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RECRUITINGINTERVENTIONAL

Circulating Biomarker Signatures for the Detection of Gastric Preneoplasia and Cancer

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The goal of this study is to characterize and validate a signature of circulating biomarkers in plasma, associated with the presence of gastric preneoplasia in patients with preexisting gastric lesion compared with a control group. For this purpose: * Patients with pre-existing gastric lesions will be invited to participate to this study. If they are willing to participate an additional blood sample (9 mL) will be collected at the time of the blood collection performed during their routine care * Healthy subjects will be invited to participate to constitute the control group. If they are willing to participate a blood sample (9 ml) will be drawn specifically for this study

Who May Be Eligible (Plain English)

Who May Qualify: Common - 18 years old or highter - written willing to sign a consent form prior to any study procedure - Affiliated to a social insurance system Specific to patients with gastric lesions - Untreated glandular atrophy (with or without intestinal metaplasia and/or dysplasia) and histologically diagnosed as of 2014 - Treatment naïve Gastric cancer (distal or proximal adenocarcinoma) Who Should NOT Join This Trial: Common - autoimmune conditions (where your immune system attacks your own body) or disease that impacts the immune system (e.g: HIV) - Chronic inflammatory disease - Known evolutive cancer (excluding gastric cancer) - Treated in the last 3 months or currently treated with therapy that interferes with the immune system (e.g. immunosuppressive therapy) - Current treatment with long-term corticosteroid therapy - Current treatment with long-term nonsteroidal anti-inflammatory drugs - Pregnant woman or breastfeeding - Patient or healthy volunteer under legal protection (e.g. guardianship) - Patient or healthy volunteer currently participating to a clinical trial evaluating either an experimental medical product or a medical device - Patient or healthy volunteer currently in custody Specific to Healthy Volunteer - Known history of Helicobacter pylori infection - Known history of gastric lesions (i.e. chronic gastritis, gastric atrophy, intestinal metaplasia, dysplasia and cancer) Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: Common * 18 years old or highter * written informed consent prior to any study procedure * Affiliated to a social insurance system Specific to patients with gastric lesions * Untreated glandular atrophy (with or without intestinal metaplasia and/or dysplasia) and histologically diagnosed as of 2014 * Treatment naïve Gastric cancer (distal or proximal adenocarcinoma) Exclusion Criteria: Common * Autoimmune disease or disease that impacts the immune system (e.g: HIV) * Chronic inflammatory disease * Known evolutive cancer (excluding gastric cancer) * Treated in the last 3 months or currently treated with therapy that interferes with the immune system (e.g. immunosuppressive therapy) * Current treatment with long-term corticosteroid therapy * Current treatment with long-term nonsteroidal anti-inflammatory drugs * Pregnant woman or breastfeeding * Patient or healthy volunteer under legal protection (e.g. guardianship) * Patient or healthy volunteer currently participating to a clinical trial evaluating either an experimental medical product or a medical device * Patient or healthy volunteer currently in custody Specific to Healthy Volunteer * Known history of Helicobacter pylori infection * Known history of gastric lesions (i.e. chronic gastritis, gastric atrophy, intestinal metaplasia, dysplasia and cancer)

Treatments Being Tested

PROCEDURE

Additional blood collection as part of a blood sampling performed during routine care or specific for the research if not part of routine care.

Collection of an additional blood volume (9 mL) as part of a blood sampling performed during routine care or specific for the research if not part of routine care.

PROCEDURE

Blood collection

Blood sample collection (10 mL)

Locations (8)

Ambroise Paré Teaching Hospital (AP-HP)
Boulogne-Billancourt, France
Beaujon Teaching Hospital (AP-HP)
Clichy, France
Kremlin Bicêtre Teaching Hospital (AP-HP)
Le Kremlin-Bicêtre, France
Cochin Teaching Hospital (AP-HP)
Paris, France
INVOLvE - Investigation et volontaires en santé humaine (Institut Pasteur)
Paris, France
Saint Antoine Teaching Hospital (AP-HP)
Paris, France
Saint Antoine Teaching Hospital (AP-HP)
Paris, France
Saint Louis Teaching Hospital (AP-HP)
Paris, France