84 Participants Needed

Magnetic Resonance Fingerprinting for Brain Cancer

CA
Overseen ByChaitra A Badve, MD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Case Comprehensive Cancer Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

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.

Is Magnetic Resonance Fingerprinting (MRF) safe for humans?

The research on Magnetic Resonance Fingerprinting (MRF) does not specifically address safety concerns, but it has been used in various clinical applications, including brain, prostate, liver, and cardiac imaging, suggesting it is generally considered safe for human use.12345

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.14678

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.23467

Who Is on the Research Team?

CA

Chaitra A Badve, MD

Principal Investigator

University Hospitals Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center

Are You a Good Fit for This Trial?

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

I can understand and am willing to sign the consent form, or I have someone legally authorized to do so on my behalf.
I have brain metastases and can have scans at specified times after targeted brain radiation.
I have a brain tumor that was either found at the start or has shown signs of growth on scans.

Exclusion Criteria

Patients with contraindications for MRI due to embedded foreign metallic objects such as bullets, shrapnel, metalwork fragments, or other metallic material
Implanted medical device not described above that is not MRI-compatible
I am under 18 years old.
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Initial Imaging and Diagnosis

Participants undergo volumetric MRI study with contrast and 3D-MRF acquisition for surgical planning or clinical diagnosis

1-2 weeks

Treatment

Participants receive standard of care surgery, radiation, and chemotherapy

Varies based on individual treatment plans

Follow-up Imaging

Follow-up MRF scans are performed to visualize recurrence and differentiate post-treatment changes from tumor recurrence

Ongoing as determined by clinical care

Follow-up

Participants are monitored for safety and effectiveness after treatment

6 months

What Are the Treatments Tested in This Trial?

Interventions

  • Magnetic Resonance Fingerprinting
Trial Overview The study tests Magnetic Resonance Fingerprinting (MRF), an advanced MR imaging technique that quickly scans and provides detailed tissue data. This will be compared to standard imaging and clinical information to check its accuracy in diagnosing and assessing brain tumors.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Group I: Treated tumors with possible recurrenceExperimental Treatment1 Intervention
Group II: Newly Diagnosed Brain TumorsExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Case Comprehensive Cancer Center

Lead Sponsor

Trials
472
Recruited
33,400+

Published Research Related to This Trial

Magnetic Resonance Fingerprinting (MRF) is a cutting-edge imaging technique that allows for the simultaneous and efficient measurement of multiple tissue properties, which could lead to more accurate and objective diagnoses.
MRF has shown promise in various applications, including brain, prostate, liver, and cardiac imaging, as well as in assessing microvascular properties, indicating its potential to enhance patient monitoring and the development of imaging biomarkers.
Magnetic Resonance Fingerprinting-An Overview.Panda, A., Mehta, BB., Coppo, S., et al.[2020]
Magnetic Resonance Fingerprinting (MRF) demonstrated a high predictability for identifying tumor regions and grading in gliomas, achieving 88.9% accuracy for low-grade gliomas and 75% for high-grade gliomas among 17 patients studied.
While both MRF and PET imaging provide valuable quantitative data on gliomas, they reflect different biological mechanisms, indicating that they may complement each other rather than replace one another in clinical assessments.
Evaluation of Gliomas with Magnetic Resonance Fingerprinting with PET Correlation-A Comparative Study.Marik, W., Cardoso, PL., Springer, E., et al.[2023]
Magnetic resonance fingerprinting (MRF) can quickly and effectively differentiate between tumor tissue and normal white matter in pediatric brain tumor patients, with a median scan time of just 11 minutes.
MRF successfully distinguishes between low-grade and high-grade tumors based on T1 and T2 relaxation times, indicating its potential as a valuable diagnostic tool for assessing tumor characteristics in children and young adults.
Magnetic Resonance Fingerprinting to Characterize Childhood and Young Adult Brain Tumors.de Blank, P., Badve, C., Gold, DR., et al.[2020]

Citations

Magnetic Resonance Fingerprinting-An Overview. [2020]
Evaluation of Gliomas with Magnetic Resonance Fingerprinting with PET Correlation-A Comparative Study. [2023]
Magnetic Resonance Fingerprinting to Characterize Childhood and Young Adult Brain Tumors. [2020]
Magnetic resonance fingerprinting: an overview. [2021]
Magnetic Resonance Fingerprinting: A Review of Clinical Applications. [2023]
Feasibility of MR fingerprinting using a high-performance 0.55 T MRI system. [2022]
Whole-brain 3D MR fingerprinting brain imaging: clinical validation and feasibility to patients with meningioma. [2021]
Tailored magnetic resonance fingerprinting of post-operative pediatric brain tumor patients. [2023]
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