Recruiting

Resection vs. Biopsy

Sponsor:

Jasper Gerritsen

Code:

NCT06146725

Conditions

Glioblastoma

Glioblastoma, IDH-wildtype

Glioblastoma Multiforme

Glioblastoma Multiforme, Adult

Glioblastoma Multiforme of Brain

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Tumor resection

Tumor biopsy

Study Details

Brief 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.

Conditions

Glioblastoma

Glioblastoma, IDH-wildtype

Glioblastoma Multiforme

Glioblastoma Multiforme, Adult

Glioblastoma Multiforme of Brain

Study ID

NCT06146725

Start date

Jan 1, 2023

Status verified date

Nov, 2023

Completion date

Jan 1, 2029

Anticipated

Primary completion date

Jan 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Age ≥18 years and ≤90 years
2. Tumor diagnosed as HGG (WHO grade III/IV) on MRI as assessed by the neurosurgeon
3. Written informed consent

Exclusion Criteria:

1. Tumors of the cerebellum, brainstem or midline
2. Medical reasons precluding MRI (e.g. pacemaker)
3. Inability to give written informed consent
4. Secondary high-grade glioma due to malignant transformation from low-grade glioma
5. Second primary malignancy within the past 5 years with the exception of adequately treated in situ carcinoma of any organ or basal cell carcinoma of the skin

Study Design

Enrollment

564 participants

Anticipated

Interventions and Outcome Measures

Arms

Tumor resection

Tumor resection

Tumor biopsy

Tumor biopsy

Interventions

Tumor resection

Maximal safe resection of the tumor

Tumor biopsy

Biopsy of the tumor

Primary outcome measure

  • Overall survival [ Time Frame: Up to 5 years postoperatively ]
  • Adjuvant treatment with chemotherapy and radiotherapy [ Time Frame: 6 months postoperatively ]

Central Contacts and Locations

Central contacts

Locations

University of California, San Francisco

Recruiting

San Francisco, California, United States, 94143

Massachusetts General Hospital

Recruiting

Boston, Massachusetts, United States, 02114

More Information

Sponsor

Jasper Gerritsen

Last update posted

Nov 27, 2023

Last verified

Nov, 2023

Keywords

  • Resection
  • Biopsy
  • Survival
  • Quality of life

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Jasper Gerritsen on 2023-11-27.