Development of MRF for Characterization of Brain Tumors After Radiotherapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorCase Comprehensive Cancer Center

About this trial

The purpose of this study is to discover the potential convenience and ease of using a Magnetic Resonance Imaging (MRI) technique, named Magnetic Resonance Fingerprinting (or MRF), to achieve high-quality images within a short scan time of 5 min for viewing the entire brain. This is an advanced quantitative assessment of brain tissues. This method is being applied with IVIM MRI to be able to tell the difference between a brain with radiation necrosis and a brain with tumor recurrence. Participants will consist of individuals who have received radiation therapy in the past and were diagnosed with radiation necrosis, individuals with recurrent tumors, individuals with previously untreated tumors, and healthy individuals who have no brain diseases and have not had radiation treatment to the brain. Participants will undergo an MRI scan at a one-time research study visit; no extra tests or procedures will be required for this research study.

The primary objectives of this study are:

* To demonstrate the clinical feasibility of combining MRF with state-of-the-art parallel imaging techniques to achieve high-resolution quantitative imaging within a reasonable scan time of 5 min for whole brain coverage. * To apply the developed quantitative approach in combination with IVIM MRI for differentiation of tumor recurrence and radiation necrosis. * To investigate the effect of radiation dose on the development of radiation necrosis and tumor recurrence.

Eligibility criteria

Qualifiers

Ages 18 - 60

No history of cerebrovascular disease

No cognitive impairments

Able to provide informed consent

Disqualifiers

Pregnant women OR lactating women

Participants with ferromagnetic or otherwise non-MRI compatible aneurysm clips.

Participants who cannot go into the MRI scanner due to metal implants and other medical conditions.

The presence of an implanted medical device that is not MRI-compatible, including, but not limited to: pacemaker, defibrillator.

Trial design

Treatments tested in this trial

  • MRF in conjunction with IVIM MRI without contrast

Treatment groups

90 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Sponsors and collaborators

Case Comprehensive Cancer Center

Lead sponsor

The Cleveland Clinic

Collaborator