Wu Jingxun, Wu Xuan, Liang Wenhua, Chen Chunling, Zheng Lingling, An Hanxiang
Department of Medical Oncology, The First Affiliated Hospital of Xiamen University, 55 Zhenhai Road, Xiamen, Fujian, 361000, People's Republic of China.
Tumour Biol. 2014 Apr;35(4):3709-15. doi: 10.1007/s13277-013-1490-8. Epub 2013 Dec 11.
The prognostic significance of CXC chemokine receptor type 4 (CXCR4) for survival of patients with esophageal cancer remains controversial. To investigate its expression impact on clinicopathological features and survival outcome, a meta-analysis was performed. A comprehensive search in the PubMed, Embase, and Web of Science (up to October 8, 2013) was performed for relevant studies using multiple search strategies. Correlation between CXCR4 expression and clinicopathological features and overall survival (OS) was analyzed. A total of 1,055 patients with esophageal cancer from seven studies were included. The pooled odds ratios (ORs) which indicated CXCR4 expression was associated with tumor depth (OR = 0.35, confidence interval (CI) = 0.27-0.47, P < 0.00001), status of lymph node (OR = 0.36, CI = 0.21-0.61, P < 0.0002), TNM (tumor, node, metastasis) stage (OR = 0.38, CI = 0.25-0.56, P < 0.00001), and histological type (OR = 1.81, CI = 1.07-3.05, P = 0.03). Poor overall survival of esophageal cancer was found to be significantly related to CXCR4 overexpression (hazard ratio (HR) 1.49, 95% CI = 1.24-1.80, P < 0.0001), whereas combined ORs exhibited that CXCR4 expression has no correlation with gender or tumor differentiation. Based on the published studies, CXCR4 overexpression in patients with esophageal cancer indicated worse survival outcome and was associated with common clinicopathological poor prognostic factors.
CXC趋化因子受体4(CXCR4)对食管癌患者生存的预后意义仍存在争议。为了研究其表达对临床病理特征和生存结果的影响,进行了一项荟萃分析。使用多种检索策略在PubMed、Embase和科学网(截至2013年10月8日)中全面检索相关研究。分析CXCR4表达与临床病理特征及总生存期(OS)之间的相关性。纳入了来自7项研究的共1055例食管癌患者。汇总比值比(OR)表明CXCR4表达与肿瘤深度相关(OR = 0.35,置信区间(CI)= 0.27 - 0.47,P < 0.00001)、淋巴结状态(OR = 0.36,CI = 0.21 - 0.61,P < 0.0002)、TNM(肿瘤、淋巴结、转移)分期(OR = 0.38,CI = 0.25 - 0.56,P < 0.00001)和组织学类型(OR = 1.81,CI = 1.07 - 3.05,P = 0.03)。发现食管癌患者总生存期差与CXCR4过表达显著相关(风险比(HR)1.49,95% CI = 1.24 - 1.80,P < 0.0001),而合并OR显示CXCR4表达与性别或肿瘤分化无关。基于已发表的研究,食管癌患者中CXCR4过表达表明生存结果较差,并与常见的临床病理不良预后因素相关。