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| Sponsored by: |
The Cleveland Clinic |
|---|---|
| Information provided by: | National Cancer Institute (NCI) |
| ClinicalTrials.gov Identifier: | NCT00096252 |
Purpose
RATIONALE: Internal radiation therapy uses radioactive material placed directly into or near a tumor to kill tumor cells. Stereotactic radiosurgery may be able to deliver x-rays directly to the tumor and cause less damage to normal tissue. Giving internal radiation therapy after surgery with or without radiosurgery may kill any remaining tumor cells.
PURPOSE: This phase II trial is studying how well internal radiation therapy with or without stereotactic radiosurgery works in treating patients who have undergone surgery for newly diagnosed brain metastases.
| Condition | Intervention | Phase |
|---|---|---|
|
Brain and Central Nervous System Tumors |
Procedure: conventional surgery Radiation: brachytherapy Radiation: stereotactic radiosurgery |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Open Label |
| Official Title: | A Phase II Study Utilizing Focal Radiation in Patients With 1-3 Brain Metastases |
| Estimated Enrollment: | 50 |
| Study Start Date: | December 2003 |
| Estimated Primary Completion Date: | October 2008 (Final data collection date for primary outcome measure) |
OBJECTIVES:
Primary
Secondary
OUTLINE: This is a multicenter study.
Patients undergo surgical resection of the metastatic brain lesion(s) followed by implantation of the GliaSite^® Radiation Therapy System (RTS).
Beginning within the 21 days after surgical resection, patients undergo brachytherapy using the GliaSite^® RTS over 3-7 days. Patients with tumor(s) remaining after surgery also undergo stereotactic radiosurgery 14-42 days after surgical resection and after completion of brachytherapy. Treatment continues in the absence of disease progression or unacceptable toxicity.
Quality of life is assessed at baseline, at 1 and 3 months, and then every 3 months for 2 years.
Patients are followed at 1 and 3 months and then every 3 months for 2 years.
PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
Histologically confirmed metastatic carcinoma
Newly diagnosed supratentorial metastatic brain lesions
PATIENT CHARACTERISTICS:
Age
Performance status
Life expectancy
Hematopoietic
Hepatic
Renal
Cardiovascular
Other
PRIOR CONCURRENT THERAPY:
Biologic therapy
Chemotherapy
Endocrine therapy
Radiotherapy
Surgery
Other
Contacts and Locations| United States, Ohio | |
| Cleveland Clinic Taussig Cancer Center | |
| Cleveland, Ohio, United States, 44195 | |
| Study Chair: | Michael A. Vogelbaum, MD, PhD | The Cleveland Clinic |
More Information
| Responsible Party: | Cleveland Clinic Taussig Cancer Center ( Michael A. Vogelbaum ) |
| Study ID Numbers: | CDR0000378193, CCF-IRB-6675, CCF-CTSRC-1007, PROXIMA-CCF-IRB-6675 |
| Study First Received: | November 9, 2004 |
| Last Updated: | February 6, 2009 |
| ClinicalTrials.gov Identifier: | NCT00096252 History of Changes |
| Health Authority: | United States: Federal Government |
|
adult tumors metastatic to brain |
|
Neoplasm Metastasis Central Nervous System Neoplasms Nervous System Neoplasms |
|
Neoplasms Neoplastic Processes Neoplasms by Site Pathologic Processes |
Nervous System Diseases Neoplasm Metastasis Central Nervous System Neoplasms Nervous System Neoplasms |