Suppr超能文献

遗传/家族性高风险评估:乳腺和卵巢,第 2.2015 版。

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.

机构信息

Fox Chase Cancer Center

The Ohio State University Comprehensive Cancer Center - James Cancer Hospital and Solove Research Institute

出版信息

J Natl Compr Canc Netw. 2016 Feb;14(2):153-62. doi: 10.6004/jnccn.2016.0018.

Abstract

The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast and Ovarian provide recommendations for genetic testing and counseling and risk assessment and management for hereditary cancer syndromes. Guidelines focus on syndromes associated with an increased risk of breast and/or ovarian cancer and are intended to assist with clinical and shared decision-making. These NCCN Guidelines Insights summarize major discussion points of the 2015 NCCN Genetic/Familial High-Risk Assessment: Breast and Ovarian panel meeting. Major discussion topics this year included multigene testing, risk management recommendations for less common genetic mutations, and salpingectomy for ovarian cancer risk reduction. The panel also discussed revisions to genetic testing criteria that take into account ovarian cancer histology and personal history of pancreatic cancer.

摘要

美国国家综合癌症网络(NCCN)《遗传/家族性高风险评估:乳腺和卵巢》指南提供了遗传性癌症综合征的基因检测和咨询、风险评估以及管理建议。指南重点关注与乳腺癌和/或卵巢癌风险增加相关的综合征,并旨在协助临床和共同决策。这些 NCCN 指南解读总结了 2015 年 NCCN 遗传/家族性高风险评估:乳腺和卵巢专家组会议的主要讨论要点。今年的主要讨论话题包括多基因检测、罕见基因突变的风险管理建议,以及预防性输卵管切除术降低卵巢癌风险。专家组还讨论了遗传检测标准的修订,这些修订考虑了卵巢癌的组织学和个人胰腺癌病史。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验