c反应蛋白及其与白蛋白的比值作为口腔癌不良预后的标志:一项系统综述和荟萃分析

IF 2.2
Jiating Xuan, Xiaoqing Ma
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引用次数: 0

摘要

目的:探讨c反应蛋白(CRP)和CRP-白蛋白比(CAR)对口腔癌预后的影响。方法:检索PubMed、Scopus、Embase和Web of Science数据库中报告CRP或CAR与口腔癌患者总生存期(OS)或无病生存期(DFS)相关的研究。搜寻工作于2024年12月13日结束。进行随机效应荟萃分析。结果:共纳入11项研究(6项关于CRP, 5项关于CAR)。荟萃分析显示,高CRP水平与口腔癌患者较差的OS生存率(HR: 1.80 95% CI: 1.11, 2.92 I2 = 80%)和DFS (HR: 1.81 95% CI: 1.28, 2.56 I2 = 0%)相关。合并分析还显示,高CAR与低OS (HR: 3.15 95% CI: 2.25, 4.42 I2 = 0%)和DFS (HR: 2.50 95% CI: 1.38, 4.55 I2 = 19%)之间存在统计学上的显著关系。基于CRP的OS结果在敏感性和亚组分析上并不稳健。然而,基于CAR的OS在敏感性和亚组分析上没有发现结果的显著性变化。结论:CRP和CAR均可作为预测口腔癌术后生存的潜在生物标志物。CAR观察到更强的相关性和更好的稳定性。研究数量少和研究间异质性高是现有证据的局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C-reactive protein and its ratio with albumin as a marker of poor prognosis in oral cancer: a systematic review and meta-analysis.

Objective: This review aims to examine the prognostic ability of C-reactive protein (CRP) and CRP-albumin ratio (CAR) for oral cancer.

Methods: Repositories of PubMed, Scopus, Embase, and Web of Science were searched for studies reporting an association between CRP or CAR and overall survival (OS) or disease-free survival (DFS) in oral cancer patients. The search ended on 13th December 2024. Random-effects meta-analysis was conducted.

Results: A total of 11 studies (six on CRP and five on CAR) were included. Meta-analysis showed that high CRP levels were associated with worse OS survival (HR: 1.80 95% CI: 1.11, 2.92 I2 = 80%) and DFS in oral cancer patients (HR: 1.81 95% CI: 1.28, 2.56 I2 = 0%). The pooled analysis also showed a statistically significant relationship between high CAR and poor OS (HR: 3.15 95% CI: 2.25, 4.42 I2 = 0%) and DFS (HR: 2.50 95% CI: 1.38, 4.55 I2 = 19%). Results of OS based on CRP were not robust on sensitivity and subgroup analysis. However, no change in the significance of results was noted for OS based on CAR on sensitivity and subgroup analysis.

Conclusions: Both CRP and CAR could be potential biomarkers for predicting survival after oral cancer. Stronger association and better stability of results were seen with CAR. The low number of studies and high interstudy heterogeneity are limitations of current evidence.

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