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Quantitative MRI in Assessing Disease in Patients With Brain Tumors

Quantitative High-Field Magnetic Resonance Imaging (MRI) for Assessing Brain Metastases

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02269111
Enrollment
10
Registered
2014-10-20
Start date
2015-04-30
Completion date
2018-05-31
Last updated
2018-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tumors Metastatic to Brain, Unspecified Adult Solid Tumor, Protocol Specific

Brief summary

This pilot clinical trial studies quantitative magnetic resonance imaging (MRI) at 3 Tesla in assessing disease in patients with tumors that have spread to the brain (brain metastases). In addition to routine care brain imaging of the brain, this study will include advanced multiparametric MRI sequences to measure vascular, cellular, and molecular properties of the tumor. Performing extra scans during MRI provides more information about the metastases and may better predict treatment response.

Detailed description

PRIMARY OBJECTIVES: I. To correlate pre-treatment measures of biophysical parameters in metastases-obtained using advanced, quantitative MRI techniques in patients receiving standard-of-care (SOC) therapy for 1-4 brain metastases-with treatment-induced changes in lesion size, time-to-progression (TTP), and overall survival (OS). OUTLINE: Patients undergo hybrid 3 Tesla MRI examination that includes standard MRI sequences, diffusion-weighted (DW)-MRI, chemical exchange saturation transfer (CEST), and combined dynamic contrast enhanced (DCE)-MRI/dynamic susceptibility contrast (DSC)-MRI at baseline.

Interventions

PROCEDUREdiffusion-weighted magnetic resonance imaging

Undergo DW-MRI

PROCEDUREdynamic contrast-enhanced magnetic resonance imaging

Undergo DCE-MRI

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Vanderbilt-Ingram Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients must sign an Institutional Review Board (IRB)-approved informed consent document * Patients must have been diagnosed with one of the following: * Primary brain tumor (glioma, GBM etc); or * Up to 10 brain metastases * Patients must have been diagnosed with 1-4 brain metastases * At least one of the brain metastases must measure 5 mm (or more) in short axis diameter in the axial plane * Patients must be scheduled to undergo standard brain cancer interventions: * Chemotherapy or targeted antiangiogenic therapy, in the case of primary brain tumor; or * Stereotaxic radiotherapy (SRS) or whole brain radiotherapy (WBRT), in the case of brain metastases. * Patients must be scheduled to receive a 3-Tesla (3T) MRI exam as part of their standard of care (this exam will be modified to also include pulse sequences with are for research only)

Exclusion criteria

* Patients who have received previous treatment (chemotherapy or radiotherapy) for any brain tumor (primary or metastatic). * Patients who are scheduled to receive a 1.5T MRI exam * Patients incapable of giving informed written consent, due to mental disability, altered mental status, confusion, cognitive impairment, or psychiatric disorders. * Patients scoring 14.5 or lower on the University of California, San Diego Brief Assessment of Capacity to Consent (UBACC) questionnaire will not be allowed on the study

Design outcomes

Primary

MeasureTime frameDescription
Volume transfer constant (Ktrans), as measured by DCE-MRIBaselineThe ability of pre-treatment estimates of Ktrans to predict objective tumor response by Response Evaluation Criteria in Solid Tumors or Macdonald criteria after therapy will be assessed using the proportional odds model.

Secondary

MeasureTime frameDescription
Apparent diffusion coefficient (ADC), as measured by DW-MRIBaselineCox proportional hazards regression will be used to assess the association of ADC with change in tumor size.
Extravascular extracellular volume fraction (Ve), as measured by DCE-MRIBaselineCox proportional hazards regression will be used to assess the association of Ve with change in tumor size.
Plasma volume fraction (Vp), as measured by DCE-MRIBaselineCox proportional hazards regression will be used to assess the association of Vp with change in tumor size.
Amide proton transfer asymmetry (APTasym) as measured by CESTBaselineCox proportional hazards regression will be used to assess the association of APTasym with change in tumor size.
Cerebral blood flow (CBF), as measured by DSC-MRIBaselineCox proportional hazards regression will be used to assess the association of CBF with change in tumor size.
Mean transit time (MTT), as measured by DSC-MRIBaselineCox proportional hazards regression will be used to assess the association of MTT with change in tumor size.
Cerebral blood volume (CBV), as measured by DSC-MRIBaselineCox proportional hazards regression will be used to assess the association of CBV with change in tumor size.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026