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Restrictive Use of Dexamethasone in Glioblastoma

Restrictive Use of Dexamethasone in Glioblastoma

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04266977
Acronym
RESDEX
Enrollment
50
Registered
2020-02-12
Start date
2020-05-08
Completion date
2028-04-30
Last updated
2025-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dexamethasone, Glioblastoma, Steroids

Brief summary

The administration of steroids, most commonly dexamethasone (DEX), has established as standard of care during treatment of glioblastoma (GBM) and is widely used during the entire course of the disease including pre- and postoperative management, chemo- and radiotherapy. The primary purpose is to reduce tumor-associated vasogenic edema and to prevent or treat increased intracranial pressure. However, steroids are also linked to a multitude of adverse side effects that may affect survival of GBM patients such as major immunosuppression. The use of steroids during radiotherapy is associated with reduced overall- and progression-free survival and has been identified as an independent poor prognostic factor. Despite these findings, the suspicion of GBM often triggers the administration of DEX in routine clinical practice, regardless of neurological symptoms, tumor size, or extension of cerebral edema. The purpose of this study is to assess whether selected GBM patients can be treated safely with a restrictive DEX regimen from referral to the neurosurgical center until discharge. The primary objective is to determine the failure rate of a restrictive DEX regimen defined as edema or mass effect leading to any of the following: GCS deterioration ≥ 2 points, NIHSS increase ≥ 3 points, increase of midline Shift ≥ 2mm, or any surgical rescue procedure for increasing mass effect.

Detailed description

Background Glioblastoma (GBM) is the most common and devastating malignant brain tumor in adults. Patients with glioblastoma face a poor prognosis. Despite maximal treatment, most patients suffer tumor progression after 6-7 months and die within 1-2 years. Standard treatment for newly diagnosed glioblastoma contains maximal safe surgery and adjuvant radiochemotherapy with temozolomide. Additional administration of steroids has established as standard of care during treatment of GBM. It is widely used during the entire course of the disease including pre- and postoperative management, chemotherapy and radiotherapy. Dexamethasone (DEX) is the most frequently used steroid. The main purpose is to reduce the tumor associated vasogenic cerebral edema, to prevent or treat increased intracranial pressure. In addition, DEX helps to cope with adverse effects of GBM-treatment like nausea, vomiting and fatigue. However, steroids are also linked to a multitude of adverse side effects that may affect the survival of GBM patients such as major immunosuppression, and metabolic changes like hyperglycemia. The use of steroids during radiotherapy is associated with reduced overall- and progression-free survival and has been identified as an independent poor prognostic factor. DEX was also related to a poor prognosis in recurrent GBM. Despite these findings, in routine clinical practice, the suspicion of glioblastoma often triggers the administration of DEX, regardless of neurologic symptoms or the extension of cerebral edema. Many patients are treated with larger doses of DEX per day before being referred to a neurosurgical center and are kept on steroids during the entire treatment. On the other hand, the clinical experience shows that GBM-patients with no, or only mild neurologic symptoms, normal intracranial pressure and relatively small cerebral edema can be managed without administration of DEX. The rationale for this study is to objectify the criteria and safety of a restrictive DEX regimen (based on standardized clinical and radiological criteria). A restrictive DEX regimen may help to reduce over-use, limit the number of patients exposed to the adverse effects of DEX, and potentially improve survival in GBM-patients. The purpose of this study is to assess whether selected GBM patients can be treated safely with a restrictive DEX regimen from referral to the neurosurgical center until discharge. Objective The primary objective is to determine the failure rate of a restrictive DEX regimen defined as edema or mass effect leading to any of the following: GCS deterioration ≥ 2 points, NIHSS increase ≥ 3 points, increase of midline Shift ≥ 2mm, or any surgical rescue procedure for increasing mass effect. Methods All patients referred to the neurosurgical center with suspicion of glioblastoma are screened for inclusion- and exclusion criteria. If eligible and consenting of the patient to the study protocol, no steroids will be administered until discharge (except optional intraoperative single shot dexamethasone of max. 4mg if necessary). If steroids have been administered for a maximum of one day before referral, they will be stopped immediately. Patients are followed clinically. If one of the above-described failure criteria occurs, the primary endpoint is reached and DEX will be administered.

Interventions

DRUGDexamethasone

restrictive use of DEX, based on standardized clinical and radiological criteria.

Sponsors

Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

restrictive use of DEX, based on standardized clinical and radiological criteria.

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed supratentorial contrast enhancing lesion suspicious of glioblastoma without major mass effect, amenable to surgical resection * Age 18 - 90 years * Midline Shift ≤ 3mm * GCS ≥ 14 * NIHSS ≤ 3 * Provided written informed consent

Exclusion criteria

* Infratentorial lesions, brainstem lesions, multifocal lesions * Therapy with steroids for \>1 day before inclusion * Need for treatment with steroids due to any other disease * Contraindications to the administration of Dexamethasone * Pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Failure rate of the restrictive DEX regimen30 days after surgeryFailure rate of the restrictive DEX regimen, defined as cerebral edema or mass effect causing any of the following: GCS deterioration ≥ 2 points or NIHSS increase ≥ 3 points or Increase of midline Shift ≥ 2mm or any new herniation sign on imaging or Any surgical rescue procedure for increasing mass effect (hemicraniectomy, removal of bone flap, abortion of the procedure or emergency tumor debulking

Secondary

MeasureTime frameDescription
Cumulative dexamethasone dosage30 days after surgeryCumulative dexamethasone dosage during study period
National Institutes of Health Stroke Scale (NIHSS) over time of the study period30 days after surgeryNIHSS over time of the study period and correlation with steroid medication (Score 0-42, 0 = no deficits and 1-42 deficits)
Glasgow Coma Scale (GCS) over time of the study period and correlation with steroid medication30 days after surgeryGCS over time of the study period and correlation with steroid medication GCS over time of the study period and correlation with steroid medication (Score 15-3, 15 = patient is fully oriented, 3 = patient is intubated)
Volume of contrast enhancing tumor on preoperative MRIpresurgeryVolume of contrast enhancing tumor on preoperative MRI
Volume of contrast enhancing tumor on postoperative MRI48 hours after surgeryVolume of contrast enhancing tumor on postoperative MRI
Secondary neurological or systemic complication30 days after surgerySecondary neurological or systemic complication resulting in a 30-day morbidity or mortality
Volume of edema on postoperative MRI48 hours after surgeryVolume of edema on postoperative MRI and correlation with steroid medication
Time to start of adjuvant treatment30 days after surgeryTime to start of adjuvant treatment
Rate of reoperations30 days after surgeryRate of reoperations
Cause of reoperations30 days after surgeryCause of reoperations
Volume of edema on preoperative MRI and correlation with steroid medicationpresurgeryVolume of edema on preoperative MRI and correlation with steroid medication

Countries

Switzerland

Contacts

Primary ContactJohannes Goldberg, MD
johannes.goldberg@insel.ch+41316322409
Backup ContactNicole Söll, CDM
nicole.soell@insel.ch+41316323164

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026