Overview
This clinical trial studies the use of 7-Tesla (7T) magnetic resonance imaging (MRI) in detecting melanoma that has spread to the brain (melanoma brain metastases). The standard MRI brain imaging is done on 3T or similar MRI machine, but the 7T MRI machine has a larger magnet which has been shown to have superior resolution of the brain and of non-cancerous brain lesions. Diagnostic procedures such as 7T MRI may help find and diagnose melanoma brain metastases earlier than standard 3T MRI.
Description
PRIMARY OBJECTIVE:
I. Assess the potential superiority of contrast-enhanced (CE) 7T MRI by comparing to standard of care CE 3T MRI in detecting occult brain metastases lesion at time of diagnosis of new brain metastases.
SECONDARY OBJECTIVE:
I. Describe the imaging characteristics of melanoma brain metastases on 7T MRI of the brain.
EXPLORATORY OBJECTIVE:
I. Evaluate incidence of diagnosis of leptomeningeal disease on CE 7T MRI brain.
- OUTLINE
Within 2 weeks of initial standard of care 3T MRI, patients undergo 7T MRI scan with and without contrast over 1-2 hours.
Eligibility
Inclusion Criteria:
- Melanoma patients with new untreated brain metastases seen on CE 3T MRI
- Patient may have received previous systemic therapy, immunotherapy, or checkpoint inhibitors
- Patient may have previous brain metastases treated >30 days prior with brain radiation, either whole brain radiation or radiosurgery
- Age >= 18 years
- Karnofsky performance status (KPS) >= 70
- Women of child-bearing potential and men must agree to use adequate contraception
(hormonal or barrier method of birth control; abstinence) prior to study entry, for
the duration of study participation, and for 90 days following completion of therapy.
Should a woman become pregnant or suspect she is pregnant while participating in this
study, she should inform her treating physician immediately. Women of child-bearing
potential need negative urine human chorionic gonadotropin (hCG) within 2 weeks prior
to any treatment. A female of child-bearing potential is defined as any woman
(regardless of sexual orientation, having undergone a tubal ligation, or remaining
celibate by choice) who meets the following criteria:
- Has not undergone a hysterectomy or bilateral oophorectomy; or
- Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months)
- Ability to tolerate MRI (able to lie flat in supine position without undue anxiety or
discomfort or history of claustrophobia)
- Ability to understand and the willingness to sign a written informed consent
Exclusion Criteria:
- 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 who have had central nervous system (CNS)-directed radiotherapy =< 30 days prior to entering the study or those who have not recovered from adverse events due to agents administered more than 30 days earlier
- 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
- Patients with MRI-incompatible pacemakers or MRI-incompatible implants
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to gadolinium-based contrast agents (GBCA) or other agents used in study
- Patients with poor renal function (estimated glomerular filtration rate [eGFR] < 30) or requiring dialysis
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- Patients must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants