Modified Glasgow prognostic score as a marker for predicting outcomes in patients with either bladder and prostate cancer : A systematic review and meta-analysis.

IF 2.5 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2025-03-28 DOI:10.1159/000545001
Jie Chen, Suna Fu, Jianhong Yu, Qi Tang, Xiuping Wu, Sai Luo, Huifang Sun
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引用次数: 0

Abstract

Objective: To investigate the association of pretreatment-modified Glasgow Prognostic Score (mGPS) with survival-related outcomes in patients with bladder cancer (BC) and prostate cancer (PC).

Methods: A systematic search was performed in PubMed, EMBASE, Web of Science, and Scopus databases for cohort studies in adult participants (≥18 years). The exposure was pre-treatment mGPS and the outcomes of interest were overall survival (OS), cancer-specific survival (CSS), and recurrence-free survival (RFS). Eligible studies compared low mGPS (considered as a score of 0) with a score of ≥1. A random effects model was used for the analysis. Pooled effect sizes were reported as hazard ratio (HR) with 95% confidence intervals (CI). Subgroup analysis was performed based on the tumour stage (≤T2 and >T2), sample size (≥200 and <200), treatment (surgical and non-surgical), and the Newcastle-Ottawa Scale (NOS) score (≥8 and ≤7).

Results: Of 20 studies. Included in the analysis, 19 studies were retrospective cohort studies. Fourteen studies reported data of patients with BC, and the remaining 6 studies focused on PC patients. Compared to mGPS of 0, higher scores were associated with reduced OS (HR 2.65, 95% CI: 1.99, 3.52), CSS (HR 1.64, 95% CI: 1.19, 2.26), and RFS (HR 1.77, 95% CI: 1.50, 2.08). There was no evidence of publication bias (Egger's p>0.05). These associations remained valid in subgroup analysis.

Conclusion: Higher mGPS values were found to be associated with significantly reduced survival outcomes. These findings underscore the prognostic significance of mGPS, thereby highlighting its potential clinical utility in risk stratification and treatment decision-making.

目的研究膀胱癌(BC)和前列腺癌(PC)患者治疗前修正格拉斯哥预后评分(mGPS)与生存相关结果的关系:在 PubMed、EMBASE、Web of Science 和 Scopus 数据库中对成年参与者(≥18 岁)的队列研究进行了系统检索。研究对象为治疗前的 mGPS,研究结果为总生存期(OS)、癌症特异性生存期(CSS)和无复发生存期(RFS)。符合条件的研究对低 mGPS(0 分)和≥1 分进行了比较。汇总效应大小以危险比 (HR) 和 95% 置信区间 (CI) 的形式报告。根据肿瘤分期(≤T2 和 >T2)、样本量(≥200 和 结果)进行分组分析:在 20 项研究中。19项研究为回顾性队列研究。14 项研究报告了 BC 患者的数据,其余 6 项研究主要针对 PC 患者。与 mGPS 为 0 相比,得分越高,OS(HR 2.65,95% CI:1.99,3.52)、CSS(HR 1.64,95% CI:1.19,2.26)和 RFS(HR 1.77,95% CI:1.50,2.08)越低。没有证据表明存在发表偏倚(Egger's p>0.05)。这些关联在亚组分析中仍然有效:结论:mGPS值越高,生存率越低。这些发现强调了 mGPS 的预后意义,从而突出了其在风险分层和治疗决策中的潜在临床用途。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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