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Dexamethasone and overall survival and progression free survival in patients with newly diagnosed glioblastoma: a meta-analysis.
Arora, Harshit; Mammi, Marco; Patel, Naisargi Manishkumar; Zyfi, Dea; Dasari, Hema Reddy; Yunusa, Ismael; Simjian, Thomas; Smith, Timothy R; Mekary, Rania A.
Afiliação
  • Arora H; Computational Neuroscience Outcomes Center, Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Mammi M; Neurosurgery Division, "M. Bufalini" Hospital, Cesena, Italy.
  • Patel NM; School of Pharmacy, Massachusetts College of Pharmacy and Health Sciences (MCPHS) University, Boston, MA, USA.
  • Zyfi D; School of Pharmacy, Massachusetts College of Pharmacy and Health Sciences (MCPHS) University, Boston, MA, USA.
  • Dasari HR; School of Pharmacy, Massachusetts College of Pharmacy and Health Sciences (MCPHS) University, Boston, MA, USA.
  • Yunusa I; School of Pharmacy, Massachusetts College of Pharmacy and Health Sciences (MCPHS) University, Boston, MA, USA.
  • Simjian T; College of Pharmacy, University of South Carolina, Columbia, SC, USA.
  • Smith TR; School of Pharmacy, Massachusetts College of Pharmacy and Health Sciences (MCPHS) University, Boston, MA, USA.
  • Mekary RA; Computational Neuroscience Outcomes Center, Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
J Neurooncol ; 166(1): 17-26, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38151699
ABSTRACT

PURPOSE:

Glioblastomas, the most common primary malignant brain tumors in adults, still hold poor prognosis. Corticosteroids, such as dexamethasone, are usually prescribed to reduce peritumoral edema and limit neurological symptoms, although potential detrimental effects of these drugs have been described. The present meta-analysis aimed to explore the association of dexamethasone with overall survival (OS) and progression free survival (PFS) in patients with newly diagnosed glioblastoma.

METHODS:

PubMed, Cochrane Library, Embase, and ClinicalTrials.gov were searched for pertinent studies following the Preferred Reporting Items of Systematic Review and Meta-Analysis checklist. Pooled multivariable-adjusted hazard ratios (HR) for OS and PFS and their associated 95% confidence intervals (CIs) were calculated using the random-effects model and the heterogeneity among studies was assessed using I2. The quality of evidence was assessed using the GRADE criteria.

RESULTS:

Seven studies were included, pooling data of 1,257 patients, with age varying from 11 to 81 years. Glioblastoma patients on pre- or peri-operative dexamethasone were associated with a significantly poorer overall survival (HR 1.33, 95% CI 1.15, 1.55; 7 studies; I2 59.9%) and progression free survival (HR 1.77, 95% CI 1.05, 2.97; 3 studies; I2 71.1%) compared to patients not on dexamethasone. The quality of evidence was moderate for overall survival and low for progression free survival.

CONCLUSION:

Dexamethasone appeared to be associated with poor survival outcomes of glioblastoma patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Aged / Aged80 / Child / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glioblastoma Tipo de estudo: Systematic_reviews Limite: Adolescent / Adult / Aged / Aged80 / Child / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article