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个性化医疗时代遗传性乳腺癌易感性检测的考量因素

Considerations in Testing for Inherited Breast Cancer Predisposition in the Era of Personalized Medicine.

作者信息

Powers Benjamin, Pal Tuya, Laronga Christine

机构信息

Department of Breast Oncology, H. Lee Moffitt Cancer Center, 10920 N. Mckinley Drive, Tampa, FL 33612, USA.

Department of Medicine, Vanderbilt University Medical Center, Vanderbilt-Ingram Cancer Center, Nashville, TN, USA.

出版信息

Surg Oncol Clin N Am. 2018 Jan;27(1):1-22. doi: 10.1016/j.soc.2017.08.003.

Abstract

Technological advances realized through next-generation sequencing technologies coupled with the loss of the ability to patent genes have led to reduction in costs for genetic testing. As a result, more people are being identified with inherited breast cancer syndromes that may affect recommendations for surveillance and risk reduction. Surgeons, at the forefront for patients newly diagnosed with breast cancer, must keep current with the changing landscape of genetics to continue to provide appropriate counsel and care. This article provides an overview of individuals at risk for inherited cancer predisposition and recommendations for surveillance and management.

摘要

通过下一代测序技术实现的技术进步,再加上基因专利能力的丧失,导致基因检测成本降低。因此,越来越多的人被诊断出患有遗传性乳腺癌综合征,这可能会影响监测和降低风险的建议。作为新诊断乳腺癌患者的前沿人员,外科医生必须跟上遗传学不断变化的形势,以便继续提供适当的咨询和护理。本文概述了有遗传性癌症易感性风险的个体以及监测和管理的建议。

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