RecruitingNCT06146725

The RESBIOP-study: Resection Versus Biopsy in High-grade Glioma Patients (ENCRAM 2202)


Sponsor

Jasper Gerritsen

Enrollment

564 participants

Start Date

Jan 1, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 90 Years

Plain Language Summary

Simplified for easier understanding

This study compares two surgical approaches for people newly diagnosed with a high-grade brain tumor (glioma): removing as much of the tumor as possible (resection) versus taking just a small tissue sample (biopsy). The goal is to better understand which approach is more beneficial and when. **You may be eligible if...** - You are between 18 and 90 years old - An MRI scan shows a suspected high-grade glioma (grade III or IV brain tumor, including glioblastoma) - A neurosurgeon has reviewed your case - You are able to give written informed consent **You may NOT be eligible if...** - Your tumor is located in the cerebellum, brain stem, or midline structures - You cannot have an MRI (e.g., pacemaker) - You are unable to give written consent - Your high-grade glioma grew from a previously known lower-grade glioma - You have had another cancer in the past 5 years (except minor skin cancers or in-situ cancers) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURETumor resection

Maximal safe resection of the tumor

PROCEDURETumor biopsy

Biopsy of the tumor


Locations(8)

University of California, San Francisco

San Francisco, California, United States

Massachusetts General Hospital

Boston, Massachusetts, United States

University Hospital Leuven

Leuven, Belgium

Technical University Munich

Munich, Bavaria, Germany

University Hospital Heidelberg

Heidelberg, Germany

Erasmus Medical Center

Rotterdam, South Holland, Netherlands

Haaglanden Medical Center

The Hague, Netherlands

Inselspital Universitätsspital Bern

Bern, Switzerland

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NCT06146725


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