Gemcitabine in Treating Children With Refractory Solid Tumors
- Conditions
- Unspecified Childhood Solid Tumor, Protocol Specific
- Interventions
- Registration Number
- NCT00005577
- Lead Sponsor
- National Cancer Institute (NCI)
- Brief Summary
Phase I trial to study the effectiveness of gemcitabine in treating children who have refractory solid tumors. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.
- Detailed Description
OBJECTIVES:
I. Estimate the maximum tolerated dose of gemcitabine in children and adolescents with refractory solid tumors.
II. Assess the toxicity of gemcitabine in this patient population. III. Determine the pharmacokinetic profile of gemcitabine in male and female children and adolescents.
IV. Assess the antitumor activity of gemcitabine within a phase I study.
OUTLINE: This is a dose escalation study.
Patients receive gemcitabine IV over 30 minutes weekly for 2 weeks. Patients achieving objective response or stable disease after 3 weeks may receive additional courses of therapy every 3 weeks in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of gemcitabine until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose limiting toxicity. Patients are followed at week 4 and then every 6 months until death.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Arm I gemcitabine hydrochloride Patients receive gemcitabine IV over 30 minutes weekly for 2 weeks. Patients achieving objective response or stable disease after 3 weeks may receive additional courses of therapy every 3 weeks in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of gemcitabine until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose limiting toxicity.
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (23)
Children's Hospital of Orange County
πΊπΈOrange, California, United States
Princess Margaret Hospital for Children
π¦πΊPerth, Western Australia, Australia
Memorial Sloan-Kettering Cancer Center
πΊπΈNew York, New York, United States
Children's Hospital Los Angeles
πΊπΈLos Angeles, California, United States
Children's National Medical Center
πΊπΈWashington, District of Columbia, United States
University of Wisconsin Comprehensive Cancer Center
πΊπΈMadison, Wisconsin, United States
Jonsson Comprehensive Cancer Center, UCLA
πΊπΈLos Angeles, California, United States
Children's Hospital Medical Center - Cincinnati
πΊπΈCincinnati, Ohio, United States
UCSF Cancer Center and Cancer Research Institute
πΊπΈSan Francisco, California, United States
Cancer Center and Beckman Research Institute, City of Hope
πΊπΈLos Angeles, California, United States
Indiana University Cancer Center
πΊπΈIndianapolis, Indiana, United States
University of Michigan Comprehensive Cancer Center
πΊπΈAnn Arbor, Michigan, United States
University of Minnesota Cancer Center
πΊπΈMinneapolis, Minnesota, United States
Children's Mercy Hospital
πΊπΈKansas City, Missouri, United States
Mayo Clinic Cancer Center
πΊπΈRochester, Minnesota, United States
NYU School of Medicine's Kaplan Comprehensive Cancer Center
πΊπΈNew York, New York, United States
Herbert Irving Comprehensive Cancer Center
πΊπΈNew York, New York, United States
Children's Hospital of Philadelphia
πΊπΈPhiladelphia, Pennsylvania, United States
Vanderbilt-Ingram Cancer Center
πΊπΈNashville, Tennessee, United States
University of Texas - MD Anderson Cancer Center
πΊπΈHouston, Texas, United States
Children's Hospital of Pittsburgh
πΊπΈPittsburgh, Pennsylvania, United States
Huntsman Cancer Institute
πΊπΈSalt Lake City, Utah, United States
Children's Hospital and Regional Medical Center - Seattle
πΊπΈSeattle, Washington, United States