The primary purpose of the study is to evaluate if motexafin gadolinium with whole brain radiation therapy followed by a stereotactic radiosurgery boost is a safe and effective treatment.
Patients will receive three weeks of whole brain radiation therapy concurrent with daily motexafin gadolinium during weeks 2 and 3, followed by a stereotactic radiosurgery boost concurrent with motexafin gadolinium. Patients will be followed for radiologic response, neurologic progression, and neurocognitive progression.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
45
Unnamed facility
Phoenix, Arizona, United States
Unnamed facility
Aurora, Colorado, United States
Unnamed facility
Cleveland, Ohio, United States
Unnamed facility
Columbus, Ohio, United States
Rate of irreversible Grade 3 or any Grade 4 or 5 neurologic radiation toxicities occuring within 3 months following SRS boost
Change in lesion size and number between screening MRI and SRS treatment -planning MRI
Time to neuroligic progression or death with evidence of neurologic progression
Time to neurocognitive progression
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Unnamed facility
Philadelphia, Pennsylvania, United States
Unnamed facility
Dallas, Texas, United States
Unnamed facility
Houston, Texas, United States
Unnamed facility
Madison, Wisconsin, United States
Unnamed facility
Milwaukee, Wisconsin, United States
Unnamed facility
Montreal, Quebec, Canada
...and 2 more locations