Actively Recruiting
Impact of Reducing the Irradiation Volume on Survival, Toxicity, and Quality of Life in Patients With Glioblastoma Treated With Radiochemotherapy: a Prospective Multicenter Randomised Study
Led by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Updated on 2026-02-27
347
Participants Needed
23
Research Sites
N/A
Total Duration
On this page
Sponsors
C
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead Sponsor
B
Belgium Health Care Knowledge Centre
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating a new approach to radiotherapy for patients with glioblastoma, a common and aggressive brain tumor. This trial aims to determine if focusing radiation treatment more precisely by reducing the usual safety margin can safely decrease side effects and improve quality of life. Despite current treatments involving surgery, radiotherapy, and chemotherapy, survival remains limited and quality of life is often impaired for these patients. The study compares two radiotherapy approaches: one with the standard irradiation volume including a 15mm safety margin around the tumor, and another with a reduced 10mm margin to limit the amount of healthy brain tissue exposed. Both groups receive chemoradiotherapy as part of their treatment. This national multicenter trial will randomize patients to either the standard or reduced radiotherapy volume to assess outcomes. Participants will be followed for up to two years with regular assessments of overall survival, neurocognitive function, treatment-related toxicity, quality of life, disease progression, and recurrence patterns. Evaluations include baseline measurements and follow-ups at one month and one year after radiotherapy. Researchers will also monitor use of anti-edema therapy during the study. The total participation duration and study procedures are designed to monitor safety and the impact of the radiation volume on patient well-being.
CONDITIONS
Brief Title
Achieving a Better Outcome Through Limiting the Glioblastoma Clinical Target Volume
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants capable of giving informed consent
- Age >= 18 years
- WHO performance status 0-2
- Newly diagnosed glioblastoma confirmed by biopsy or resection
- Indication for chemoradiotherapy confirmed by multidisciplinary tumour board
You will not qualify if you...
- Participation in a competing trial
- Known contraindication to undergo MRI scans
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - During radiochemotherapy treatment period
Participants receive radiotherapy with either a reduced irradiation volume (CTV=10mm) or standard irradiation volume (CTV=15mm) along with chemoradiotherapy.
Duration - Up to 2 years after treatment
Participants are monitored for survival, neurocognitive functioning, radiation-induced toxicity, health-related quality of life, progression-free survival, pattern of recurrence, and anti-edema therapy effects.
Assessments at baseline, 1 month after radiotherapy, and at 1 year; ongoing monitoring until 2 years
Trial Site Locations
Total: 23 locations
1
Olv Azorg
Aalst, Belgium, 9300
Not Yet Recruiting
2
EpiCURA
Baudour, Belgium, 7331
Actively Recruiting
3
AZ Sint Jan
Bruges, Belgium, 8000
Actively Recruiting
4
Institut Jules Bordet
Brussels, Belgium, 1070
Not Yet Recruiting
5
UZ Brussel
Brussels, Belgium, 1090
Not Yet Recruiting
6
Cliniques universitaires Saint-Luc
Brussels, Belgium, 1200
Actively Recruiting
7
Ziekenhuis Oost-Limburg (ZOL)
Genk, Belgium, 3600
Actively Recruiting
8
AZ Sint-Lucas
Ghent, Belgium, 9000
Actively Recruiting
9
UZ Gent
Ghent, Belgium, 9000
Not Yet Recruiting
10
Grand Hôpital de Charleroi
Gilly, Belgium, 6060
Actively Recruiting
11
JESSA Ziekenhuis
Hasselt, Belgium, 3500
Actively Recruiting
12
AZ Groeninge
Kortrijk, Belgium, 8500
Actively Recruiting
13
Chu Helora
La Louvière, Belgium, 7100
Actively Recruiting
14
UZ Leuven
Leuven, Belgium, 3000
Actively Recruiting
15
CHU Liège
Liège, Belgium, 4000
Actively Recruiting
16
AZ Sint Maarten
Mechelen, Belgium, 2800
Actively Recruiting
17
Hôpital André Vésale - HUmani
Montigny-le-Tilleul, Belgium, 6110
Actively Recruiting
18
CH Mouscron
Mouscron, Belgium, 7700
Not Yet Recruiting
19
CHU UCL Namur - Sainte Elisabeth
Namur, Belgium, 5000
Actively Recruiting
20
AZ Delta
Roeselare, Belgium, 8800
Actively Recruiting
21
Cliniques de l'Europe
Uccle, Belgium, 1180
Actively Recruiting
22
CHR Verviers
Verviers, Belgium, 4800
Actively Recruiting
23
ZAS Augustinus
Wilrijk, Belgium, 2610
Actively Recruiting
Research Team
D
Dario Di Perri, MD
C
Chloë De Laet
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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