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y The Prognostic Effect of Dexamethasone on Patients With Glioblastoma: A Systematic Review and Meta-Analysis
被引:17
作者:
Zhou, Lingling
[1
]
Shen, Yang
[2
]
Huang, Tingting
[3
]
Sun, Yangyang
[4
]
Alolga, Raphael N.
[4
]
Zhang, Gang
[3
]
Ge, Yuqiu
[5
]
机构:
[1] Nanjing Med Univ, Dept Orthopaed Surg, Childrens Hosp, Nanjing, Peoples R China
[2] Nanjing Univ Chinese Med, Dept Urol, Affiliated Hosp 2, Nanjing, Peoples R China
[3] Nanjing Med Univ, Dept Neurol, Childrens Hosp, Nanjing, Peoples R China
[4] China Pharmaceut Univ, Clin Metabol Ctr, Nanjing, Peoples R China
[5] Jiangnan Univ, Wuxi Sch Med, Dept Publ Hlth & Prevent Med, Wuxi, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
dexamethasone;
glioblastoma;
prognosis;
epidemiology;
meta-analysis;
POTASSIUM CHANNEL EXPRESSION;
METASTATIC BRAIN-TUMORS;
SURVIVAL;
BARRIER;
EDEMA;
GLIOMAS;
IMPACT;
D O I:
10.3389/fphar.2021.727707
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Background: Dexamethasone (DEX) is widely adopted to reduce tumor-associated edema in glioblastoma (GBM) patients despite its side effects. However, the benefits of using DEX in GBM patients remains elusive. Methods: In this study, we performed a comprehensive meta-analysis to address this concern. We searched the relevant studies from PubMed, Web of Science, and EMBASE databases, and then applied random or fixed-effects models to generate estimated summary hazard radios (HRs) and the 95% confidence intervals (CIs). Moreover, subgroup and sensitivity analysis were conducted and publication bias were further evaluated. Results: Ten articles with a total of 2,230 GBM patients were eligible according to the inclusion criteria. In the assessment of overall survival (OS), meta-analysis data revealed that DEX was significantly associated with the poor prognosis of GBM patients (HR=1.44, 95% CI=1.32-1.57). In the progression-free survival (PFS), the pooled results indicated that the use of DEX can increase 48% death risk for GBM patients (HR=1.48, 95% CI=1.11-1.98). Subgroup analyses revealed that DEX was associated with poorer outcome of GBM in subgroup of newly diagnosed patients and GBM patients treated with >= 2mg/day. Sensitivity analyses showed that no study changed the pooled results materially for both OS and PFS analyses. The funnel plot had no obvious asymmetry. Conclusion: Our findings partly confirmed that use of DEX was associated with poor treatment outcome in GBM patients. To reach a definitive conclusion, large samples from multi-centers are urgent to address this concern.
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