Liquid Biopsies for the Personalized Management of Patients With Hereditary Diffuse Gastric Cancer (LISA-HDGC)
Primary Purpose
Hereditary Diffuse Gastric Cancer
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Liquid biopsies (blood, gastric fluid).
Sponsored by
About this trial
This is an interventional diagnostic trial for Hereditary Diffuse Gastric Cancer
Eligibility 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 > 18years old
- Patients with no oncological history
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
Sites / Locations
- Hopital Pitié SalpetrièreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Unaffected carriers of constitutional mutations
All patients with FOGD
Arm Description
Patients with CDH1 or CTNNA1 germline pathogenic variant. No history of diffuse gastric cancer.
without observation of macroscopic lesions paired with cases (age and sex)
Outcomes
Primary Outcome Measures
Number of subjects in whom somatic mutations or methylation profiles are detected.
Secondary Outcome Measures
Replicability of observations over successive endoscopies. Correlation between blood and gastric fluid.
Full Information
NCT ID
NCT04253106
First Posted
January 31, 2020
Last Updated
October 31, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT04253106
Brief Title
Liquid Biopsies for the Personalized Management of Patients With Hereditary Diffuse Gastric Cancer
Acronym
LISA-HDGC
Official Title
Liquid Biopsies (Blood, Gastric Fluid) for the Personalized Management of Patients With Hereditary Diffuse Gastric Cancer: a Pilot Project
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 26, 2020 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
February 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
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.
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hereditary Diffuse Gastric Cancer
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Multicentric, prospective non-randomized study prognostic aim. Control group planned to have standard values.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Unaffected carriers of constitutional mutations
Arm Type
Experimental
Arm Description
Patients with CDH1 or CTNNA1 germline pathogenic variant. No history of diffuse gastric cancer.
Arm Title
All patients with FOGD
Arm Type
Active Comparator
Arm Description
without observation of macroscopic lesions paired with cases (age and sex)
Intervention Type
Genetic
Intervention Name(s)
Liquid biopsies (blood, gastric fluid).
Intervention Description
Next generation sequencing of a panel of diffuse gastric cancer genes, methylation analysis. Samples collected during routine screening endoscopy.
Primary Outcome Measure Information:
Title
Number of subjects in whom somatic mutations or methylation profiles are detected.
Time Frame
Over two years of surveillance
Secondary Outcome Measure Information:
Title
Replicability of observations over successive endoscopies. Correlation between blood and gastric fluid.
Time Frame
Over two years of surveillance
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility 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 > 18years old
Patients with no oncological history
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
BENUSIGLIO Patrick, MD PhD
Phone
33142177659
Email
patrick.benusiglio@aphp.fr
Facility Information:
Facility Name
Hopital Pitié Salpetrière
City
Paris
ZIP/Postal Code
75013
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrick Benusiglio, MD, PhD
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data entry and management under the responsibility of Dr Patrick Benusiglio investigator coordinating the study
Learn more about this trial
Liquid Biopsies for the Personalized Management of Patients With Hereditary Diffuse Gastric Cancer
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