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7T MRI Scan for Detecting Melanoma Brain Tumors
N/A
Recruiting
Led By Lindsay Hwang
Research Sponsored by University of Southern California
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Karnofsky performance status (KPS) >= 70
Melanoma patients with new untreated brain metastases seen on CE 3T MRI
Must not have
Patients who have had brain neurosurgery =< 30 days prior to entering the study or those who have not recovered from adverse events related to that procedure
Patients with claustrophobia or anxiety limiting ability to tolerate MRI scans. Unable to tolerate MRI scan without use of anxiolytic medication or with distress requiring termination of scan or resulting in scans of poor quality
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at baseline
Awards & highlights
No Placebo-Only Group
Summary
This trial studies using a special MRI machine with a stronger magnet to take clearer pictures of the brain in patients whose melanoma has spread there. The goal is to see if this new MRI can find cancer better than the standard MRI.
Who is the study for?
This trial is for adults with melanoma that may have spread to the brain. Participants must be able to undergo MRI scans without distress, have a performance status indicating they can carry out daily activities, and agree to use contraception. It's not suitable for those with poor kidney function, recent neurosurgery or radiotherapy, uncontrolled illnesses, claustrophobia severe enough to prevent MRI scans, incompatible implants, or allergies to contrast agents used in MRIs.
What is being tested?
The study is testing whether a high-resolution 7 Tesla (7T) MRI scan can detect brain metastases from melanoma more effectively than the standard 3 Tesla (3T) MRI scan. The goal is early detection of cancer spread which could lead to better treatment outcomes.
What are the potential side effects?
While there are typically no side effects associated with undergoing an MRI scan itself, some individuals might experience discomfort lying still during the procedure or anxiety due to the enclosed space of the scanner. There's also a small risk of allergic reaction to gadolinium-based contrast agents used during imaging.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am able to care for myself but may not be able to do active work.
Select...
I have melanoma with new brain metastases not yet treated.
Select...
I am 18 years old or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I had brain surgery more than 30 days ago or have recovered from it.
Select...
I cannot undergo MRI scans due to severe claustrophobia or anxiety.
Select...
My kidney function is very low or I am on dialysis.
Select...
I do not have any serious illnesses or social situations that would stop me from following the study's requirements.
Select...
I haven't had brain-directed radiotherapy in the last 30 days or recovered from its side effects.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 14 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 14 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Presence or absence of brain metastases on 7 tesla (T) magnetic resonance imaging (MRI) as compared to the standard of care 3T MRI
Primary tumor size
Other study objectives
Incidence of diagnosis of leptomeningeal disease on CE 7T MRI brain
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Diagnostic (7T MRI)Experimental Treatment1 Intervention
Within 2 weeks of initial standard of care 3T MRI, patients undergo 7T MRI scan with and without contrast over 1-2 hours.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for melanoma include surgical resection, stereotactic radiosurgery (SRS), whole-brain radiation therapy (WBRT), immunotherapy, and targeted therapy. Surgical resection involves physically removing the tumor, which is most effective when the melanoma is detected early.
SRS delivers precise, high-dose radiation to the tumor, minimizing damage to surrounding brain tissue, and is often used for limited brain metastases. WBRT is used for multiple brain metastases, providing a broader treatment area but with more side effects.
Immunotherapy, such as checkpoint inhibitors, boosts the body's immune system to recognize and attack melanoma cells. Targeted therapy involves drugs that specifically target genetic mutations in melanoma cells, such as BRAF inhibitors.
Early detection of brain metastases using advanced imaging like 7T MRI can significantly impact treatment decisions, potentially leading to more effective and less invasive interventions.
Find a Location
Who is running the clinical trial?
University of Southern CaliforniaLead Sponsor
944 Previous Clinical Trials
1,604,620 Total Patients Enrolled
National Cancer Institute (NCI)NIH
13,917 Previous Clinical Trials
41,014,440 Total Patients Enrolled
Lindsay HwangPrincipal InvestigatorUniversity of Southern California
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am able to care for myself but may not be able to do active work.I have melanoma with new brain metastases not yet treated.I had brain radiation for metastases more than 30 days ago.I agree to use birth control during and 90 days after the study, and I am not pregnant.I had brain surgery more than 30 days ago or have recovered from it.You have had allergic reactions to similar substances as the contrast agent used in the study.I cannot undergo MRI scans due to severe claustrophobia or anxiety.I am 18 years old or older.You can stay still and calm during an MRI scan without feeling anxious or uncomfortable.My kidney function is very low or I am on dialysis.I do not have any serious illnesses or social situations that would stop me from following the study's requirements.I haven't had brain-directed radiotherapy in the last 30 days or recovered from its side effects.I have had treatments like chemotherapy or immunotherapy before.
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Research Study Groups:
This trial has the following groups:- Group 1: Diagnostic (7T MRI)
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