Tan Zhibo, Shen Weixi
Department of Oncology, Shenzhen Hospital of Southern Medical University, Shenzhen, Guangdong, P.R. China.
Oncotarget. 2017 Apr 18;8(16):27137-27144. doi: 10.18632/oncotarget.15648.
B7 homolog 4 (B7-H4) has been recently reported to be a prognostic marker in non-small cell lung cancer (NSCLC) in some studies. However, the results remained conflicting. Thus, we aimed to comprehensively assess the association between B7-H4 expression and prognosis of NSCLC patients by performing a meta-analysis. Relevant publications were thoroughly searched of PubMed, Embase, Web of Science and China National Knowledge Infrastructure (CNKI). The pooled odds ratios (ORs) and hazard ratios (HRs) with 95% confidence intervals (CIs) were applied to evaluate the effects. A total of 9 studies comprising 1444 patients were included in this meta-analysis. B7-H4 overexpression was associated with presence of lymph node metastasis (OR=3.59, 95%CI=2.39-5.38, p<0.001; fixed effect), advanced TNM stage (OR=2.36, 95%CI=1.2-4.67, p=0.013; random effect), and poor differentiation (OR=2.11, 95%CI=1.12-3.99, p=0.021; fixed effect). However, B7-H4 had no significant correlation with gender, age or histology in NSCLC. Furthermore, in a fixed effects model, the results indicated that B7-H4 overexpression was significantly associated with poor OS (HR=2.03, 95%CI=1.41-2.92, p<0.001). This meta-analysis demonstrated that high B7-H4 expression is an unfavorable prognostic factor in NSCLC. Because few studies were included for meta-analysis and almost all included studies were performed on Chinese patients, therefore; large scale prospective studies are needed to verify our results.
近期一些研究报道称,B7同源物4(B7-H4)是非小细胞肺癌(NSCLC)的一种预后标志物。然而,结果仍存在矛盾。因此,我们旨在通过进行一项荟萃分析,全面评估B7-H4表达与NSCLC患者预后之间的关联。我们对PubMed、Embase、科学网和中国知网(CNKI)进行了全面的相关文献检索。采用合并比值比(OR)和风险比(HR)以及95%置信区间(CI)来评估效应。本荟萃分析共纳入9项研究,涉及1444例患者。B7-H4过表达与淋巴结转移(OR = 3.59,95%CI = 2.39 - 5.38,p < 0.001;固定效应)、晚期TNM分期(OR = 2.36,95%CI = 1.2 - 4.67,p = 0.013;随机效应)以及低分化(OR = 2.11,95%CI = 1.12 - 3.99,p = 0.021;固定效应)相关。然而,B7-H4与NSCLC患者的性别、年龄或组织学无显著相关性。此外,在固定效应模型中,结果表明B7-H4过表达与较差的总生存期显著相关(HR = 2.03,95%CI = 1.41 - 2.92,p < 0.001)。这项荟萃分析表明,高B7-H4表达是NSCLC的一个不良预后因素。由于纳入荟萃分析的研究较少,且几乎所有纳入研究均针对中国患者进行,因此,需要大规模的前瞻性研究来验证我们的结果。
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