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

被引:38
作者
Ungureanu, Bogdan Silviu [1 ]
Lungulescu, Cristian-Virgil [2 ]
Pirici, Daniel [3 ]
Turcu-Stiolica, Adina [4 ]
Gheonea, Dan Ionut [1 ]
Sacerdotianu, Victor Mihai [1 ]
Liliac, Ilona Mihaela [3 ]
Moraru, Emil [5 ]
Bende, Felix [6 ]
Saftoiu, Adrian [1 ]
机构
[1] Univ Med & Pharm Craiova, Dept Gastroenterol, Craiova, Romania
[2] Univ Med & Pharm Craiova, Dept Oncol, Craiova, Romania
[3] Univ Med & Pharm Craiova, Dept Histol, Craiova, Romania
[4] Univ Med & Pharm Craiova, Pharmacoecon Dept, Craiova, Romania
[5] Univ Med & Pharm Craiova, Dept Surg, Craiova, Romania
[6] Univ Med & Farm Timisoara, Dept Gastroenterol, Timisoara, Romania
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
关键词
claudin; 18.2; gastric cancer; TNM stages; HER2; Lauren classification; THERAPY; STOMACH; TARGET;
D O I
10.3389/fonc.2021.643872
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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页数:11
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