Magnetic Resonance Fingerprinting for Brain Cancer
Trial Summary
What is the purpose of this trial?
The purpose of the research study is to test new methods that could improve diagnosis and assessment of brain tumors. One of these methods is a new MR (magnetic resonance) imaging technique called magnetic resonance fingerprinting (MRF), which allows for rapidly scanning the patient and provides quantitative information on tumor tissue. The investigators will compare the data gathered from MR Fingerprinting with other imaging tests, clinical information, treatment details and biopsy results to evaluate the accuracy of this new technique.
Do I need to stop my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What data supports the effectiveness of the treatment Magnetic Resonance Fingerprinting for brain cancer?
Magnetic Resonance Fingerprinting (MRF) is a promising tool for diagnosing brain tumors by providing detailed maps of tissue properties, which can help distinguish between tumor and normal brain tissue. It has been used in various clinical applications, including brain tumor characterization, and shows potential in predicting tumor regions and grading when combined with other imaging techniques like PET.12345
Is Magnetic Resonance Fingerprinting (MRF) safe for humans?
How is Magnetic Resonance Fingerprinting different from other brain cancer treatments?
Magnetic Resonance Fingerprinting (MRF) is unique because it provides rapid, simultaneous mapping of multiple tissue properties, like T1 and T2 relaxation times, which helps in distinguishing tumor characteristics and grades. Unlike traditional imaging, MRF offers a quantitative approach, potentially improving diagnosis and treatment planning for brain cancer.23468
Research Team
Chaitra A Badve, MD
Principal Investigator
University Hospitals Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center
Eligibility Criteria
This trial is for adults with a new or previously treated brain tumor who can give informed consent themselves or through a legal representative. It's not for those with non-MRI safe implants, metallic foreign objects in their body, severe claustrophobia, pregnant women, prisoners, vulnerable populations, non-English speakers, or minors.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Initial Imaging and Diagnosis
Participants undergo volumetric MRI study with contrast and 3D-MRF acquisition for surgical planning or clinical diagnosis
Treatment
Participants receive standard of care surgery, radiation, and chemotherapy
Follow-up Imaging
Follow-up MRF scans are performed to visualize recurrence and differentiate post-treatment changes from tumor recurrence
Follow-up
Participants are monitored for safety and effectiveness after treatment
Treatment Details
Interventions
- Magnetic Resonance Fingerprinting
Find a Clinic Near You
Who Is Running the Clinical Trial?
Case Comprehensive Cancer Center
Lead Sponsor