A Study Comparing GLIADEL to Stereotactic Radiosurgery in Metastatic Brain Disease

Description

This study is being done to see if adding GLIADEL to the site where the tumor was removed works as well as just having the tumor removed with radiation treatment done within six weeks after the surgery to keep the cancer from coming back.

Conditions

Brain Tumor - Metastatic

Study Overview

Study Details

Study overview

This study is being done to see if adding GLIADEL to the site where the tumor was removed works as well as just having the tumor removed with radiation treatment done within six weeks after the surgery to keep the cancer from coming back.

A Randomized Trial Evaluating GLIADEL Compared to Stereotactic Radiosurgery in Subjects With Metastatic Brain Disease

A Study Comparing GLIADEL to Stereotactic Radiosurgery in Metastatic Brain Disease

Condition
Brain Tumor - Metastatic
Intervention / Treatment

-

Contacts and Locations

Detroit

Henry Ford, Detroit, Michigan, United States, 48202

Omaha

University of Nebraska Medical Center, Omaha, Nebraska, United States, 68198

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Age 18 years or older (Nebraska is 19 years or older)
  • 2. Karnofsky Performance Score ≥ 70
  • 3. RPA class I or II
  • 4. Known or suspected primary solid cancer with metastatic brain tumor(s) - up to four in number and up to 4 cm in size with surgical resection planned for one or two tumors.
  • 5. Adequate platelet count (≥ 100,000/mm3), transfusion permitted
  • 6. Laboratory values adequate for patient to undergo surgery, including: (transfusion permitted to reach goals)
  • 7. Women of childbearing potential must have a negative pregnancy test within 7 days of initiating study
  • 8. INR ≤ 1.3
  • 9. Estimated survival time of ≥ 3 months as determined by the patient's primary oncologist.
  • 10. The subject is willing and able to consent to and abide by the protocol.
  • 1. Prior treatment to the area of planned resection (surgery, radiation).
  • 2. Prior whole brain radiation therapy.
  • 3. Diagnosis of lymphoma, germ cell cancer, small cell lung cancer, anaplastic thyroid cancer.
  • 4. Leptomeningeal disease
  • 5. Neurodegenerative disorder (e.g. dementia).
  • 6. Tumor size \> 4 cm.
  • 7. RPA class III
  • 8. Inability or unwillingness to co-operate with the requirements of the protocol
  • 9. Any other clinically significant medical disease or condition laboratory abnormality or psychiatric illness that, in the Investigator's opinion, may interfere with protocol adherence or confound efficacy or safety assessment or a subject's ability to give informed consent.
  • 10. Participation in other therapeutic clinical trials
  • 11. Severe pulmonary, cardiac or other systemic disease, specifically:
  • 1. New York Heart Association \> Grade 2 congestive heart failure within 6 months prior to study entry, unless asymptomatic and well controlled with medication
  • 2. Uncontrolled or significant cardiovascular disease, clinically significant ventricular arrhythmia, clinically significant pulmonary disease
  • 12. Subjects who have any other disease, either metabolic or psychological, which as per the Investigator assessment may affect the subject's compliance or place the subject at higher risk of potential treatment complications.
  • 13. The subject has a bleeding diathesis, or must take anticoagulants, or antiplatelet agents including NSAIDs (non-steroidal anti-inflammatory drugs), at the time of scheduled resection that cannot be stopped for surgery.
  • 14. Inability to obtain MRI studies.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Nebraska,

Michele Aizenberg, MD, PRINCIPAL_INVESTIGATOR, University of Nebraska

Study Record Dates

2026-12