Exploratory Study, Evaluating the Treatment Effect of Surgery Plus GLIADEL® Wafer in Patients With Metastatic Brain Cancer

Completed · Phase 2

Conditions studied: Metastatic Brain Cancer

In brief

The purpose of this study is to determine the effect of the surgical intervention and insertion of GLIADEL wafers on the neurocognitive functioning in patients with metastatic brain cancer.

Key facts

Study ID

NCT00525590

Run by

Eisai Inc.

People needed

69

Starts

2007-12-12

Expected to finish

2010-12-01

Last updated by the study team

2020-03-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Can provide signed/dated Informed Consent, and Health Insurance Portability and Accountability Act of 1996 (HIPAA) authorization.
• Are a male or female patient 18 years of age or older.
• Are willing to a use barrier method of contraception if fertile or of childbearing potential until 30 days after surgical resection. If the patient receives subsequent chemotherapy during study participation (as allowed by the protocol), appropriate contraception will be managed by the principal investigator.
• Have a primary diagnosis of solid-based tumor cancer (except small cell lung cancer (SCLS), lymphoma, germ cell cancer or anaplastic thyroid cancer) or unknown primary cancer and have 1-3 brain metastasis(es) for which surgical resection is planned for a single metastasis and any remaining metastases are planned for stereotactic radiosurgery (SRS);
• OR
• an intra-operative diagnosis of metastatic brain tumor in a patient with a single brain lesion.
• Have a life expectancy of ≥12 weeks.
• Have a Karnofsky Performance Status (KPS) score of 70 or higher.
• Have Recursive Partitioning Analysis (RPA) status of 1 or 2.
• Women of childbearing potential must have a negative serum or urine pregnancy test within 14 days of the surgical resection; and
• Patients must be able to understand English, either orally or in writing, and be able to consent and complete the required assessments and procedures.

You may not qualify if…

• Are unable or unwilling to understand study assessment or to cooperate with the study procedures as determined by the investigator.
• Have a history of allergic reaction or known hypersensitivity to BCNU (carmustine) or other components of the GLIADEL, such as polifeprosan polymer.
• Have a history of prior cranial irradiation.
• Have a prior diagnosis of Central Nervous System (CNS) tumor.
• Have received prior treatment for brain tumors.
• Have had prior exposure to GLIADEL or its components, such as polifeprosan polymer.
• Have any uncontrolled medical or psychiatric conditions which preclude them from participating in or completing the study procedures.
• Concurrent severe medical conditions include, but are not limited to, active infection, acute hepatitis, cardiac arrhythmia, unstable angina, congestive heart failure, uncontrolled diabetes mellitus, uncontrolled seizures, pulmonary insufficiency, pulmonary fibrosis, pulmonary embolus, etc.
• Have a diagnosis of tumor in the brain stem or posterior fossa.
• Have an RPA status of 3.
• Have a diagnosis of leptomeningeal disease at time of enrollment; or
• Are currently pregnant or lactating, or plan to become pregnant during the course of the study.

Where it is running

• University of Arizona / University Medical Center — Tucson, Arizona, United States
• University of California, Los Angeles — Los Angeles, California, United States
• University of South Florida — Tampa, Florida, United States
• H. Lee Moffitt Cancer Center & Research Institute — Tampa, Florida, United States
• The University of Chicago — Chicago, Illinois, United States
• NorthShore University HealthSystem Reseach Institute — Evanston, Illinois, United States
• University of Iowa Hospitals and Clinics — Iowa City, Iowa, United States
• Weill Medical College Department of Neurological Surgery — New York, New York, United States
• University of North Carolina — Chapel Hill, North Carolina, United States
• Carolina Neurosurgery & Spine Associates — Charlotte, North Carolina, United States
• Cleveland Clinic — Cleveland, Ohio, United States
• The Ohio State University Medical Center — Columbus, Ohio, United States
• Temple University — Philadelphia, Pennsylvania, United States
• Methodist University Hospital — Memphis, Tennessee, United States
• Vanderbilt University Medical Center — Nashville, Tennessee, United States
• UT Southwestern Medical Center at Dallas — Dallas, Texas, United States
• Trinity Mother Frances Health System — Tyler, Texas, United States

Full record on ClinicalTrials.gov

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