Journal Basic Info

  • Impact Factor: 2.709**
  • H-Index: 11 
  • ISSN: 2474-1663
  • DOI: 10.25107/2474-1663
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Urological Cancers
  •  Immunology
  •  Endoscopy Methods
  •  Targeted Therapy
  •  Endometrial Cancer
  •  Kidney Cancer
  •  Palliative Care
  •  Thoracic Oncology

Abstract

Citation: Clin Oncol. 2019;4(1):1654.DOI: 10.25107/2474-1663.1654

Impact of Dexamethasone on Metabolic Profile and Survival in Glioblastoma

Yislenz Narváez-Martínez, Carme Balaña , Maria Buxó , Gemma Mateu , Alfredo Gimeno , Gerard Blasco , Josep Puig , Carme Joly-Torta , Marina Castellví-Juan , Jose Luis CaroCardera , Alejandro Ortega , Carlos Cohn and Sonia del Barco

Deparment of Neurosurgery, Hospital Universitari de Girona Doctor Josep Trueta, Spain Department of Medicine, Universitat Autònoma de Barcelona, Spain Medical Oncology Service, Catalan Institute of Oncology, Hospital Universitari Germans Trias i Pujol, Spain Girona Biomedical Research Institute (IDIBGI), Spain Department of Pathology, Hospital Universitari de Girona Doctor Josep Trueta, Spain Department of Radiology, Girona Biomedical Research Institute, Hospital Universitari de Girona Doctor Josep Trueta, Spain Medical Oncology Service, Catalan Institute of Oncology, Hospital Universitari de Girona Doctor Josep Trueta, Spain

*Correspondance to: Yislenz Narváez-Martínez 

 PDF  Full Text Research Article | Open Access

Abstract:

Background: Although patients with glioblastoma require corticosteroids, such as dexamethasone, for symptom control, they could worsen prognosis. However, it is not clear whether personalized corticosteroid doses have this effect. We have examined the effects of different doses of dexamethasone on the metabolic profile and prognosis of patients with glioblastoma. Methods: Patients diagnosed with glioblastoma from 2013 to 2016 were included. We recorded changes in glycemia, glycosylated hemoglobin, insulin, Insulin-like Growth Factor 1 (IGF1), triglycerides, and total cholesterol and correlated these changes with dexamethasone dose, Progression-Free Survival (PFS), and Overall Survival (OS). Results: Among the 32 evaluable patients, the median daily dose of dexamethasone during radiotherapy and concomitant temozolomide was 1.4 mg/day (range=0, 8.3 mg/day). The median cumulative dose of dexamethasone was 250 mg (range=0 to 2,648 mg). Neither dexamethasone during concomitant therapy nor median cumulative dose >250 mg was associated with PFS or OS. Total cholesterol increase at progression relative to baseline levels (+20.5 mg/dL, p=0.04) was associated with cumulative dexamethasone dose >250 mg (p=0.01). Only hyperglycemia was identified as an independent marker of shorter PFS (HR, 3.7; 95% CI=1.3, 10.8; p=0.02) and OS (HR, 8.4; 95% CI=2.6, 27.1; p<0.001). Conclusion: Personalized doses of dexamethasone are not associated with worse outcome. The interrelation between dexamethasone, cholesterol, and outcome merits further investigation.

Keywords:

Dexamethasone; Glioblastoma; Glycemic profile; Lipid profile; Survival

Cite the Article:

Narváez-Martínez Y, Balaña C, Buxó M, Mateu G, Gimeno A, Blasco G, et al. Impact of Dexamethasone on Metabolic Profile and Survival in Glioblastoma. Clin Oncol. 2019;4:1654.

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