Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT05641220

Biopsy Versus Resection in Elderly Glioblastoma Patients. A Prospective Cohort Study.

This trial is set up as a prospective observational cohort study to identify if either biopsy or resection should be the surgical modality of choice in elderly glioblastoma patients with a newly diagnosed tumor. Patients who are considered eligible for GBM resection or biopsy will be included. Through shared-decision making patients and their treating physicians will decide upon resection or biopsy. Written informed consent will be obtained. Participants will be followed for 1 year postoperative to assess potential differences in health-related quality of life and overall survival.

Follow-up will consist of health-related quality of life questionaires and neurological assessment at 6 weeks, 3 months, 6 months and 12 months postoperative. Additionally Cognitive and neuro-linguistic tests will be done at 3 months postoperative. These will be compared to results pre-operative.

After surgery, patients will receive standard adjuvant treatment with concomitant Temozolomide and radiation therapy, and standard follow-up. Patients in whom the diagnosis GBM is not confirmed in histological analyses will be excluded from the study. Total study duration will be 4 years, of which 3 years will comprise patient inclusion, with a follow-up duration of 1 year.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Conditions

Glioblastoma Astrocytoma Glioma Neoplasms Neoplasms by Histologic Type Neoplasms, Germ Cell and Embryonal Neoplasms, Glandular and Epithelial Neoplasms, Nerve Tissue Neoplasms, Neuroepithelial Neuroectodermal Tumors

Age range

70 year–95 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Northwest Clinics, Alkmaar, Netherlands

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥70 years
  • Tumor diagnosed as glioblastoma on MRI with distinct ring-like pattern of contrast enhancement with thick irregular walls and a core area reduced signal suggestive of tumor necrosis as assessed by the surgeon.
  • Karnofsky Performance Score (KPS) ≥70
  • Written Informed consent

Exclusion criteria

  • Tumors of the cerebellum, brain stem or midline
  • Multifocal contrast enhancing lesions
  • Substantial non-contrast enhancing tumor areas suggesting low grade gliomas with malignant transformation
  • Medical reasons precluding MRI (e.g. pacemaker)
  • Inability to give consent as assessed by neurosurgeon (e.g. language barrier)
  • Severe aphasia prohibiting neurolinguistic testing and comprehension of informed consent
  • Previous brain tumor surgery
  • Previous low-grade glioma
  • 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.

Treatment and study plan

Primary outcomes

  1. Overall survival (OS)

    Time frame: 12 months

    Defined as the time from diagnosis to the death of the patient from any cause

  2. The difference in mean change score of physical functioning, as measured with the EORTC QLQ-C30 physical functioning scale, between the two groups at 6 weeks and 3 months after surgery compared to mean score on baseline

    Time frame: 6 weeks and 3 months after surgery

    Measured with the European Organisation for Research and Treatment of Cancer Core Quality of Life questionnaire (EORTC QLQ-C30), a higher scores means a worse outcome. We assume a minimally important difference of 7 between the 2 groups.

Secondary outcomes

  1. Progression-free survival (PFS), defined as the time from diagnosis to disease progression

    Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months after surgery

    Increase in residual tumor volume of more than 25%, or occurrence of a new tumor lesion with a volume greater than 0.175cm3), or death. As according to the RANO criteria.

  2. The difference in mean change score of physical functioning, as measured with the EORTC QLQ-C30 physical functioning scale, between the two groups at 6 months and 12 months after surgery compared to mean score on baseline.

    Time frame: at 6 months and 12 months after surgery

    Measured with the European Organisation for Research and Treatment of Cancer Core Quality of Life questionnaire (EORTC QLQ-C30), a higher scores means a worse outcome.

  3. The proportion of patients with deterioration, improvement or stable physical functioning, as measured with the EORTC QLQ-C30 physical functioning scale at 6 weeks and 3 months compared to baseline.

    Time frame: 6 weeks and 3 months after surgery

    Measured with the European Organisation for Research and Treatment of Cancer Core Quality of Life questionnaire (EORTC QLQ-C30), a higher scores means a worse outcome.

  4. Descriptive reporting of changes in the mean scores on the other health-related quality of life (HRQoL) scales at 6 weeks and 3 months after surgery.

    Time frame: at 6 weeks and 3 months postoperative

    HRQoL will be measured using the Measured with the European Organisation for Research and Treatment of Cancer (EORTC) Core Quality of Life questionnaire (QLQ-C30), EORTC , EORTC brain cancer module (QLQ-BN20) and EuroQol 5 Dimensions (EQ-5D) questionnaires. A higher scores means a worse outcome.

  5. Proportion of patients with NIHSS (National Institute of Health Stroke Scale) deterioration, improvement or stability at 6 weeks and 3 months after surgery

    Time frame: at 6 weeks and 3 months postoperative

    In which deterioration is defined as an increase of at least one point and improvement as a decrease of at least one point on the total NIHSS score compared to this score at baseline.

  6. Descriptive reporting of differences between the groups in cognitive and neuro-linguistic screening at 3 months compared to baseline.

    Time frame: 3 months postoperative

    as measured by the Aphasia Bedside Check (ABC), Shortened Token Test, verbal fluency (category and letter), Montreal Cognitive Assessment (MOCA) and optionally CAT-NL Picture Description and Object Naming.

  7. Comparison of the (S)AEs in both groups.

    Time frame: 6 weeks postoperative

  8. Cost-effectiveness between the two treatments.

    Time frame: 12 months postoperative

    Measured as total intramural medical costs, for a 1 year time horizon

Study contacts

Contact information is provided by the study sponsor or research team.

Arnaud J.P.E. Vincent, Prof. Dr.

CONTACT

[email protected]

Yvette de Haan, drs

CONTACT

[email protected]

+31612594000

Sponsors and collaborators

Lead sponsor

Erasmus Medical Center

Other

Registry information

Acronym: BIOPSY

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Dec 7, 2022
Registry last updated
Dec 7, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.