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Liquid Biopsies for the Personalized Management of Patients with Hereditary Diffuse Gastric Cancer (LISA-HDGC)

A

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Hereditary Diffuse Gastric Cancer

Treatments

Genetic: Liquid biopsies (blood, gastric fluid).

Study type

Interventional

Funder types

Other

Identifiers

NCT04253106
APHP190483

Details and patient eligibility

About

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.

Full description

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.

Enrollment

16 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Case:

  • 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

Exclusion Criteria: 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

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

16 participants in 2 patient groups

Unaffected carriers of constitutional mutations
Experimental group
Description:
Patients with CDH1 or CTNNA1 germline pathogenic variant. No history of diffuse gastric cancer.
Treatment:
Genetic: Liquid biopsies (blood, gastric fluid).
All patients with FOGD
Active Comparator group
Description:
without observation of macroscopic lesions paired with cases (age and sex)
Treatment:
Genetic: Liquid biopsies (blood, gastric fluid).

Trial contacts and locations

1

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Central trial contact

BENUSIGLIO Patrick, MD PhD

Data sourced from clinicaltrials.gov

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