Recruiting

Observational Study

Sponsor:

Jonsson Comprehensive Cancer Center

Code:

NCT06090903

Conditions

Glioblastoma

Recurrent Glioblastoma

Resectable Glioblastoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Biospecimen Collection

Magnetic Resonance Imaging

Medical Chart Review

Study Details

Brief summary:

This clinical trial uses a type of imaging scan called magnetic resonance imaging (MRI) to study brain tumor biology in patients with glioblastoma that can be removed by surgery (resectable). Malignant gliomas are the second leading cause of cancer mortality in people under the age of 35 in the United States. Glioblastoma is a type of malignant glioma with very poor patient prognosis. There are currently only about 3 drugs approved by the Food and Drug Administration (FDA) for the treatment of glioblastoma, one of them being administration of bevacizumab, which is very expensive. It is the most widely used treatment for glioblastoma with dramatic results. However, previous clinical trials have not demonstrated an overall survival benefit across all patient populations with glioblastoma that has returned after treatment (recurrent). The study aims to identify which patients who will benefit from bevacizumab therapy by observing MRI images and corresponding imaging biomarkers.

Conditions

Glioblastoma

Recurrent Glioblastoma

Resectable Glioblastoma

Study ID

NCT06090903

Start date

Apr 14, 2022

Status verified date

Nov, 2025

Completion date

Apr 18, 2028

Anticipated

Primary completion date

Apr 18, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Patients > 18 years of age
  • Patients with newly diagnosed, suspected or recurrent glioblastoma (GBM) patients with enhancing tumors greater than 1.5 mL clinically indicated for surgical resection. Recurrent GBM must have occurred more than 3 months after the end of radiation therapy per Response Assessment in Neuro-Oncology Criteria (RANO) guidelines

Exclusion Criteria:

  • Counterindication to magnetic resonance imaging (MRI) (Patient has a pacemaker or metal in the body)
  • Patients < 18 years of age

Study Design

Enrollment

50 participants

Anticipated

Intervention Model

Single group

Primary purpose

Screening

Interventions and Outcome Measures

Arms

experimental: Screening (MRI)

Patients undergo one MRI scan over approximately 1 hour prior to surgery.

Interventions

Biospecimen Collection

patients will receive 1-3 image-guided biopsies within tumor tissue already designated for resection or removal.

Magnetic Resonance Imaging

Undergo MRI scan

Medical Chart Review

Review Medical Chart

Primary outcome measure

  • Decorin (DCN) expression [ Time Frame: Up to 5 years ]
  • DCN expression correlated to ADCL [ Time Frame: Up to 5 years ]
  • Incidence of tumors with high diffusion measurements among MES-like cells [ Time Frame: Up to 5 years ]
  • DCN expression among Mesenchymal-Like (MES-like) cells [ Time Frame: Up to 5 years ]

Central Contacts and Locations

Locations

UCLA / Jonsson Comprehensive Cancer Center

Recruiting

Los Angeles, California, United States, 90095

Contacts

Principal Investigator:

Benjamin M. Ellingson

More Information

Sponsor

Jonsson Comprehensive Cancer Center

Last update posted

Nov 10, 2025

Last verified

Nov, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Jonsson Comprehensive Cancer Center on 2025-11-10.