Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, 69 Meishan Road, Hefei, 230032, Anhui Province, China.
Dig Dis Sci. 2014 Feb;59(2):436-45. doi: 10.1007/s10620-013-2917-1. Epub 2013 Nov 1.
Cyclooxygenase-2 (COX-2) is believed to be involved in gastric carcinogenesis. However, it is still controversial whether COX-2 expression can be regarded as a prognostic factor for gastric cancer patients.
To obtain a more accurate relationship between COX-2 overexpression and prognosis in gastric cancer by meta-analysis.
Relevant articles published up to May 2013 were searched by use of several keywords in electronic databases. Separate hazard ratio (HR) estimates and 95 % confidence intervals (95 % CI) for COX-2 overexpression and overall survival (OS) and disease-free survival (DFS) with gastric cancer were extracted. Combined HR with 95 % CI was calculated by use of Stata11.0 software to estimate the size of the effect. Publication bias testing and sensitivity analysis were also performed.
A total of 27 studies which included 3,891 gastric cancer patients were combined in the final analysis. Combined results suggested that COX-2 overexpression was associated with an unfavorable OS (HR 1.58, 95 % CI 1.36-1.84) but not DFS (HR 1.15, 95 % CI 0.93-1.43) among patients with gastric cancer. Publication bias was absent. Sensitivity analysis suggested that the results of this meta-analysis were robust.
The results of this meta-analysis suggest that high COX-2 expression may be an independent risk factor for poor OS of patients with gastric cancer. More large prospective studies are now needed to further clarify the prognostic value of COX-2 expression for DFS in gastric cancer.
环氧化酶-2(COX-2)被认为与胃癌的发生有关。然而,COX-2 表达是否可以作为胃癌患者的预后因素仍存在争议。
通过荟萃分析获得 COX-2 过表达与胃癌预后之间更准确的关系。
使用电子数据库中的几个关键词搜索截至 2013 年 5 月发表的相关文章。提取 COX-2 过表达与总生存期(OS)和无病生存期(DFS)与胃癌相关的单独风险比(HR)估计值和 95%置信区间(95%CI)。使用 Stata11.0 软件计算合并 HR 及其 95%CI,以评估效应大小。还进行了发表偏倚检验和敏感性分析。
共有 27 项研究,包括 3891 例胃癌患者,最终纳入了分析。合并结果表明,COX-2 过表达与 OS 不良相关(HR 1.58,95%CI 1.36-1.84),但与 DFS 无关(HR 1.15,95%CI 0.93-1.43)。无发表偏倚。敏感性分析表明,该荟萃分析的结果是稳健的。
这项荟萃分析的结果表明,COX-2 过表达可能是胃癌患者 OS 不良的独立危险因素。目前需要更多的大型前瞻性研究来进一步阐明 COX-2 表达对胃癌 DFS 的预后价值。