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CDH1 基因突变携带者行全胃切除术的适应证及微创和开放胃癌根治术的风险降低效果。

Indications for Total Gastrectomy in CDH1 Mutation Carriers and Outcomes of Risk-Reducing Minimally Invasive and Open Gastrectomies.

机构信息

Gastric and Mixed Tumor Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York.

Clinical Genetics Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

JAMA Surg. 2020 Nov 1;155(11):1050-1057. doi: 10.1001/jamasurg.2020.3356.

Abstract

IMPORTANCE

CDH1 variants are increasingly identified on commercially available multigene panel tests, calling for data to inform counseling of individuals without a family history of gastric cancer.

OBJECTIVES

To assess association between CDH1 variant pathogenicity or family history of gastric or lobular breast cancer and identification of signet ring cell cancer and to describe outcomes of risk-reducing minimally invasive and open total gastrectomy.

DESIGN, SETTING, AND PARTICIPANTS: This cohort study was performed from January 1, 2006, to January 1, 2020, in 181 patients with CDH1 germline variants from a single institution.

INTERVENTIONS

Genetic counseling, esophagogastroduodenoscopy, and possible total gastrectomy.

MAIN OUTCOMES AND MEASURES

CDH1 variant classification, family cancer history, findings of signet ring cell carcinoma at esophagogastroduodenoscopy and surgery, postoperative events and weight changes, and follow-up.

RESULTS

Of 181 individuals with CDH1 germline variants (mean [SD] age at time of testing, 44 [15] years; 126 [70%] female), 165 harbored a pathogenic or likely pathogenic variant. Of these patients, 101 underwent open (n = 58) or minimally invasive (n = 43) total gastrectomy. Anastomotic leaks that required drainage were infrequent (n = 3), and median long-term weight loss was 20% (interquartile range [IQR], 10%-23%). In those undergoing minimally invasive operations, more lymph nodes were retrieved (median, 28 [IQR, 20-34] vs 15 [IQR, 9-19]; P < .001) and the hospital stay was 1 day shorter (median, 6 [IQR, 5-7] vs 7 [IQR, 6-7] days; P = .04). Signet ring cell cancer was identified in the surgical specimens of 85 of 95 patients (89%) with a family history of gastric cancer and 4 of 6 patients (67%) who lacked a family history. Among the latter 6 patients, 4 had a personal or family history of lobular breast cancer, including 2 with signet ring cell cancer. Of the 16 patients with pathogenic or likely pathogenic CDH1 variants who presented with locally advanced or metastatic gastric cancer, 3 (19%) had no family history of gastric cancer or personal or family history of lobular breast cancer.

CONCLUSIONS AND RELEVANCE

Total gastrectomy may be warranted for patients with pathogenic or likely pathogenic CDH1 variants and a family history of gastric or lobular breast cancer and may be appropriate for those without a family history. A minimally invasive approach is feasible and may be preferred for selected patients.

摘要

重要性

越来越多的 CDH1 变体在商业上可获得的多基因面板测试中被发现,这就需要数据来为没有胃癌家族史的个体提供咨询。

目的

评估 CDH1 变体的致病性或胃癌和乳腺癌家族史与识别印戒细胞癌之间的关联,并描述减少风险的微创和开放性全胃切除术的结果。

设计、地点和参与者:这项队列研究于 2006 年 1 月 1 日至 2020 年 1 月 1 日在一个机构的 181 名 CDH1 种系变异患者中进行。

干预措施

遗传咨询、食管胃十二指肠镜检查和可能的全胃切除术。

主要结果和措施

CDH1 变体分类、家族癌症史、食管胃十二指肠镜和手术中发现的印戒细胞癌、术后事件和体重变化以及随访。

结果

在 181 名携带 CDH1 种系变异的个体中(检测时的平均[标准差]年龄,44[15]岁;126[70%]为女性),165 名携带致病性或可能致病性变异。这些患者中有 101 人接受了开放性(n=58)或微创性(n=43)全胃切除术。需要引流的吻合口漏很少见(n=3),长期体重中位数下降 20%(四分位距[IQR],10%-23%)。在接受微创手术的患者中,更多的淋巴结被切除(中位数,28[IQR,20-34] vs 15[IQR,9-19];P<.001),住院时间缩短 1 天(中位数,6[IQR,5-7] vs 7[IQR,6-7]天;P=.04)。在有胃癌家族史的 95 名患者中的 85 名(89%)和无家族史的 6 名患者中的 4 名(67%)的手术标本中发现了印戒细胞癌。在后者 6 名患者中,4 名有个人或家族史的乳腺癌,包括 2 名有印戒细胞癌。在 16 名携带致病性或可能致病性 CDH1 变异且患有局部晚期或转移性胃癌的患者中,有 3 名(19%)没有胃癌家族史或个人或家族史的乳腺癌。

结论和相关性

对于携带致病性或可能致病性 CDH1 变体且有胃癌或乳腺癌家族史的患者,全胃切除术可能是必要的,对于没有家族史的患者,也可能是合适的。微创方法是可行的,可能更适合某些患者。

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