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Restrictive Use of Dexamethasone in Glioblastoma (RESDEX)

Primary Purpose

Glioblastoma, Dexamethasone, Steroids

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Dexamethasone
Sponsored by
Insel Gruppe AG, University Hospital Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Kantonsspital St. Gallen
  • Universitätsspital Basel
  • Department of NeurosurgeryRecruiting
  • Universitätsspital Zürich

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment Dexamethasone

Arm Description

The restrictive DEX regimen is applied from referral to the neurosurgical center until discharge. All administered steroids will be stopped immediately after study inclusion. If one or more of the previously defined failure criteria occurs, patients will be treated with DEX.

Outcomes

Primary Outcome Measures

Failure rate of the restrictive DEX regimen
Failure 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 Outcome Measures

Secondary neurological or systemic complication
Secondary neurological or systemic complication resulting in a 30-day morbidity or mortality
Cumulative dexamethasone dosage
Cumulative dexamethasone dosage during study period
National Institutes of Health Stroke Scale (NIHSS) over time of the study period
NIHSS 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 medication
GCS 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 MRI
Volume of contrast enhancing tumor on preoperative MRI
Volume of contrast enhancing tumor on postoperative MRI
Volume of contrast enhancing tumor on postoperative MRI
Volume of edema on preoperative MRI and correlation with steroid medication
Volume of edema on preoperative MRI and correlation with steroid medication
Volume of edema on postoperative MRI
Volume of edema on postoperative MRI and correlation with steroid medication
Time to start of adjuvant treatment
Time to start of adjuvant treatment
Rate of reoperations
Rate of reoperations
Cause of reoperations
Cause of reoperations

Full Information

First Posted
February 3, 2020
Last Updated
March 22, 2023
Sponsor
Insel Gruppe AG, University Hospital Bern
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1. Study Identification

Unique Protocol Identification Number
NCT04266977
Brief Title
Restrictive Use of Dexamethasone in Glioblastoma
Acronym
RESDEX
Official Title
Restrictive Use of Dexamethasone in Glioblastoma
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 8, 2020 (Actual)
Primary Completion Date
April 2025 (Anticipated)
Study Completion Date
April 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Insel Gruppe AG, University Hospital Bern

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma, Dexamethasone, Steroids

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
restrictive use of DEX, based on standardized clinical and radiological criteria.
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment Dexamethasone
Arm Type
Experimental
Arm Description
The restrictive DEX regimen is applied from referral to the neurosurgical center until discharge. All administered steroids will be stopped immediately after study inclusion. If one or more of the previously defined failure criteria occurs, patients will be treated with DEX.
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Description
restrictive use of DEX, based on standardized clinical and radiological criteria.
Primary Outcome Measure Information:
Title
Failure rate of the restrictive DEX regimen
Description
Failure 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
Time Frame
30 days after surgery
Secondary Outcome Measure Information:
Title
Secondary neurological or systemic complication
Description
Secondary neurological or systemic complication resulting in a 30-day morbidity or mortality
Time Frame
30 days after surgery
Title
Cumulative dexamethasone dosage
Description
Cumulative dexamethasone dosage during study period
Time Frame
30 days after surgery
Title
National Institutes of Health Stroke Scale (NIHSS) over time of the study period
Description
NIHSS over time of the study period and correlation with steroid medication (Score 0-42, 0 = no deficits and 1-42 deficits)
Time Frame
30 days after surgery
Title
Glasgow Coma Scale (GCS) over time of the study period and correlation with steroid medication
Description
GCS 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)
Time Frame
30 days after surgery
Title
Volume of contrast enhancing tumor on preoperative MRI
Description
Volume of contrast enhancing tumor on preoperative MRI
Time Frame
presurgery
Title
Volume of contrast enhancing tumor on postoperative MRI
Description
Volume of contrast enhancing tumor on postoperative MRI
Time Frame
48 hours after surgery
Title
Volume of edema on preoperative MRI and correlation with steroid medication
Description
Volume of edema on preoperative MRI and correlation with steroid medication
Time Frame
presurgery
Title
Volume of edema on postoperative MRI
Description
Volume of edema on postoperative MRI and correlation with steroid medication
Time Frame
48 hours after surgery
Title
Time to start of adjuvant treatment
Description
Time to start of adjuvant treatment
Time Frame
30 days after surgery
Title
Rate of reoperations
Description
Rate of reoperations
Time Frame
30 days after surgery
Title
Cause of reoperations
Description
Cause of reoperations
Time Frame
30 days after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Johannes Goldberg, MD
Phone
+41316322409
Email
johannes.goldberg@insel.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Nicole Söll, CDM
Phone
+41316323164
Email
nicole.soell@insel.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andreas Raabe, MD
Organizational Affiliation
Inselspital Bern, Department of Neurosurgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital St. Gallen
City
Saint Gallen
State/Province
St.Gallen
ZIP/Postal Code
9007
Country
Switzerland
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marian Neidert, MD
Email
marian.neidert@kssg.ch
Facility Name
Universitätsspital Basel
City
Basel
ZIP/Postal Code
4031
Country
Switzerland
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gregor Hutter, MD
Email
Gregor.Hutter@usb.ch
Facility Name
Department of Neurosurgery
City
Bern
ZIP/Postal Code
3010
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Johannes Goldberg, MD
Phone
+41316322409
Email
johannes.goldberg@insel.ch
First Name & Middle Initial & Last Name & Degree
Nicole Söll, CDM
Phone
+41316323164
Email
nicole.soell@insel.ch
First Name & Middle Initial & Last Name & Degree
Johannes Goldberg
Facility Name
Universitätsspital Zürich
City
Zürich
ZIP/Postal Code
8091
Country
Switzerland
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vincens Kälin, MD
Email
Vincens.Kaelin@usz.ch
First Name & Middle Initial & Last Name & Degree
Carki Serra, MD
Email
Carlo.Serra@usz.ch

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
13703072
Citation
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Results Reference
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13415910
Citation
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Results Reference
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PubMed Identifier
29328002
Citation
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Results Reference
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PubMed Identifier
28138871
Citation
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Results Reference
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PubMed Identifier
27020328
Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
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Citation
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Results Reference
result

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Restrictive Use of Dexamethasone in Glioblastoma

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