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Spots Global Cancer Trial Database for Temozolomide Plus Thalidomide in Treating Patients With Recurrent or Progressive Brain Tumor

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Temozolomide Plus Thalidomide in Treating Patients With Recurrent or Progressive Brain Tumor

Official Title: Phase II Evaluation of Temozolomide (SCH52365) and Thalidomide for the Treatment of Recurrent and Progressive Glioblastoma Multiforme

Study ID: NCT00006358

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Thalidomide may stop the growth of cancer by stopping blood flow to the tumor. PURPOSE: Phase II trial to study the effectiveness of combining temozolomide and thalidomide in treating patients who have recurrent or progressive brain tumor.

Detailed Description: OBJECTIVES: I. Determine the efficacy of temozolomide and thalidomide in patients with recurrent or progressive supratentorial glioblastoma multiforme or gliosarcoma. II. 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 daily on days 1-28. Treatment repeats every 28 days for a maximum of 24 courses in the absence of disease progression or unacceptable toxicity. Patients are followed at 1 month and then for survival. PROJECTED ACCRUAL: A total of 40 patients will be accrued for this study within 4-5 months.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, California, United States

UCSF Cancer Center and Cancer Research Institute, San Francisco, California, United States

Neuro-Oncology Branch, Bethesda, Maryland, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, United States

Memorial Sloan-Kettering Cancer Center, New York, New York, United States

University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania, United States

Simmons Cancer Center - Dallas, Dallas, Texas, United States

University of Texas - MD Anderson Cancer Center, Houston, Texas, United States

University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States

University of Wisconsin Comprehensive Cancer Center, Madison, Wisconsin, United States

Contact Details

Name: Morris D. Groves, MD, JD

Affiliation: M.D. Anderson Cancer Center

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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