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SUrveillance of PREMalignant Stomach - Individualized Endoscopic Follow-up

Not Applicable
Recruiting
Conditions
Intestinal Metaplasia
Gastric Dysplasia
Gastric Cancer
Atrophic Gastritis
Interventions
Diagnostic Test: Upper gastrointestinal endoscopy
Registration Number
NCT04613570
Lead Sponsor
Instituto Portugues de Oncologia, Francisco Gentil, Porto
Brief Summary

Introduction: Gastric atrophy and intestinal metaplasia are the principal precursors for gastric cancer and, therefore, are considered gastric premalignant conditions. Although current guidelines recommend surveillance of individuals with these conditions, the best method for its identification and staging (histological vs endoscopy) and the best time schedule for follow-up are still controversial. Aims: To describe for the first-time patients with premalignant conditions both clinically (familial history), histologically (OLGA/OLGIM; complete/incomplete metaplasia) and endoscopically (EGGIM) using validated scales and to describe evolution of these parameters through time. To estimate prospectively the gastric cancer risk according to EGGIM stages. To define the best endoscopic surveillance follow-up for the several stages considering clinical, histological and endoscopic factors.

Methods: Multicenter study involving different gastroenterology departments from several countries. Consecutive patients older than 45 years scheduled for upper endoscopy in each of these centers will be evaluated by High-Resolution- endoscopy with virtual chromoendoscopy and EGGIM will be calculated. Guided biopsies (if areas suspicious of IM) and/or random biopsies (if no areas suspicious of IM) in antrum and corpus will be made and OLGA/OLGIM stages calculated. Patients will be evaluated in clinical consultation and database will be fulfilled. All patients will be eradicated for Helicobacter pylori infection if positive. At that occasion, all the patients with EGGIM\>5 and/or OLGA III/IV and/or OLGIM III/IV will be randomized for yearly (12 to 16 months) or every three years (32-40 months) endoscopic follow-up during a period of 6 years (SUPREME I). Endoscopic observational follow-up will be scheduled for patients with EGGIM 1-4 and OLGIM I/II at 3 and 6 years (SUPREME II). For individuals with no evidence of IM (EGGIM 0 and OLGIM 0, OLGA 0-II) a follow-up endoscopy 6 years after will be proposed (SUPREME III).

Detailed Description

Introduction: Gastric atrophy and intestinal metaplasia are the principal precursors for gastric cancer and, therefore, are considered gastric premalignant conditions. Although current guidelines recommend surveillance of individuals with these conditions, the best method for its identification and staging (histological vs endoscopy) and the best time schedule for follow-up are still controversial. Aims: To describe for the first-time patients with premalignant conditions both clinically (familial history), histologically (OLGA/OLGIM; complete/incomplete metaplasia) and endoscopically (EGGIM) using validated scales and to describe evolution of these parameters through time. To estimate prospectively the gastric cancer risk according to EGGIM stages. To define the best endoscopic surveillance follow-up for the several stages considering clinical, histological and endoscopic factors.

Methods: Multicenter study involving different gastroenterology departments from several countries. Consecutive patients older than 45 years scheduled for upper endoscopy in each of these centers will be evaluated by High-Resolution-endoscopy with virtual chromoendoscopy and EGGIM will be calculated. Guided biopsies (if areas suspicious of IM) and/or random biopsies (if no areas suspicious of IM) in antrum and corpus will be made and OLGA/OLGIM stages calculated. Patients will be evaluated in clinical consultation and database will be fulfilled. All patients will be eradicated for Helicobacter pylori infection if positive. At that occasion, all the patients with EGGIM\>5 and/or OLGA III/IV and/or OLGIM III/IV will be randomized for yearly (12 to 16 months) or every three years (32-40 months) endoscopic follow-up during a period of 6 years (SUPREME I). Endoscopic observational follow-up will be scheduled for patients with EGGIM 1-4 and OLGIM I/II at 3 and 6 years (SUPREME II). For individuals with no evidence of IM (EGGIM 0 and OLGIM 0, OLGA 0-II) a follow-up endoscopy 6 years after will be proposed (SUPREME III).

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
912
Inclusion Criteria
  • Patients scheduled for upper GI endoscopy with indication for gastric biopsies, including those with known gastric pathology (e.g. auto-immune gastritis) or premalignant conditions (e.g patients under surveillance because of atrophic gastritis);
  • Age above 45 years old
Exclusion Criteria
  • History of previous gastrectomy;
  • History of endoscopic resection of neoplastic lesion
  • History of previous gastric dysplasia (even with no detectable lesion)
  • Hereditary syndromes that increase gastric cancer risk (familial adenomatous polyposis; Lynch syndrome)
  • Serious comorbidities (ASA 3 or more)
  • Medication with anticoagulants

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Yearly endoscopyUpper gastrointestinal endoscopyUpper gastrointestinal endoscopy every year (12-16 months)
Endoscopy every 3 yearsUpper gastrointestinal endoscopyUpper gastrointestinal endoscopy every three years (32-40 months)
Primary Outcome Measures
NameTimeMethod
Carcinoma6 years

Proportion of patients with gastric adenocarcinoma

Dysplasia6 years

Proportion of patients with dysplasia (low or high-grade)

Secondary Outcome Measures
NameTimeMethod
Non-curative criteria6 years

Proportion of patients with submucosal, diffuse type or intramucosal carcinoma with high-risk criteria ("non-curative" criteria)

Advanced gastric cancer6 years

Proportion of patients with advanced gastric cancer (without indication for endoscopic treatment)

Curative criteria6 years

Proportion of patients with intramucosal carcinoma with low-risk criteria ("curative" criteria)

Trial Locations

Locations (1)

IPO-Porto

🇵🇹

Porto, Portugal

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