首页> 美国卫生研究院文献>Cancers >Contralateral Prophylactic Mastectomy in Women with Unilateral Breast Cancer Who Are Genetic Carriers Have a Strong Family History or Are just Young at Presentation
【2h】

Contralateral Prophylactic Mastectomy in Women with Unilateral Breast Cancer Who Are Genetic Carriers Have a Strong Family History or Are just Young at Presentation

机译:是遗传载体的单侧乳腺癌妇女的对侧预防性乳房切除术拥有强大的家庭历史或者在演示时只年轻

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The uptake of contralateral prophylactic mastectomy is rising with increasing trends that are possibly highest in the USA. Whilst its role is generally accepted in carriers of recognized high-risk predisposition genes such as BRCA1 and BRCA2 when the affected individual is premenopausal, controversy surrounds the benefit in less understood risk-profile clinical scenarios. This comprehensive review explores the current evidence underpinning the role of contralateral prophylactic mastectomy and its impact on contralateral breast cancer risk and survival in three distinct at-risk groups affected by unilateral breast cancer: known genetic carriers, those with strong familial risk but no demonstrable genetic mutation and women who are of young age at presentation. The review supports the role of contralateral prophylactic mastectomy in “high risk” groups where the evidence suggests a reduction in contralateral breast cancer risk. However, this benefit is less evident in women who are just young at presentation or those who have strong family history but no demonstrable genetic mutation. A multidisciplinary and personalized approach to support individuals in a shared-decision making process is recommended.
机译:对侧预防性乳房切除术的摄取与增加是可能在美国最高的呈上升趋势。虽然它的作用是公认的高风险易感基因如BRCA1和BRCA2的运营商普遍接受时,受影响的个体是绝经前,争议围绕在这些认识不足的风险轮廓临床方案的好处。该全面检讨探讨了目前的证据托换对侧预防性乳房切除术,并在受单侧乳腺癌三个不同的高危人群及其对对侧乳腺癌的风险和生存影响的作用:已知的基因携带者,那些具有很强的家族性风险,但没有证明的遗传突变和女性谁在演讲年轻的年龄。审查支持对侧预防性乳房切除术的“高危”人群,其中有证据表明在对侧乳腺癌风险降低的作用。然而,这样的好处是在妇女谁是在演示或只是年轻那些谁拥有强大的家族病史,但没有证明的基因突变不太明显。建议多学科和个性化的方式在共享的决策过程的支持人员。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号