Cisco Robin M, Norton Jeffrey A
Stanford University School of Medicine, Department of Surgery, Stanford, CA 94305, USA.
Future Oncol. 2008 Aug;4(4):553-9. doi: 10.2217/14796694.4.4.553.
Hereditary diffuse gastric cancer (HDGC) is an inherited cancer-susceptibility syndrome characterized by autosomal dominance and high penetrance. In 30-50% of cases, a causative germline mutation in CDH1, the E-cadherin gene, may be identified. Female carriers of CDH1 mutations also have an increased (20-40%) risk of lobular breast cancer. Endoscopic surveillance of patients with CDH1 mutations is ineffective because early foci of HDGC are typically small and underlie normal mucosa. CDH1 mutation carriers are therefore offered the option of prophylactic gastrectomy, which commonly reveals early foci of invasive signet-ring cell cancer. We review recommendations for genetic testing, surveillance and prophylactic surgery in HDGC. Areas for future research are discussed, including development of new screening modalities, optimal timing of prophylactic gastrectomy, identification of additional causative mutations in HDGC, management of patients with CDH1 missense mutations and prevention/early detection of lobular breast cancer in CDH1 mutation carriers.
遗传性弥漫性胃癌(HDGC)是一种遗传性癌症易感性综合征,其特征为常染色体显性遗传和高外显率。在30%至50%的病例中,可能会发现E-钙黏蛋白基因(CDH1)的致病性种系突变。CDH1突变的女性携带者患小叶乳腺癌的风险也会增加(20%至40%)。对CDH1突变患者进行内镜监测无效,因为HDGC的早期病灶通常较小,位于正常黏膜之下。因此,CDH1突变携带者可选择预防性胃切除术,该手术通常能发现浸润性印戒细胞癌的早期病灶。我们回顾了HDGC基因检测、监测和预防性手术的相关建议。讨论了未来的研究方向,包括新筛查方式的开发、预防性胃切除术的最佳时机、HDGC其他致病性突变的鉴定、CDH1错义突变患者的管理以及CDH1突变携带者小叶乳腺癌的预防/早期检测。