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OLGA 分期胃炎与胃癌风险:一项为期十二年的临床病理随访研究。

Gastritis OLGA-staging and gastric cancer risk: a twelve-year clinico-pathological follow-up study.

机构信息

Department of Diagnostic Medical Sciences and Special Therapies, University of Padova, Italy.

出版信息

Aliment Pharmacol Ther. 2010 May;31(10):1104-11. doi: 10.1111/j.1365-2036.2010.04277.x. Epub 2010 Feb 23.

DOI:10.1111/j.1365-2036.2010.04277.x
PMID:20180784
Abstract

BACKGROUND

Intestinal-type gastric cancer (GC) still ranks among the high-incidence, highly lethal malignancies. Atrophic gastritis is the cancerization field in which GC develops. The current histological reporting formats for gastritis do not include any (atrophy-based) ranking of GC risk.

AIM

To test the gastritis OLGA-staging (Operative Link for Gastritis Assessment) in prognosticating neoplastic progression.

METHODS

Ninety-three Italian patients were followed up for more than 12 years (range: 144-204 months). Clinical examinations, pepsinogen serology, endoscopy and histology (also assessing Helicobacter pylori status) were performed both at enrolment (T1) and at the end of the follow-up (T2).

RESULTS

All invasive or intra-epithelial gastric neoplasia were consistently associated with high-risk (III/IV) OLGA stages. There was a significant inverse correlation between the mean pepsinogen ratio and the OLGA stage (test for trend; P < 0.001). OLGA-staging at T1 predicted both the OLGA stage (Kaplan-Maier log-rank test, P = 0.001) and the neoplasia at T2 (Kaplan-Maier log-rank test, P = 0.001).

CONCLUSIONS

This long-term follow-up study provides the first evidence that gastritis OLGA-staging conveys relevant information on the clinico-pathological outcome of gastritis and therefore for patient management. According to OLGA-staging and H. pylori-status, gastritis patients could be confidently stratified and managed according to their different cancer risks.

摘要

背景

肠型胃癌(GC)仍然是高发病率和高致死率的恶性肿瘤之一。萎缩性胃炎是 GC 发生的癌前病变部位。目前的胃炎组织学报告格式不包括任何(基于萎缩的)GC 风险分级。

目的

测试胃炎 OLGA 分期(胃炎评估操作链接)在预测肿瘤进展方面的作用。

方法

93 名意大利患者接受了超过 12 年的随访(范围:144-204 个月)。在入组时(T1)和随访结束时(T2)进行了临床检查、胃蛋白酶原血清学、内窥镜检查和组织学检查(还评估了幽门螺杆菌状态)。

结果

所有侵袭性或上皮内胃肿瘤均与高风险(III/IV)OLGA 分期一致。平均胃蛋白酶原比值与 OLGA 分期呈显著负相关(趋势检验;P < 0.001)。T1 时的 OLGA 分期预测了 T2 时的 OLGA 分期(Kaplan-Meier 对数秩检验,P = 0.001)和肿瘤(Kaplan-Meier 对数秩检验,P = 0.001)。

结论

这项长期随访研究首次提供了证据,证明胃炎 OLGA 分期提供了与胃炎临床病理结果相关的信息,因此对患者管理具有重要意义。根据 OLGA 分期和 H. pylori 状态,可以对胃炎患者进行有信心的分层和管理,以适应他们不同的癌症风险。

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