Department of Thoracic Surgery, Chengdu First People's Hospital, Chengdu, China.
Biomarkers. 2024 Mar;29(2):105-113. doi: 10.1080/1354750X.2024.2319702. Epub 2024 Feb 29.
Although Osteopontin (OPN) has been reported to be associated with many different human cancers, the data on non-small cell lung cancer (NSCLC) are not definitive. This study aimed to explore the prognostic effect of OPN expression and clinicopathological characteristics in patients with NSCLC.
This study followed all aspects of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) report. PubMed, Embase and the Cochrane Library were searched to identify the relative studies. The pooled hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to estimate the prognostic value of the OPN in patients with NSCLC. The odds ratio (OR) was calculated to represent the relationship between OPN expression and clinicopathological parameters.
A total of fifteen studies with 2173 participants were finally included. The results revealed that high expression of OPN was significantly associated with poorer overall survival (OS) (HR = 1.89; 95%CI = 1.68-2.11; p < 0.001). Moreover, a significant correlation was observed between increased OPN expression and poorly differentiated (well and moderately differentiated vs. poorly differentiated; pooled OR = 0.38; 95% CI = 0.23-0.64; p < 0.001), lymph node metastasis (absence vs. presence; pooled OR = 0.49; 95%CI = 0.32-0.74; p < 0.001), and distant metastasis (absence vs. presence; pooled OR = 0.18; 95%CI = 0.11-0.29; p < 0.001).
This meta-analysis implies that OPN might be a valuable biomarker for a poor prognosis and poor clinicopathological outcomes for patients with NSCLC.
尽管骨桥蛋白(OPN)已被报道与许多不同的人类癌症有关,但关于非小细胞肺癌(NSCLC)的数据并不明确。本研究旨在探讨 OPN 表达与 NSCLC 患者临床病理特征的关系及其预后意义。
本研究遵循系统评价和荟萃分析的首选报告项目(PRISMA)报告的各个方面。通过检索 PubMed、Embase 和 Cochrane 图书馆,确定了相关研究。通过计算合并风险比(HR)和 95%置信区间(CI)来评估 OPN 在 NSCLC 患者中的预后价值。通过计算比值比(OR)来表示 OPN 表达与临床病理参数之间的关系。
共纳入了 15 项研究,总计 2173 名参与者。结果表明,OPN 高表达与总生存期(OS)较差显著相关(HR=1.89;95%CI=1.68-2.11;p<0.001)。此外,OPN 表达增加与低分化(高、中分化与低分化;合并 OR=0.38;95%CI=0.23-0.64;p<0.001)、淋巴结转移(无 vs. 有;合并 OR=0.49;95%CI=0.32-0.74;p<0.001)和远处转移(无 vs. 有;合并 OR=0.18;95%CI=0.11-0.29;p<0.001)显著相关。
本荟萃分析表明,OPN 可能是 NSCLC 患者预后不良和临床病理结局不佳的有价值的生物标志物。