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Spots Global Cancer Trial Database for Temozolomide and Radiation Therapy in Treating Patients With Gliomas

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Trial Identification

Brief Title: Temozolomide and Radiation Therapy in Treating Patients With Gliomas

Official Title: A Phase II Study of a Temozolomide-Based Chemoradiotherapy Regimen for High-Risk Low-Grade Gliomas

Study ID: NCT00114140

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving temozolomide together with radiation therapy may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving temozolomide together with radiation therapy works in treating patients with low-grade gliomas.

Detailed Description: OBJECTIVES: * Compare the 3-year survival of patients with high-risk low-grade gliomas treated with temozolomide and radiotherapy followed by temozolomide alone with that of patients enrolled on European Organization for Research and Treatment of Cancer (EORTC)clinical trials EORTC-22844 and EORTC-22845. * Determine the toxicity of this regimen in these patients. * Determine the association between progression-free survival and O6-methylguanine-DNA methyltransferase (MGMT) methylation status in patients treated with this regimen. * Determine the association between survival and MGMT methylation status in patients treated with this regimen. * Determine the quality of life (QOL) of patients treated with this regimen. * Determine the neurocognitive function of patients treated with this regimen. * Evaluate the feasibility of collecting patient-reported QOL and neurocognitive assessments over 3 years. OUTLINE: This is a non-randomized, multicenter study. Patients receive oral temozolomide once daily on days 1-42 and undergo radiotherapy once daily on days 1-5, 8-12, 15-19, 22-26, 29-33, and 36-40, one hour before RT weekdays, in the evening weekends. Beginning 28 days after completion of chemoradiotherapy, patients receive oral temozolomide once daily on days 1-5. Treatment with temozolomide repeats every 28 days for up to 12 courses in the absence of disease progression or unacceptable toxicity. Quality of life is assessed at baseline, 6 months, 12 months. After completion of study treatment, patients are followed at 4 months, every 6 months for 2 years, and then annually thereafter. PROJECTED ACCRUAL: A total of 135 patients will be accrued for this study within 44 months.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arizona Oncology Services Foundation, Phoenix, Arizona, United States

USC/Norris Comprehensive Cancer Center and Hospital, Los Angeles, California, United States

CCOP - Christiana Care Health Services, Newark, Delaware, United States

University of Florida Shands Cancer Center, Gainesville, Florida, United States

Integrated Community Oncology Network, Jacksonville Beach, Florida, United States

Baptist Cancer Institute - Jacksonville, Jacksonville, Florida, United States

Integrated Community Oncology Network at Southside Cancer Center, Jacksonville, Florida, United States

Mayo Clinic - Jacksonville, Jacksonville, Florida, United States

Baptist Medical Center South, Jacksonville, Florida, United States

Integrated Community Oncology Network - Orange Park, Orange Park, Florida, United States

Florida Cancer Center - Palatka, Palatka, Florida, United States

Flagler Cancer Center, Saint Augustine, Florida, United States

University of Chicago Cancer Research Center, Chicago, Illinois, United States

DeCesaris Cancer Institute at Anne Arundel Medical Center, Annapolis, Maryland, United States

Greenebaum Cancer Center at University of Maryland Medical Center, Baltimore, Maryland, United States

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

Josephine Ford Cancer Center at Henry Ford Hospital, Detroit, Michigan, United States

West Michigan Cancer Center, Kalamazoo, Michigan, United States

Sparrow Regional Cancer Center, Lansing, Michigan, United States

Mayo Clinic Cancer Center, Rochester, Minnesota, United States

CCOP - Kansas City, Kansas City, Missouri, United States

Methodist Estabrook Cancer Center, Omaha, Nebraska, United States

Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

Mission Hospitals - Memorial Campus, Asheville, North Carolina, United States

Summa Center for Cancer Care at Akron City Hospital, Akron, Ohio, United States

Aultman Cancer Center at Aultman Hospital, Canton, Ohio, United States

Cleveland Clinic Taussig Cancer Center, Cleveland, Ohio, United States

Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Medical Center, Columbus, Ohio, United States

Cancer Research UK Medical Oncology Unit at Churchill Hospital & Weatherall Institute of Molecular Medicine - Oxford, Salem, Ohio, United States

Cancer Treatment Center, Wooster, Ohio, United States

Rosenfeld Cancer Center at Abington Memorial Hospital, Abington, Pennsylvania, United States

Penn State Cancer Institute at Milton S. Hershey Medical Center, Hershey, Pennsylvania, United States

Kimmel Cancer Center at Thomas Jefferson University - Philadelphia, Philadelphia, Pennsylvania, United States

CCOP - Upstate Carolina, Spartanburg, South Carolina, United States

Rapid City Regional Hospital, Rapid City, South Dakota, United States

Jon and Karen Huntsman Cancer Center at Intermountain Medical Center, Murray, Utah, United States

Dixie Regional Medical Center - East Campus, Saint George, Utah, United States

University Cancer Center at University of Washington Medical Center, Seattle, Washington, United States

Green Bay Oncology, Limited at St. Vincent Hospital Regional Cancer Center, Green Bay, Wisconsin, United States

St. Vincent Hospital Regional Cancer Center, Green Bay, Wisconsin, United States

Gundersen Lutheran Center for Cancer and Blood, La Crosse, Wisconsin, United States

University of Wisconsin Paul P. Carbone Comprehensive Cancer Center, Madison, Wisconsin, United States

Bay Area Cancer Care Center at Bay Area Medical Center, Marinette, Wisconsin, United States

Medical College of Wisconsin Cancer Center, Milwaukee, Wisconsin, United States

Hopital Notre-Dame du CHUM, Montreal, Quebec, Canada

McGill Cancer Centre at McGill University, Montreal, Quebec, Canada

Contact Details

Name: Barbara J. Fisher, MD

Affiliation: London Health Sciences Centre

Role: PRINCIPAL_INVESTIGATOR

Name: David R. Macdonald, MD, FRCPC

Affiliation: London Health Sciences Centre

Role: STUDY_CHAIR

Name: Glenn J. Lesser, MD

Affiliation: Wake Forest University Health Sciences

Role: STUDY_CHAIR

Name: Stephen W. Coons, MD

Affiliation: St. Joseph's Hospital and Medical Center, Phoenix

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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