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.
Brief Title
Voxel Based Diffusion Tensor Imaging in Predicting Response in Patients With Brain Metastases Undergoing Whole Brain Radiation Therapy or Stereotactic Radiosurgery
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.
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.
Categories
Completion Date
Completion Date Type
Actual
Conditions
Tumors Metastatic to Brain
Unspecified Adult Solid Tumor, Protocol Specific
Eligibility Criteria
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
* 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
Inclusion Criteria
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
* 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
Gender
All
Gender Based
false
Healthy Volunteers
No
Last Update Post Date
Last Update Post Date Type
Actual
Last Update Submit Date
Minimum Age
19 Years
NCT Id
NCT02277561
Org Class
Other
Org Full Name
Albert Einstein College of Medicine
Org Study Id
13-01-047
Overall Status
Withdrawn
Phases
Not Applicable
Primary Completion Date
Primary Completion Date Type
Actual
Official Title
Prediction of Response of Brain Metastases to Brain Irradiation Using Voxel Based Diffusion Tensor Imaging
Primary Outcomes
Outcome Measure
Percentage of voxel-based mean apparent diffusion coefficient (ADC) increase per lesion
Outcome Time Frame
Up to 3 years
Outcome Description
Spearman'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.
Outcome Measure
Volume fraction of voxels showing treatment-related VB-DTI changes for each lesion
Outcome Time Frame
At 4 months
Outcome Description
Spearman'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.
Outcome Measure
Volumetric radiographic response for each lesion
Outcome Time Frame
At 4 months
Outcome Description
Spearman'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.
Outcome Measure
Change in a lesion's overall mean ADC
Outcome Time Frame
Baseline to 4 months
Secondary Ids
Secondary Id
NCI-2014-01015
Secondary Id
13-01-047
Secondary Id
P30CA013330
Start Date
Status Verified Date
First Post Date
First Post Date Type
Estimated
First Submit Date
First Submit QC Date
Std Ages
Adult
Older Adult
Maximum Age Number (converted to Years and rounded down)
999
Minimum Age Number (converted to Years and rounded down)
19
Investigators
Investigator Type
Principal Investigator
Investigator Name
Wolfgang Tome
Investigator Email
wtome@montefiore.org
Investigator Phone
WTOME