Histologic and serum risk markers for noncardia early gastric cancer
β Scribed by Akiko Shiotani; Hiroyasu Iishi; Noriya Uedo; Mitutaka Kumamoto; Yukinori Nakae; Shingo Ishiguro; Masaharu Tatsuta; David Y. Graham
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- French
- Weight
- 119 KB
- Volume
- 115
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Abstract
Corpus dominant gastritis and intestinal metaplasia (IM) are considered markers of increased risk of gastric carcinoma. The aim of our study was to determine serum and histologic risk markers of gastric cancer. Antral and corpus histology, pepsinogen and gastrin 17 levels were compared among patients with history of endoscopic mucosal resection (EMR) for early gastric cancer and controls. Serum pepsinogen (PG) and gastrin 17 levels were measured by RIA. There were 53 gastric cancer patients and 75 controls. The scores for IM in each region and atrophy at the lesser curvature of the corpus were significantly higher in the cancer group than in the H. pyloriβpositive control group. IM at the greater curvature of the corpus and atrophy at the lesser curvature of the corpus were associated with multiple malignant lesions. Although corpus gastritis was associated with an increased risk of gastric cancer (odds ratio [OR] = 3.4; 95% confidence interval [CI] 1.6β7.0) (p = 0.001), the most important marker was the presence of IM at the lesser curvature of the corpus (OR = 15.1; 95% CI 4.3β52.6) (p < 0.001)). The best cutβoff points of serum markers for gastric cancer were a PG I concentration of 45 ng/mL or less and a gastrin 17 >60 pg/mL (sensitivity = 83%; specificity = 68%). IM at the lesser curvature of the corpus and the combination of serum gastrin 17 and PG I identified a group at high risk for development of gastric cancer. Annual endoscopic followβup is warranted for patients with IM found at the greater curvature of the corpus. Β© 2005 WileyβLiss, Inc.
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