乳腺癌与 ATM 基因突变:治疗意义。

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2024-11-14 DOI:10.1186/s13053-024-00300-9
Marta Seca, Steven A Narod
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引用次数: 0

摘要

乳腺癌易感基因的基因检测已超出 BRCA1 和 BRCA2 的范围,现在包括 20 个或更多基因的检测。现在建议所有 65 岁或 65 岁以下确诊为乳腺癌的妇女接受扩展基因组检测。检测的理由包括根据发现的基因突变对乳腺癌进行个性化治疗。对于 BRCA1 和 BRCA2 基因携带者来说,突变的发现对癌症的治疗有明确的影响,但对于其他基因,如 ATM 基因,其治疗影响就不那么明确了。有 ATM 基因突变的女性一生中患乳腺癌的风险约为 25%,其中大部分为 ER 阳性。罹患卵巢癌的风险约为 5%。目前还不清楚在新诊断的乳腺癌患者中发现 ATM 基因突变会对其治疗和随访产生什么影响。目前,对这些妇女的治疗方法与未发现突变的妇女相同。重要的是,应开展大型前瞻性研究,对乳腺癌和 ATM 基因突变女性患者的各种治疗方式进行研究,以优化治疗效果。
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Breast cancer and ATM mutations: treatment implications.

Genetic testing for breast cancer predisposing genes has expanded beyond BRCA1 and BRCA2 and now includes panels of 20 or more genes. It is now recommended that all women diagnosed with breast cancer at age 65 or below be offered testing for an extended gene panel. The rationale for testing includes personalizing the management of breast cancer according to the mutation found. For BRCA1 and BRCA2 carriers, the finding of a mutation has clear implications for cancer management, but for other genes, such as ATM, the management implications are less clear. Women with an ATM mutation have a lifetime risk of breast cancer of approximately 25%, the majority of which are ER-positive. The risk of ovarian cancer is approximately 5%. It is not yet clear how the identification of an ATM mutation in a patient newly diagnosed with breast cancer should impact on her treatment and follow-up. At present, these women are treated in the same way as women without a mutation. It is important that large prospective studies be conducted looking at various treatment modalities in women with breast cancer and an ATM mutation in order to optimize outcomes.

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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
期刊最新文献
BRCA2 germline mutation carrier with five malignancies: a case report. A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives. Breast cancer and ATM mutations: treatment implications. Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2023". Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing.
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