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Safety Study of Intracerebral Topotecan for Recurrent Brain Tumors

Primary Purpose

Brain Neoplasms, Primary Malignant

Status
Unknown status
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Convection-Enhanced Delivery
Topotecan
Sponsored by
Jeffrey N. Bruce
About
Eligibility
Locations
Arms
Outcomes
Full info

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

1 Year - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Arm Label

Topotecan

Arm Description

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.

Outcomes

Primary Outcome Measures

Time to tumor progression/recurrence
Time to death
Grade 3 Adverse Events

Secondary Outcome Measures

Quality of life at follow-up time points

Full Information

First Posted
March 27, 2006
Last Updated
January 13, 2015
Sponsor
Jeffrey N. Bruce
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1. Study Identification

Unique Protocol Identification Number
NCT00308165
Brief Title
Safety Study of Intracerebral Topotecan for Recurrent Brain Tumors
Official Title
A Phase I Study of Topotecan by Intracerebral Clysis for the Treatment of Recurrent Primary Malignant Brain Tumors
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Unknown status
Study Start Date
March 2004 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jeffrey N. Bruce

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will evaluate the safety and efficacy of a chemotherapeutic drug (topotecan) as it is given directly into brain tumors by a delivery technique called convection-enhanced delivery. This drug has been used for different types of cancer, but in this study it will be given by an experimental delivery technique designed to maximize the amount of drug delivered to the brain tumor and minimize the side effects in other parts of the body. This study will also evaluate advanced magnetic resonance (MR) imaging techniques. The study will assess quality of life parameters throughout the follow-up period.
Detailed Description
Clinical efficacy with chemotherapy has been discouraging for malignant brain tumors, mostly because of side effects and delivery limitations. Because they are locally invasive and rarely metastasize, malignant gliomas have features that make them uniquely amenable to new strategies of regional drug delivery. Intracerebral clysis (convection-enhanced delivery) is a novel drug delivery strategy that uses a microinfusion pump to establish a pressure gradient in the brain via implanted catheters. The pressure gradient produces convective forces that distribute a therapeutic agent throughout the tumor and surrounding brain tissue. Non-invasive magnetic resonance imaging (MRI) methods of monitoring drug distribution and treatment response have been developed to maximize the clinical applications and minimize complications associated with treatment risks. Study participants will be taken to the operating room to have 2 catheters surgically placed into their tumor and surrounding tumor bed. These catheters will then be connected to small infusion pumps which will slowly infuse topotecan continuously over 4-5 days. Patients will have daily MRI scans while in the hospital. Upon completion of the experimental treatment, patients will be discharged and will be followed up in the outpatient clinic.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Neoplasms, Primary Malignant
Keywords
Recurrent Primary Malignant Brain Tumors, Brain Tumors, Neoplasms, Brain, Brain Cancer, Brain cancer treatment, Topotecan

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Topotecan
Arm Type
Experimental
Arm Description
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.
Intervention Type
Procedure
Intervention Name(s)
Convection-Enhanced Delivery
Other Intervention Name(s)
Intracerebral Clysis
Intervention Description
microinfusion pumps to deliver chemotherapy directly into brain tumors
Intervention Type
Drug
Intervention Name(s)
Topotecan
Other Intervention Name(s)
Hycamtin
Intervention Description
chemotherapeutic drug for the treatment of brain tumors
Primary Outcome Measure Information:
Title
Time to tumor progression/recurrence
Time Frame
treatment to progression
Title
Time to death
Time Frame
Treatment to time of death
Title
Grade 3 Adverse Events
Time Frame
during treatment, post treatment
Secondary Outcome Measure Information:
Title
Quality of life at follow-up time points
Time Frame
pre-treatment, during treatment, post treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey Bruce, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Medical Center Neurological Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23240851
Citation
Anderson RC, Kennedy B, Yanes CL, Garvin J, Needle M, Canoll P, Feldstein NA, Bruce JN. Convection-enhanced delivery of topotecan into diffuse intrinsic brainstem tumors in children. J Neurosurg Pediatr. 2013 Mar;11(3):289-95. doi: 10.3171/2012.10.PEDS12142. Epub 2012 Dec 14.
Results Reference
derived

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Safety Study of Intracerebral Topotecan for Recurrent Brain Tumors

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