Actively Recruiting

Age: 18Years - 90Years
All Genders
NCT06146725

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

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

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

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here