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Prognostic and clinical significance of modified glasgow prognostic score in pancreatic cancer: a meta-analysis of 4629 patients

机译:修饰胰腺癌预后评分的预后及临床意义:4629例患者的META分析

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摘要

In this study, we evaluated the association of modified Glasgow Prognostic Score (mGPS) with prognosis in pancreatic cancer (PC) by performing a meta-analysis. Potentially eligible studies were shortlisted by searching PubMed, Embase, Web of Science, Scopus, and the Cochrane Library. A total of 4,629 patients with PC from 25 studies were finally included in this meta-analysis. Meta-analyses were performed using a random-effects model or fixed-effect model according to heterogeneity. We pooled the hazard ratios (HRs) with 95% confidence intervals (CIs) to estimate the association between mGPS and overall survival (OS). The results showed that elevated mGPS correlated with poor OS in patients with PC (HR=1.92, 95% CI=1.60–2.30, p<0.002). In addition, subgroup analysis indicated that increased mGPS remained a significant prognostic factor irrespective of the study design, region, disease status, treatment, survival analysis, cancer type, study center, or the Newcastle-Ottawa Scale (NOS) score (all p<0.05). There was a significant correlation between higher mGPS and male gender (Odds ratio [OR]=1.30, 95% CI=1.01–1.67, p=0.038). Elevated pretreatment mGPS is a marker of poor prognosis in patients with PC. As an easily available and cost-effective inflammatory parameter, mGPS can serve as a promising tool for prognostication in PC.
机译:在这项研究中,通过进行META分析,我们评估了改性的Glasgow预后评分(MGPS)在胰腺癌(PC)中的预后协会。潜在的符合条件的研究通过搜索PubMed,Embase,Scopus和Cochrane图书馆搜索。在该荟萃分析中,最终将共有来自25项研究的4,629名PC患者。使用根据异质性的随机效应模型或固定效果模型进行META分析。我们将危险比(HRS)汇集为95%的置信区间(CIS)来估计MGP和整体存活之间的关联(OS)。结果表明,PC患者升高的MGP与差的患者差(HR = 1.92,95%CI = 1.60-2.30,P <0.002)。此外,亚组分析表明,随着研究设计,区域,疾病状态,治疗,存活分析,癌症类型,学习中心或纽卡斯尔 - 渥太华规模(NOS)得分而言,亚组分析仍然存在显着的预后因素(所有P < 0.05)。较高的MGP和男性性别之间存在显着的相关性(少量比[或] = 1.30,95%CI = 1.01-1.67,P = 0.038)。预处理MGPS是PC患者预后不良的标志。作为一种易于可用和经济高效的炎症参数,MGPS可以作为PC预后的有希望的工具。

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