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Staging of intestinal- and diffuse-type gastric cancers with the OLGA and OLGIM staging systems

机译:OLGA和OLGIM分期系统对肠型和弥漫型胃癌的分期

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Background Operative link on gastritis assessment (OLGA) and Operative link on gastric intestinal metaplasia assessment (OLGIM) staging systems have been proposed for gastric cancer (GC) risk estimation. Aim To validate the OLGA and OLGIM staging systems in a region with high risk of GC. Methods This retrospective study included 474 GC patients and age- and sex-matched health screening control persons in a cancer centre hospital. We classified gastritis patterns according to the OLGA and OLGIM systems using the histological database that a pathologist prospectively evaluated using the updated Sydney system. GC risk according to the OLGA and OLGIM stages was evaluated using logistic regression analysis. Results More GC patients had OLGA stages III-IV (46.2%) than controls (26.6%, P < 0.001), particularly among patients with intestinal-type GCs (62.2%) compared with diffuse-type GCs (30.9%). OLGA stages III and IV were significantly associated with increased risk of GC [odds ratios (ORs), 2.09; P = 0.008 and 2.04; P = 0.014 respectively] in multivariate analysis. The association was more significant for intestinal-type (ORs, 4.76; P = 0.001 and 4.19; P = 0.002 respectively), but not diffuse-type GC. OLGIM stages from I to IV were significantly associated with increased risk of both intestinal-type (ORs, 3.64, 5.15, 7.89 and 13.20 respectively) and diffuse-type GC (ORs, 1.84, 2.59, 5.08 and 6.32 respectively) with a significantly increasing trend. Conclusion As high OLGA and OLGIM stages are independent risk factors for gastric cancer, the staging systems may be useful for risk assessment in high-risk regions, especially for intestinal-type gastric cancer.
机译:背景技术已提出胃炎评估(OLGA)的手术链接和胃肠化生评估(OLGIM)分期系统的手术链接以评估胃癌(GC)风险。目的在具有高GC风险的地区验证OLGA和OLGIM分级系统。方法这项回顾性研究纳入了474名GC患者以及年龄和性别相匹配的健康筛查控制人员,这些患者均位于癌症中心医院。我们使用组织学数据库根据OLGA和OLGIM系统对胃炎类型进行分类,病理学家使用更新的Sydney系统对组织学数据库进行了前瞻性评估。使用逻辑回归分析评估了根据OLGA和OLGIM阶段的GC风险。结果GC病人的OLGA III-IV期(46.2%)比对照组(26.6%,P <0.001)多,尤其是肠型GC(62.2%)相比,弥散型GC(30.9%)。 OLGA III和IV期与GC风险增加显着相关[比值比(OR),2.09; P = 0.008和2.04; P分别为0.014]。肠型相关性更显着(OR,4.76; P = 0.001和4.19; P = 0.002),而不是弥散型GC。从I到IV的OLGIM分期与肠道型(分别为OR,3.64、5.15、7.89和13.20)和弥散型GC(分别为OR,1.84、2.59、5.08和6.32)的风险增加显着相关趋势。结论由于高OLGA和OLGIM分期是胃癌的独立危险因素,因此分期系统可能对高风险地区(尤其是肠型胃癌)的风险评估有用。

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