Brain Imaging Biomarkers in Patients With Brain Metastasis

University Health Network, Toronto

Status and phase: Enrolling; Phase 2

Conditions: Brain Metastases, Adult

Treatments: Diagnostic Test: CT and MRI Scans

Study type: Interventional

Funder types: Other

Identifiers

NCT04197297

18-5380

Details and patient eligibility

About

A biomarker is a measurable indicator of the severity or presence of some disease state. In this study, brain metastases patients who will be receiving radiation treatment, will undergo CT (Computed Tomography) and MRI (Magnetic Resonance Imaging) scans prior to and after radiation treatment to measure these biomarkers. This is a single-center phase II study to validate the predictive abilities of biomarkers, in terms of determining how patients will respond to radiation treatment.

Full description

Advances in medical imaging can provide useful information to guide and look at the response to treatment. Previous studies suggest early changes in the tumor after radiation treatment may be detectable using special MRI (Magnetic Resonance Imaging), and CT (Computed Tomography) scans. A biomarker is a measureable indicator of the severity or presence of some disease state. Previous studies suggest that the change in several imaging biomarkers can predict who will respond to radiation treatment. In this study, patients will undergo CT and MRI scans prior to and after radiation treatment to measure these biomarkers. The purpose of this study is to validate the predictive abilities of biomarkers in terms of determining how patients will respond to radiation treatment. This is a single-center phase II study, which will be conducted at the Princess Margaret Cancer Center. The study will be enrolling up to a total of 90 patients who will be receiving radiation treatment for brain metastases. Patients will be asked to participate within this study for 2 years.

Enrollment: 90 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Biopsy proven primary malignancy (original biopsy is adequate as long as the brain imaging is consistent with brain metastases)
• At least one index lesion with diameter > 1cm and without imaging evidence of hemorrhage
• Patients age > 18 years of age
• Patients planned for RT to brain metastases
• Ability to understand and the willingness to sign a written informed consent document.

Exclusion criteria

• Previous Whole Brain Radiotherapy
• Previous radiosurgery to the index lesion
• Individuals unable to undergo contrasted MRI for whatever reason

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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90 participants in 1 patient group

CT and MRI Scans

Other group

Description:

Each patient will undergo a 3T MRI scan as well as a dynamic contrast-enhanced CT scan within one week prior to the start of treatment. Patients will also undergo a research 3T MRI scan and research dynamic contrast-enhanced CT scan at the one week post radiotherapy mark. An MRI scan during their 3 month post-treatment follow up visits will take place as per routine standard of care.

Treatment:

Diagnostic Test: CT and MRI Scans