Safety Study of Intracerebral Topotecan for Recurrent Brain Tumors
Brain Neoplasms, Primary Malignant
About this trial
This is an interventional treatment trial for Brain Neoplasms, Primary Malignant focused on measuring Recurrent Primary Malignant Brain Tumors, Brain Tumors, Neoplasms, Brain, Brain Cancer, Brain cancer treatment, Topotecan
Eligibility Criteria
Inclusion Criteria: Single primary malignant brain tumor Previous treatment with external beam radiation Tumor is stereotactically accessible Karnofsky Performance Score of at least 60 Exclusion Criteria: Diffuse subependymal or Cerebrospinal fluid (CSF) disease Tumor involves brainstem, cerebellum or both hemispheres Active infection Systemic disease associated with unacceptable anesthetic/operative risk Previous treatment with topotecan Unable to receive MRI scans
Sites / Locations
- Columbia University Medical Center Neurological Institute
Arms of the Study
Arm 1
Experimental
Topotecan
Once a plastic catheter is placed, within 24 hours of placement, the catheter will be connected to a small pump at the bedside, and the convection-enhanced delivery of the Topotecan will begin. The Topotecan will be infused for 4 to 5 days after which time the catheters will simply be pulled out. Patients will be monitored with blood tests and MRI scans during the treatment and at different time periods during the following months.