Chen Guodong, Li Xiaoyan, Yang Jing, Li Jie, Wang Xia, He Jun, Huang Zonghai
Department of General Surgery, First Affiliated Hospital, University of South China, Hengyang, China; Department of General Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Department of Endocrinology, Hengyang Central Hospital, Hengyang, China.
Arch Med Sci. 2016 Oct 1;12(5):1110-1117. doi: 10.5114/aoms.2016.61916. Epub 2016 Aug 24.
Cyclooxygenase-2 (COX-2) is believed to be an important enzyme in the carcinogenesis of hepatocellular carcinoma (HCC). However, it is still controversial whether COX-2 expression can be regarded as a prognostic factor for HCC patients. We performed a systematic review and meta-analysis of studies assessing the clinical and prognostic significance of COX-2 expression in HCC.
Identification and review of publications assessing clinical or prognostic significance of COX-2 expression in HCC until November 1, 2014. A meta-analysis was performed to clarify the association between COX-2 expression and clinical outcomes.
A total of 11 publications met the criteria and included 943 cases. Analysis of these data showed that COX-2 expression was not significantly correlated with capsular formation (OR = 0.84, 95% confidence interval (CI): 0.46-1.55, = 0.58), tumor TNM stage (OR = 0.73, 95% CI: 0.23-2.33, = 0.59), vascular invasion (OR = 1.04, 95% CI: 0.25-4.35, = 0.96), tumor size (OR = 0.78, 95% CI: 0.21-2.86, = 0.71), or tumor differentiation degree (OR = 1.08, 95% CI: 0.42-2.79, = 0.87). However, in the identified studies, COX-2 expression was strongly associated with high alpha-fetoprotein level (OR = 1.83, 95% CI: 1.01-3.33, = 0.05), HBsAg status (OR = 1.85, 95% CI: 1.13-3.03, = 0.01), decreased overall survival (relative risk (RR): 1.54, 95% CI: 1.18-2.02, = 0.001) and decreased disease-free survival (RR = 1.49, 95% CI: 1.22-1.81, < 0.001).
This meta-analysis shows that COX-2 expression in HCC is associated with decreased overall and disease-free survival and thus marks a worse prognosis. Nevertheless, more large sample and well-designed studies are warranted to confirm this finding.
环氧合酶-2(COX-2)被认为是肝细胞癌(HCC)致癌过程中的一种重要酶。然而,COX-2表达是否可被视为HCC患者的预后因素仍存在争议。我们对评估COX-2表达在HCC中的临床和预后意义的研究进行了系统综述和荟萃分析。
检索并综述截至2014年11月1日评估COX-2表达在HCC中的临床或预后意义的出版物。进行荟萃分析以阐明COX-2表达与临床结局之间的关联。
共有11篇出版物符合标准,纳入943例病例。对这些数据的分析表明,COX-2表达与包膜形成(比值比(OR)=0.84,95%置信区间(CI):0.46-1.55,P=0.58)、肿瘤TNM分期(OR = 0.73,95% CI:0.23-2.33,P = 0.59)、血管侵犯(OR = 1.04,95% CI:0.25-4.35,P = 0.96)、肿瘤大小(OR = 0.78,95% CI:0.21-2.86,P = 0.71)或肿瘤分化程度(OR = 1.08,95% CI:0.42-2.79,P = 0.87)均无显著相关性。然而,在纳入的研究中,COX-2表达与高甲胎蛋白水平(OR = 1.83,95% CI:1.01-3.33,P = 0.05)、乙肝表面抗原状态(OR = 1.85,95% CI:1.13-3.03,P = 0.01)、总生存期降低(相对危险度(RR):1.54,95% CI:1.18-2.02,P = 0.001)和无病生存期降低(RR = 1.49,95% CI:1.22-1.81,P<0.001)密切相关。
这项荟萃分析表明,HCC中的COX-2表达与总生存期和无病生存期降低相关,因此预示着更差的预后。然而,仍需要更多大样本且设计良好的研究来证实这一发现。