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Voxel Based Diffusion Tensor Imaging in Predicting Response in Patients With Brain Metastases Undergoing Whole Brain Radiation Therapy or Stereotactic Radiosurgery

Prediction of Response of Brain Metastases to Brain Irradiation Using Voxel Based Diffusion Tensor Imaging

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02277561
Enrollment
0
Registered
2014-10-29
Start date
2013-04-30
Completion date
2014-12-31
Last updated
2020-03-04

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 how well voxel based diffusion tensor imaging in predicting response in patients with brain metastases undergoing whole-brain radiation therapy or stereotactic radiosurgery. Voxel based diffusion tensor imaging (VB-DTI) may allow doctors to measure response to whole brain radiation therapy or stereotactic radiosurgery earlier than is possible with a standard magnetic resonance imaging. The earlier ability to measure response may allow for consideration of alternative therapies at an earlier stage.

Detailed description

PRIMARY OBJECTIVES: I. To determine if voxel based diffusion tensor imaging will provide an early predictive assessment of therapy response, as compared to radiographic volumetric response criteria. OUTLINE: Patients undergoing whole-brain radiation therapy (WBRT) for a total of 10 fractions also undergo VB-DTI magnetic resonance imaging (MRI) at baseline, 1 week after WBRT initiation, and 7-11 days after completion of WBRT. Patients undergoing stereotactic radiosurgery (SRS) without WBRT also undergo VB-DTI MRI at baseline and 7-11 days after completion of SRS. After completion of study, patients are followed up every 2 months for 6 months and then every 6 months until death.

Interventions

Undergo VB-DTI

Undergo WBRT

RADIATIONstereotactic radiosurgery

Undergo SRS

Undergo contrast-enhanced MRI

PROCEDUREdiffusion-weighted magnetic resonance imaging

Undergo DW MRI

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Albert Einstein College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients with multiple lesions from solid tumors on clinical MRI diagnosing the brain metastases may be treated with either WBRT or SRS if clinically indicated at the time of presentation but not both * Karnofsky performance status (KPS) \>= 70 * Patients presenting with brain metastases from a newly diagnosed cancer may have systemic disease (brain disease at the time of initial cancer diagnosis) * Patients with a history of cancer, but newly diagnosed brain metastases must have clinically stable systemic disease * If a biopsy is performed, the patient has to be at least 1 week post-biopsy * The patient must be able to commit to diffusion-weighted magnetic resonance (MR) imaging, diffusion tensor imaging (DTI), and chemical shift imaging (CSI) prior to treatment, after the first week of treatment, and 7-11 days after the completion of treatment at the Magnetic Resonance Research Center (MRRC) * Patients undergoing SRS without WBRT must be able to commit to diffusion-weighted MR imaging, DTI, and CSI prior to treatment, and 7-11 days after the completion of the SRS treatment at the MRRC * The patient must also be able to commit to post-treatment follow-up visits at Montefiore Medical Center involving serial MR imaging; the follow-up visits are to occur bimonthly for 6 months and then every 6 months until death

Exclusion criteria

* Any medical condition, which would make the imaging studies or WBRT unsafe or poorly tolerated * Patient is receiving concurrent chemotherapy * Known allergic reaction to contrast or shellfish * Patients with brain metastases to be treated with radiosurgery * Patients with brain metastasis resulting from hematologic malignancies and small cell lung cancer * Implanted metal devices or foreign bodies that serve as a contraindication to MR imaging * Creatinine \> 1.4 mg/dl and creatinine clearance \< 20 mg/dl * Uncontrolled, clinically significant cardiac arrhythmias * Severe claustrophobia * Pregnant female * Any prior radiation therapy to the brain * KPS \< 70 * Patients with leptomeningeal disease

Design outcomes

Primary

MeasureTime frameDescription
Percentage of voxel-based mean apparent diffusion coefficient (ADC) increase per lesionUp to 3 years
Volume fraction of voxels showing treatment-related VB-DTI changes for each lesionAt 4 monthsSpearman's rank analysis will be used to determine if a correlation exists between the volume fraction of voxels showing treatment-related VB-DTI changes and the volumetric radiographic response for each lesion. Statistical significance will be achieved with a p value \< 0.05.
Volumetric radiographic response for each lesionAt 4 monthsSpearman's rank analysis will be used to determine if a correlation exists between the volume fraction of voxels showing treatment-related VB-DTI changes and the volumetric radiographic response for each lesion. Statistical significance will be achieved with a p value \< 0.05. Statistical significance will be achieved with a p value \< 0.05.
Change in a lesion's overall mean ADCBaseline to 4 monthsSpearman's rank analysis will be used to determine if a correlation exists between the volume fraction of voxels showing treatment-related VB-DTI changes and the volumetric radiographic response for each lesion. Statistical significance will be achieved with a p value \< 0.05. Statistical significance will be achieved with a p value \< 0.05.

Countries

United States

Outcome results

None listed

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