⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for High-Dose Chemotherapy Plus Autologous Stem Cell Transplantation Compared With Intermediate-Dose Chemotherapy Plus Autologous Stem Cell Transplantation With or Without Isotretinoin in Treating Young Patients With Recurrent High-Grade Gliomas

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: High-Dose Chemotherapy Plus Autologous Stem Cell Transplantation Compared With Intermediate-Dose Chemotherapy Plus Autologous Stem Cell Transplantation With or Without Isotretinoin in Treating Young Patients With Recurrent High-Grade Gliomas

Official Title: A Phase III Randomized Trial for the Treatment of Pediatric High Grade Gliomas at First Recurrence With a Single High Dose Chemotherapy and Autologous Stem Cell Transplant Versus Three Courses of Intermediate Dose Chemotherapy With Peripheral Blood Stem Cell (PBSC) Support

Study ID: NCT00078988

Study Description

Brief Summary: RATIONALE: Drugs used in chemotherapy, such as carboplatin, thiotepa, and etoposide, work in different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with autologous stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more tumor cells. Isotretinoin may be effective in preventing recurrence of glioma. It is not yet known which regimen of chemotherapy plus autologous stem cell transplantation with or without isotretinoin is more effective in treating recurrent high-grade glioma. PURPOSE: This randomized phase III trial is studying high-dose chemotherapy or intermediate-dose chemotherapy followed by autologous stem cell transplantation to see how well it works compared to high-dose chemotherapy or intermediate-dose chemotherapy followed by autologous stem cell transplantation and isotretinoin in treating young patients with recurrent high-grade glioma.

Detailed Description: OBJECTIVES: * Compare the event-free survival and overall survival of pediatric patients with recurrent high-grade gliomas treated with a single course of high-dose carboplatin, etoposide, and thiotepa and autologous stem cell transplantation vs multiple courses of intermediate-dose carboplatin and thiotepa and autologous stem cell transplantation with or without isotretinoin. * Compare the number of hospital days and time to engraftment in patients treated with these regimens. * Compare the toxic death rate in patients treated with these regimens. * Compare the tolerability of isotretinoin in patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to pathologic diagnosis (glioblastoma multiforme vs anaplastic astrocytoma vs other high-grade glioma). * Chemotherapy and autologous stem cell reinfusion (ASCR): Patients are randomized to 1 of 2 treatment arms. * Arm I (high-dose chemotherapy and ASCR): Patients receive high-dose chemotherapy comprising carboplatin IV over 4 hours on days -8 to -6; thiotepa IV over 3 hours and etoposide IV over 3 hours on days -5 to -3; and filgrastim (G-CSF) IV or subcutaneously (SC) once daily beginning on day 1 and continuing until blood counts recover. Autologous peripheral blood stem cells (PBSC) or bone marrow are reinfused on day 0. * Arm II (intermediate-dose chemotherapy and ASCR): Patients receive intermediate-dose chemotherapy comprising carboplatin IV over 4 hours and thiotepa IV over 3 hours on days 1-2 and G-CSF IV or SC once daily beginning on day 4 and continuing until blood counts recover. Autologous PBSC or bone marrow are reinfused on day 3. Treatment repeats every 28 days for a total of 3 courses. * Maintenance therapy: After recovery from chemotherapy (approximately day 30 post-transplantation), all patients are further randomized to 1 of 2 maintenance arms. * Arm I: Patients receive oral isotretinoin twice daily on days 1-14. Treatment repeats every 28 days for a total of 6 courses. * Arm II: Patients do not receive maintenance therapy. In all arms, treatment continues in the absence of disease progression. Patients are followed every 3 months for 1 year, every 6 months for 3 years, and then annually thereafter. PROJECTED ACCRUAL: A total of 80-150 patients (40-75 per treatment arm) will be accrued for this study within 5 years.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arkansas Cancer Research Center at University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States

Children's Hospital and Research Center - Oakland, Oakland, California, United States

University of California Davis Cancer Center, Sacramento, California, United States

Children's Hospital and Health Center - San Diego, San Diego, California, United States

Children's Hospital Cancer Center, Denver, Colorado, United States

Children's National Medical Center, Washington, District of Columbia, United States

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

Nemours Children's Clinic, Jacksonville, Florida, United States

University of Miami Sylvester Comprehensive Cancer Center, Miami, Florida, United States

Miami Children's Hospital, Miami, Florida, United States

All Children's Hospital, St. Petersburg, Florida, United States

St. Joseph's Cancer Institute at St. Joseph's Hospital, Tampa, Florida, United States

Kaplan Cancer Center at St. Mary's Medical Center, West Palm Beach, Florida, United States

Emory University Hospital - Atlanta, Atlanta, Georgia, United States

Cancer Research Center of Hawaii, Honolulu, Hawaii, United States

Indiana University Cancer Center, Indianapolis, Indiana, United States

St. Vincent Indianapolis Hospital, Indianapolis, Indiana, United States

Kosair Children's Hospital, Louisville, Kentucky, United States

CancerCare of Maine at Eastern Maine Medial Center, Bangor, Maine, United States

Floating Hospital for Children at Tufts - New England Medical Center, Boston, Massachusetts, United States

Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, United States

Spectrum Health Cancer Care - Butterworth Campus, Grand Rapids, Michigan, United States

Van Elslander Cancer Center at St. John Hospital and Medical Center, Grosse Pointe Woods, Michigan, United States

Children's Hospital of Minnesota - Minneapolis, Minneapolis, Minnesota, United States

Fairview University Medical Center - University Campus, Minneapolis, Minnesota, United States

University of Mississippi Medical Center, Jackson, Mississippi, United States

Children's Mercy Hospital, Kansas City, Missouri, United States

Siteman Cancer Center at Barnes-Jewish Hospital, St. Louis, Missouri, United States

Cancer Institute of New Jersey at UMDNJ - Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States

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

NYU Cancer Institute at New York University Medical Center, New York, New York, United States

Herbert Irving Comprehensive Cancer Center at Columbia University, New York, New York, United States

James P. Wilmot Cancer Center at University of Rochester Medical Center, Rochester, New York, United States

SUNY Upstate Medical University Hospital, Syracuse, New York, United States

New York Medical College, Valhalla, New York, United States

Children's Hospital Medical Center of Akron, Akron, Ohio, United States

Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States

Rainbow Babies and Children's Hospital, Cleveland, Ohio, United States

Columbus Children's Hospital, Columbus, Ohio, United States

Children's Medical Center - Dayton, Dayton, Ohio, United States

Oklahoma University Medical Center, Oklahoma City, Oklahoma, United States

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

Hollings Cancer Center at Medical University of South Carolina, Charleston, South Carolina, United States

Sioux Valley Hospital and University of South Dakota Medical Center, Sioux Falls, South Dakota, United States

Cook Children's Medical Center - Fort Worth, Fort Worth, Texas, United States

Covenant Children's Hospital, Lubbock, Texas, United States

Primary Children's Medical Center, Salt Lake City, Utah, United States

INOVA Fairfax Hospital, Fairfax, Virginia, United States

Children's Hospital of the King's Daughters, Norfolk, Virginia, United States

Massey Cancer Center at Virginia Commonwealth University, Richmond, Virginia, United States

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

Marshfield Clinic - Marshfield Center, Marshfield, Wisconsin, United States

Princess Margaret Hospital for Children, Perth, Western Australia, Australia

Children's & Women's Hospital of British Columbia, Vancouver, British Columbia, Canada

McMaster Children's Hospital at Hamilton Health Sciences, Hamilton, Ontario, Canada

Hospital for Sick Children, Toronto, Ontario, Canada

Montreal Children's Hospital at McGill University Health Center, Montreal, Quebec, Canada

Hopital Sainte Justine, Montreal, Quebec, Canada

Centre Hospitalier Universitaire de Quebec, Ste-Foy, Quebec, Canada

Contact Details

Name: Ziad Khatib, MD

Affiliation: Nicklaus Children's Hospital f/k/a Miami Children's Hospital

Role: STUDY_CHAIR

Name: Sharon L. Gardner, MD

Affiliation: NYU Langone Health

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: