Actively Recruiting
Advanced Dual-Nuclei MRI to Differentiate Recurrent Brain Metastases and Radiation Necrosis
Led by Jonsson Comprehensive Cancer Center · Updated on 2026-01-15
42
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
J
Jonsson Comprehensive Cancer Center
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating advanced magnetic resonance imaging (MRI) techniques, including diffusion-relaxation correlation spectrum imaging (DR-CSI) and sodium imaging, to distinguish between recurrent brain tumors and radiation-related tissue damage called radiation necrosis (RN). These conditions often look similar on standard MRI scans, making it difficult for doctors to decide the best treatment approach. This study aims to develop new imaging methods to improve diagnosis and predict treatment outcomes in patients with metastatic brain tumors. The study has two parts. In the first, patients scheduled for surgical removal or biopsy of brain tumors undergo advanced DR-CSI and sodium MRI scans lasting about 30 minutes before their standard care. Tissue samples are also collected for analysis. In the second part, patients scheduled for stereotactic radiosurgery (SRS) receive the same advanced MRI scans before treatment and then again at 2 weeks, 3 months, and 6 months after SRS. Clinical MRIs accompany both parts to track changes over time. Participants will undergo multiple imaging sessions and, for some, tissue sampling. The study measures imaging features of recurrent brain metastases and radiation necrosis, correlates imaging with tissue analysis, and monitors early imaging changes to predict clinical outcomes. These assessments occur before surgery or biopsy in the first part and at specified intervals after SRS in the second. The total involvement duration varies depending on the assigned part of the study, with close monitoring throughout.
CONDITIONS
Brief Title
Advanced Magnetic Resonance Imaging for the Identification of Recurrent Brain Tumors and Radiation Necrosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years old
- Diagnosed with metastatic brain tumor
- Scheduled for surgical resection or tissue biopsy with or without laser interstitial thermal therapy (LITT) (Aim 1)
- Scheduled for stereotactic radiosurgery (SRS) treatment (Aim 2)
You will not qualify if you...
- Contraindications to MRI or severe kidney impairment
- Evidence of widespread leptomeningeal disease
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to the time of surgery or biopsy for Aim 1; baseline period before stereotactic radiosurgery for Aim 2
Participants undergo advanced dual-nuclei MRI and clinical MRI to differentiate recurrent brain metastases and radiation necrosis. Tissue samples are collected for those undergoing surgical resection or biopsy.
1 visit prior to surgical resection or biopsy for Aim 1; 1 visit prior to stereotactic radiosurgery for Aim 2
Duration - 6 months
Participants in Aim 2 undergo follow-up advanced MRI and clinical MRI to monitor microstructural changes after stereotactic radiosurgery and predict clinical outcomes.
3 visits at 2 weeks, 3 months, and 6 months post-stereotactic radiosurgery
Trial Site Locations
Total: 1 location
1
UCLA / Jonsson Comprehensive Cancer Center
Los Angeles, California, United States, 90095
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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