Prognostic Significance of the Modified Glasgow Prognostic Score in Patients With Pancreatic Cancer: A Meta-Analysis

Background: The prognostic value of the modified Glasgow prognostic score (mGPS) in patients with pancreatic cancer is controversial, based on previous studies. Therefore, this meta-analysis aimed to explore the relationship between mGPS and prognosis in pancreatic cancer. Methods: The databases Pub...

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Main Authors: Wen Fu (Author), Kun Wang (Author), Shan Yan (Author), Xie Wang (Author), Bo Tang (Author), Jiang Chang (Author), Ran Wang (Author), Tao Wu (Author)
Format: Book
Published: SAGE Publishing, 2020-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Wen Fu  |e author 
700 1 0 |a Kun Wang  |e author 
700 1 0 |a Shan Yan  |e author 
700 1 0 |a Xie Wang  |e author 
700 1 0 |a Bo Tang  |e author 
700 1 0 |a Jiang Chang  |e author 
700 1 0 |a Ran Wang  |e author 
700 1 0 |a Tao Wu  |e author 
245 0 0 |a Prognostic Significance of the Modified Glasgow Prognostic Score in Patients With Pancreatic Cancer: A Meta-Analysis 
260 |b SAGE Publishing,   |c 2020-07-01T00:00:00Z. 
500 |a 1559-3258 
500 |a 10.1177/1559325820942065 
520 |a Background: The prognostic value of the modified Glasgow prognostic score (mGPS) in patients with pancreatic cancer is controversial, based on previous studies. Therefore, this meta-analysis aimed to explore the relationship between mGPS and prognosis in pancreatic cancer. Methods: The databases PubMed, Web of Science, Embase, and the Cochrane Library were searched to identify eligible studies. Hazard ratios (HRs) and 95% confidence intervals (CIs) were used to estimate the associations between mGPS score and survival outcomes. Results: A total of 26 studies with 5198 patients were included in this meta-analysis. In a pooled analysis, elevated mGPS predicted poorer overall survival (OS; HR = 1.98, 95% CI, 1.65-2.37, P < .001). In addition, elevated mGPS was also significantly associated with worse progression-free survival (PFS), disease-free survival (DFS), and cancer-specific survival (CSS; HR = 1.95, 95% CI, 1.36-2.80, P < .001). Subgroup analyses confirmed a significant association between mGPS and survival outcomes. Conclusions: Our meta-analysis demonstrated that high mGPS was correlated to worse OS, PFS, DFS, and CSS in patients with pancreatic cancer. Therefore, mGPS could be employed as an effective prognostic factor for pancreatic cancer in clinical practice. 
546 |a EN 
690 |a Therapeutics. Pharmacology 
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786 0 |n Dose-Response, Vol 18 (2020) 
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