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Evaluating the Reporting Transparency and Interpretability of OLGA and OLGIM Staging in Gastric Cancer Risk
Jing Tian1, Wenjie Xu1, Shaofen Xu1
1The First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, China.
Clinical and Translational Gastroenterology
|June 25, 2026
Summary
Reporting of OLGA/OLGIM for gastric cancer risk stratification varies. Incomplete details on biopsy sampling, grading, and stage derivation limit study comparability and reproducibility.
Area of Science:
- Gastroenterology and Hepatology
- Oncology
- Pathology
Background:
- The Operative Link for Gastritis Assessment (OLGA) and Operative Link for Intestinal Metaplasia (OLGIM) are utilized for gastric cancer risk stratification.
- Published studies often lack clarity in reporting the implementation of these staging systems.
- This variability impacts the reliability and comparability of research findings.
Purpose of the Study:
- To assess the interpretability of reporting for OLGA/OLGIM implementation in published studies.
- Focus on reporting transparency rather than methodological quality or guideline adherence.
Main Methods:
- Systematic literature search of PubMed, Embase, and Cochrane CENTRAL up to March 2026.
- Included studies applying OLGA and/or OLGIM with reported staging results.
- Reporting interpretability appraised using a framework assessing biopsy sampling, histological assessment, grading, and stage derivation.
Main Results:
- 155 studies were included; 48.4% showed high reporting interpretability, 46.5% moderate, and 5.2% low.
- Key details for understanding stage generation, including biopsy sampling, grading approach, and stage derivation, were frequently incomplete.
- Incomplete reporting limited the interpretability, reproducibility, and comparability of OLGA/OLGIM evidence.
Conclusions:
- Significant variability exists in the implementation reporting of OLGA and OLGIM.
- Limited interpretability often stems from incomplete reporting, not necessarily flawed methods.
- Enhanced transparency in reporting is crucial for improving reproducibility, cross-study comparison, and clinical translation of gastric cancer risk stratification.
