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临床试验/NCT04253106
NCT04253106已完成不适用

Liquid Biopsies (blood, Gastric Fluid) for the Personalized Management of Patients with Hereditary Diffuse Gastric Cancer: a Pilot Project

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2020年11月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
1
主要终点
Number of subjects in whom somatic mutations or methylation profiles are detected.

研究概览

简要总结

Activating somatic mutations and methylation profiles identified by liquid biopsies could identify CDH1 and CTNNA1 pathogenic variants carriers with invasive diffuse gastric cancer undetectable by upper G-I endoscopy.

详细描述

Carriers of germline pathogenic variants in the CDH1 and CTNNA1 genes have the Hereditary Diffuse Gastric Cancer Syndrome. Asymptomatic carriers have at high lifetime risk of diffuse gastric cancer (30-70%). Screening upper gastrointestinal endoscopy, even with multiple random biopsies, misses signet ring cell cancer foci. Invasive cancers can thus go undetected. There is therefore a recommendation of total risk-reducing gastrectomy, at least in carriers with a family history of gastric cancer. Novel screening strategies are needed. In this pilot project, the investigators will perform liquid biopsies of both blood and gastric fluid in asymptomatic carriers who refuse gastrectomy and in controls. The investigators aim to show that somatic mutations in a panel of genes involved in gastric cancer and methylation profiles are detected in a subset of carriers, and not in controls. These could be indicative of invasive cancer undetected by endoscopy, and would thus be a strong argument for risk-reducing gastrectomy. On the contrary, in the absence of somatic mutations in liquid biopsies, endoscopic surveillance could continue.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patient ≥ 18 years old
  • •CDH1 or CTNNA1 germline pathogenic variant.
  • •No history of diffuse gastric cancer.
  • •French social security.
  • •Ability to understand and willingness to sign a written informed consent document.
  • •Volunteers:
  • •Patients ≥ 18 years old
  • •Patients with no oncological history
  • •Patients with macroscopically normal oeso-gastroduodenal fibroscopy
  • •French social security.
  • •Ability to understand and willingness to sign a written informed consent

排除标准

  • •for both arms
  • •Patients with cancer being treated
  • •Patients with metastatic cancer
  • •Medical contraindication to general anesthesia or FOGD (bleeding disorder, pregnant women )
  • •Patients under guardianship or curator

研究组 & 干预措施

Unaffected carriers of constitutional mutations

Experimental

Patients with CDH1 or CTNNA1 germline pathogenic variant. No history of diffuse gastric cancer.

干预措施: Liquid biopsies (blood, gastric fluid). (Genetic)

All patients with FOGD

Active Comparator

without observation of macroscopic lesions paired with cases (age and sex)

干预措施: Liquid biopsies (blood, gastric fluid). (Genetic)

结局指标

主要结局

Number of subjects in whom somatic mutations or methylation profiles are detected.

时间窗: Over two years of surveillance

次要结局

  • Replicability of observations over successive endoscopies. Correlation between blood and gastric fluid.(Over two years of surveillance)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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