To estimate the prevalence of histologically confirmed early gastric cancer (EGC) in an Indian multicentre cohort undergoing standardized high-quality upper gastrointestinal endoscopy. EGC is defined as gastric adenocarcinoma confined to the mucosa or submucosa (T1), irrespective of lymph node status, based on histopathology.
Gastric adenocarcinoma is a major global health problem and remains a leading cause of cancer-related mortality. Early detection significantly improves survival, with 5-year survival rates exceeding 80% in countries with established screening programmes, such as Japan (1) and South Korea (2). In contrast, most patients in India are diagnosed at advanced stages, resulting in poor outcomes. The Correa cascade (3) (4) describes a stepwise progression from chronic gastritis to atrophic gastritis, intestinal metaplasia (IM), dysplasia, and invasive adenocarcinoma. Helicobacter pylori infection is a major driver of this pathway. Identifying and characterising gastric precancerous lesions provides an opportunity for surveillance and early intervention. India lacks high-quality multicentre data on the prevalence and spectrum of gastric precancerous lesions and early gastric cancer. This study aims to systematically evaluate the gastric precancerous epithelial pathway using high-definition endoscopy and standardised histopathology across multiple centres in India.
Study Type
OBSERVATIONAL
Enrollment
4,000
AIG Hospitals
Hyderabad, Telangana, India
Prevalence of histologically confirmed early gastric cancer
Prevalence (proportion) of histologically confirmed early gastric cancer (EGC) detected on biopsy or endoscopic resection specimen during the endoscopy.
Time frame: 2 years
Prevalence of gastric precancerous lesions
Prevalence and distribution of gastric precancerous lesions, including: Atrophic gastritis, Intestinal metaplasia (EGGIM positive: Yes/No; and histologic IM/OLGIM), Low-grade dysplasia (LGD), High-grade dysplasia (HGD), Advanced precancerous phenotype (OLGIM III-IV and/or HGD)
Time frame: 2 years
Clinical and demographic predictors
Predictors of precancerous lesions
Time frame: 2 years
Endoscopy-pathology concordance
Endoscopy-pathology concordance, including concordance between: Endoscopic suspicion and histology
Time frame: 2 years
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