Mahdavi Sabet, Ali Hojjat, Mona Malekzadeh, Atieh Akbari, Sanaz Tabarestani
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引用次数: 0

摘要

遗传BRCA1/2突变的女性患乳腺癌和卵巢癌的风险增加。关于这些突变的患病率和谱的报告主要集中在具有欧洲血统的个体上。此前一项针对伊朗乳腺癌患者的研究报道,早发性乳腺癌无BRCA1/2突变,无其他标准,这与其他人群相反。本研究的目的是表征伊朗乳腺癌和卵巢癌患者中这些突变的模式,并评估曼彻斯特评分系统对患者及其未受影响的家庭成员的预测效果。我们回顾性地回顾了对乳腺癌和卵巢癌患者以及具有阳性家族史的未受影响个体进行的基因检测。研究参与者是根据NCCN(国家综合癌症网络)标准(2.2024版)选择的。共有376名女性乳腺癌患者、49名卵巢癌患者和74名未受影响的个体参加了这项研究。在乳腺癌患者中,检测到24个(6.4%)BRCA1突变和23个(6.1%)BRCA2突变。在卵巢癌患者中,鉴定出9个(18.5%)BRCA1突变和1个(2%)BRCA2突变。在未受影响的个体中发现了三个(4.1%)BRCA2突变。7例癌症诊断年龄≤40岁且无其他标准(包括家族史)的乳腺癌患者存在潜在突变:4例BRCA2和3例BRCA1突变。曼彻斯特评分表现良好,灵敏度为81%,特异性为70%。需要更多的研究来阐明伊朗患者乳腺癌和卵巢癌的遗传成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The patterns and spectrum of BRCA1 and BRCA2 mutations in Iranian breast and ovarian cancer patients.

Women with inherited BRCA1/2 mutations are at increased risk of breast and ovarian cancer. The reports on the prevalence and spectrum of these mutations have been primarily focused on individuals with European ancestry. A previous study on Iranian breast cancer patients reported no BRCA1/2 mutation in early-onset breast cancer with no other criteria, which is contrary to other populations. The purpose of this study was to characterize the patterns of these mutations in Iranian breast and ovarian cancer patients and evaluate the predictive efficacy of the Manchester scoring system in patients and their unaffected family members. We retrospectively reviewed the genetic testing performed for breast and ovarian cancer patients and unaffected individuals with a positive family history. The study participants were selected based on the NCCN (National Comprehensive Cancer Network) criteria (version 2.2024). A total of 376 female breast cancer patients, 49 ovarian cancer patients, and 74 unaffected individuals were enrolled in this study. In breast cancer patients, 24 (6.4%) BRCA1 and 23 (6.1%) BRCA2 mutations were detected. In ovarian cancer patients, 9 (18.5%) BRCA1 and 1 (2%) BRCA2 mutations were identified. Three (4.1%) BRCA2 mutations were identified in unaffected individuals. Seven breast cancer patients with age of cancer diagnosis ≤ 40 and no other criteria (including family history) had an underlying mutation: Four BRCA2, and three BRCA1 mutations. The Manchester score performed well, with a sensitivity of 81% and a specificity of 70%. More research is needed to clarify the hereditary component of breast and ovarian cancer in Iranian patients.

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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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