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Claudin 18.2在胃癌中的表达与临床病理相关性的Meta分析

Clinicopathologic Relevance of Claudin 18.2 Expression in Gastric Cancer: A Meta-Analysis.

作者信息

Ungureanu Bogdan Silviu, Lungulescu Cristian-Virgil, Pirici Daniel, Turcu-Stiolica Adina, Gheonea Dan Ionut, Sacerdotianu Victor Mihai, Liliac Ilona Mihaela, Moraru Emil, Bende Felix, Saftoiu Adrian

机构信息

Gastroenterology Department, University of Medicine and Pharmacy of Craiova, Craiova, Romania.

Oncology Department, University of Medicine and Pharmacy of Craiova, Craiova, Romania.

出版信息

Front Oncol. 2021 Mar 4;11:643872. doi: 10.3389/fonc.2021.643872. eCollection 2021.

Abstract

An increasing number of tumor markers have been discovered to have potential efficacy as diagnostic and prognostic tools in gastric cancer. We aimed to assess putative correlations between claudin 18.2 expression and pathological or prognosis features in patients with gastric cancer. MEDLINE, Web of Science, EBSCO, and ClinicalTrials.gov were used to search for relevant studies from their inception to 30 October 2020. Finally, a total of six articles were included in this meta-analysis. Review Manager 5 software was applied to examine the heterogeneity among the studies and to calculate the odds ratio with 95% CI by selecting corresponding models, in evaluating the strength of the relationship. Publication bias test was also conducted. No bias and no significant correlations were found between CLDN 18.2 and TNM stages, Lauren classification, HER2, grading, or overall survival. This meta-analysis expounded that the relationship with CLDN 18.2 and pathological features depends on the percentage of staining of tumor cells for which CLDN 18.2 is considered positive. Our pooled outcomes suggest that targeted therapy for CLDN 18.2 could be effective if certain criteria were established.

摘要

越来越多的肿瘤标志物被发现作为胃癌诊断和预后工具具有潜在疗效。我们旨在评估claudin 18.2表达与胃癌患者病理或预后特征之间的假定相关性。使用MEDLINE、Web of Science、EBSCO和ClinicalTrials.gov从各数据库建库至2020年10月30日检索相关研究。最终,本荟萃分析共纳入6篇文章。应用Review Manager 5软件检查各研究间的异质性,并通过选择相应模型计算95%置信区间的比值比,以评估关系强度。还进行了发表偏倚检验。未发现CLDN 18.2与TNM分期、Lauren分类、HER2、分级或总生存期之间存在偏倚和显著相关性。本荟萃分析表明,CLDN 18.2与病理特征的关系取决于将CLDN 18.2视为阳性的肿瘤细胞染色百分比。我们汇总的结果表明,如果建立某些标准,针对CLDN 18.2的靶向治疗可能有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5df/7969651/f507e959c94a/fonc-11-643872-g0001.jpg

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