A Pilot Trial of Intraparenchymally-Administered Topotecan Using Convection-Enhanced Delivery (CED) in Patients With Suspected Recurrent/Progressive WHO Grade III or IV (High Grade) Glioma Requiring Stereotactic Biopsy
Overview
- Phase
- Early Phase 1
- Intervention
- Topotecan
- Conditions
- Malignant Glioma
- Sponsor
- Michael Vogelbaum, MD, PhD
- Enrollment
- 3
- Locations
- 1
- Primary Endpoint
- Spatial distribution of topotecan
- Status
- Completed
- Last Updated
- 9 years ago
Overview
Brief Summary
Topotecan is a FDA-approved drug when given by intravenous injection, but it is not effective against brain tumors when given intravenously. The Cleveland Multiport Catheter is a new, investigational device that will be used to deliver topotecan directly into participants' brain tumors. One purpose of this study is to determine whether the Cleveland Multiport Catheter can be used effectively and safely to deliver topotecan directly into brain tumors. This study will also evaluate different doses of topotecan that can be delivered to a participant's brain tumor with use of the Cleveland Multiport Catheter, and it will also examine how their tumor responds to treatment with topotecan.
Detailed Description
This study will look at the way topotecan is injected into participant's tumor. A small amount of contrast dye (called gadolinium DTPA) will be added to topotecan before it is injected. Pictures will be taken of the tumor with an MRI machine. This will allow the investigators to see where in the tumor the topotecan has been injected. Issues related to patient selection, coordination with other therapeutic and palliative clinical options, and patient quality of life impact will be studied. Except for the infusion of topotecan and gadolinium DTPA into the tumor, and MRI imaging of the infusion process, all procedures and treatments participants will experience during the care of their brain tumor are non-investigational; the types of medical treatments, procedures, and tests they experience will be Standard of Care for patients with brain tumors. Primary Objectives: * To investigate by MR imaging the spatial and temporal distribution of topotecan in tumor and tumor-infiltrated brain administered by convection-enhanced delivery (CED) in patients with recurrent/progressive WHO grade III or IV (high grade) glioma (HGG) who have failed standard therapy comprising surgical biopsy and/or resection and adjuvant chemotherapy and radiotherapy * To investigate by MR imaging the influence of the rate and topotecan concentration, on the spatial and temporal distribution of topotecan administered by CED in patients with recurrent/progressive HGG * To evaluate the spatial and temporal distribution of topotecan, by MR imaging, when delivered into enhancing tumor tissue versus non-enhancing tumor tissue (as defined on pre-operative conventional MRI imaging with and without intravenous gadolinium) Secondary Objectives: * To investigate the extent to which backflow may be observed on MRI during CED-mediated delivery of topotecan * To assess the safety, tolerability and toxicity profile of topotecan administered by CED using different doses and infusion rates * To observe evidence of activity of single-agent topotecan administered by CED to patients with recurrent/progressive HGG who have failed standard therapy comprising surgical biopsy and/or resection and adjuvant chemotherapy and radiotherapy
Investigators
Michael Vogelbaum, MD, PhD
Principal Investigator
Case Comprehensive Cancer Center
Eligibility Criteria
Inclusion Criteria
- •Histologically confirmed diagnosis of supratentorial WHO Grade III or IV (High Grade Glioma) that has undergone surgical biopsy or resection followed by adjuvant chemoradiotherapy, that has evidence of recurrence or progression based on imaging studies and a stereotactic biopsy is indicated for confirmation of recurrence/progression
- •Karnofsky Performance Status 70-100
- •MRI demonstration of a stereotactically accessible enhancing mass of less than 40cm3 that does not require resection to relieve clinically significant mass effect
- •Patient understands the procedures and agrees to comply with the study requirements by providing written informed consent
- •Laboratory values within the following ranges:
- •Absolute neutrophil count (ANC)≥1,500/microliter
- •Platelet count≥100,000/microliter
- •Hemoglobin≥10g/dL
- •Normal PT/PTT
- •Estimated glomerular filtration rate (eGFR) of at least 50mL/min
Exclusion Criteria
- •Patient is mentally or legally incapacitated at the time of the study
- •Known HIV(+) or has been diagnosed with AIDS
- •Participation in another investigational drug study in the prior 4 weeks
- •Positive pregnancy test in a female
- •Patient, in the opinion of the investigator, is likely to be poorly compliant
- •Diffuse subependymal or CSF disease
- •Tumors involving the cerebellum
- •Tumor enhancement involving both hemispheres
- •Active infection requiring treatment
- •Unexplained febrile illness
Arms & Interventions
Direct infusion of topotecan
The experimental Cleveland Multiport Catheter will be used to inject a chemotherapy, topotecan, and a contrast agent, gadolinium DTPA, into the high grade brain tumors of study participants
Intervention: Topotecan
Direct infusion of topotecan
The experimental Cleveland Multiport Catheter will be used to inject a chemotherapy, topotecan, and a contrast agent, gadolinium DTPA, into the high grade brain tumors of study participants
Intervention: Gadolinium DTPA
Direct infusion of topotecan
The experimental Cleveland Multiport Catheter will be used to inject a chemotherapy, topotecan, and a contrast agent, gadolinium DTPA, into the high grade brain tumors of study participants
Intervention: Cleveland Multiport Catheter
Outcomes
Primary Outcomes
Spatial distribution of topotecan
Time Frame: 24 weeks
Determination of the spatial distribution of intraparenchymally-administered topotecan over time using a gadolinium-based contrast agent, volumetric magnetic resonance imaging, and three-dimensional image reconstruction
Number of catheter- and/or drug-related complications
Time Frame: 24 weeks
The overall number of catheter- and/or drug-related complications occurring intra-operatively, post-operatively, or following catheter removal
Secondary Outcomes
- Objective response rate of subjects given topotecan(24 weeks)
- Median overall survival of HGG subjects given topotecan(24 weeks)
- Median progression-free survival of HGG subjects given topotecan(24 weeks)
- Proportion of progression free HGG subjects given topotecan(24 weeks)