医学
癌症
乳腺癌
基因检测
预防性手术
癌症综合征
CDH1
林奇综合征
人口
内科学
肿瘤科
突变
外科
种系突变
结直肠癌
遗传学
DNA错配修复
基因
细胞
钙粘蛋白
环境卫生
生物
作者
Lauren A. Gamble,Theo Heller,Jeremy L. Davis
出处
期刊:JAMA Surgery
[American Medical Association]
日期:2021-04-01
卷期号:156 (4): 387-387
被引量:40
标识
DOI:10.1001/jamasurg.2020.6155
摘要
Inherited variants in the tumor suppressor gene CDH1 are associated with an increased risk of gastric and breast cancers. This review aims to address the most current topics in management of the hereditary diffuse gastric cancer syndrome attributed to CDH1.Consensus management guidelines have broadened genetic testing criteria for CDH1. Prophylactic total gastrectomy is recommended for any pathogenic or likely pathogenic CDH1 variant carrier starting at the age of 20 years. Annual surveillance endoscopy is recommended to those who defer prophylactic total gastrectomy. Women with a CDH1 variant should initiate magnetic resonance imaging breast surveillance starting at age 30 years. Further research is needed to understand the pathogenesis of early-stage gastric cancers (T1a), which are pathognomonic of hereditary diffuse gastric cancer syndrome, that lead to advanced gastric cancer to develop both treatment and prevention strategies for this patient population.The heritable CDH1 gene mutation is of importance to today's surgeons because it is associated with a substantial increased risk of developing both gastric and breast cancers. Management of this cancer syndrome currently uses prophylactic surgery and enhanced cancer surveillance strategies.
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