Actively Recruiting
The RESBIOP-study: Resection Versus Biopsy in High-grade Glioma Patients (ENCRAM 2202)
Led by Jasper Gerritsen · Updated on 2023-11-27
564
Participants Needed
8
Research Sites
313 weeks
Total Duration
On this page
Sponsors
J
Jasper Gerritsen
Lead Sponsor
H
Haaglanden Medical Centre
Collaborating Sponsor
AI-Summary
What this Trial Is About
There are no guidelines or prospective studies defining the optimal surgical treatment for gliomas of older patients (≥70 years) or those with limited functioning performance at presentation (KPS ≤70). Therefore, the decision between resection and biopsy is varied, amongst neurosurgeons internationally and at times even within an instiutition. This study aims to compare the effects of maximal tumor resection versus tissue biopsy on survival, functional, neurological, and quality of life outcomes in these patient subgroups. Furthermore, it evaluates which modality would maximize the potential to undergo adjuvant treatment. This study is an international, multicenter, prospective, 2-arm cohort study of observational nature. Consecutive HGG patients will be treated with resection or biopsy at a 3:1 ratio. Primary endpoints are: 1) overall survival (OS) and 2) proportion of patients that have received adjuvant treatment with chemotherapy and radiotherapy. Secondary endpoints are 1) proportion of patients with NIHSS (National Institute of Health Stroke Scale) deterioration at 6 weeks, 3 months and 6 months after surgery 2) progression-free survival (PFS); 3) quality of life at 6 weeks, 3 months and 6 months after surgery and 4) frequency and severity of Serious Adverse Events (SAEs). Total duration of the study is 5 years. Patient inclusion is 4 years, follow-up is 1 year.
CONDITIONS
Official Title
The RESBIOP-study: Resection Versus Biopsy in High-grade Glioma Patients (ENCRAM 2202)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years and older and up to 90 years
- Tumor diagnosed as high-grade glioma (WHO grade III or IV) on MRI as assessed by the neurosurgeon
- Written informed consent
You will not qualify if you...
- Tumors located in the cerebellum, brainstem, or midline
- Medical reasons preventing MRI (e.g., having a pacemaker)
- Unable to provide written informed consent
- Secondary high-grade glioma from malignant transformation of low-grade glioma
- Second primary cancer within the last 5 years, except adequately treated in situ carcinoma or basal cell skin cancer
AI-Screening
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Trial Site Locations
Total: 8 locations
1
University of California, San Francisco
San Francisco, California, United States, 94143
Actively Recruiting
2
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
Actively Recruiting
3
University Hospital Leuven
Leuven, Belgium
Actively Recruiting
4
Technical University Munich
Munich, Bavaria, Germany, 74076
Not Yet Recruiting
5
University Hospital Heidelberg
Heidelberg, Germany
Actively Recruiting
6
Erasmus Medical Center
Rotterdam, South Holland, Netherlands, 3015 GD
Actively Recruiting
7
Haaglanden Medical Center
The Hague, Netherlands
Actively Recruiting
8
Inselspital Universitätsspital Bern
Bern, Switzerland, 3010
Not Yet Recruiting
Research Team
J
Jasper Gerritsen, MD PhD
CONTACT
A
Arnaud Vincent, MD PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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