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Clinical Trials/NCT00047294
NCT00047294
Completed
Phase 2

Phase II Study Of Temozolomide, Thalidomide And Celecoxib In Patients With Newly Diagnosed Glioblastoma Multiforme In The Post-Radiation Setting

Dana-Farber Cancer Institute4 sites in 1 countryApril 2001

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Brain and Central Nervous System Tumors
Sponsor
Dana-Farber Cancer Institute
Locations
4
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Thalidomide and celecoxib may stop the growth of tumor cells by stopping blood flow to the tumor and may increase the effectiveness of temozolomide by making tumor cells more sensitive to the drug.

PURPOSE: Phase II trial to study the effectiveness of combining temozolomide, thalidomide, and celecoxib following radiation therapy in treating patients who have newly diagnosed glioblastoma multiforme.

Detailed Description

OBJECTIVES: * Determine the efficacy of adjuvant temozolomide, thalidomide, and celecoxib after radiotherapy, in terms of time to tumor progression and overall survival, in patients with newly diagnosed glioblastoma multiforme. * Determine the toxicity of this regimen in these patients. OUTLINE: This is a multicenter study. Patients receive oral temozolomide once daily on days 1-5 and oral thalidomide once daily and oral celecoxib twice daily on days 1-28. Treatment repeats every 28 days for up to 24 courses in the absence of disease progression or unacceptable toxicity. Patients are followed for survival. PROJECTED ACCRUAL: A total of 55 patients will be accrued for this study.

Registry
clinicaltrials.gov
Start Date
April 2001
End Date
September 2007
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Patrick Y. Wen, MD

Director, Center for Neuro-Oncology

Dana-Farber Cancer Institute

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (4)

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