Solid Tumors
Conditions
Keywords
Refractory Childhood Solid Tumors
Brief summary
The purpose of this protocol is to estimate the maximum tolerated dose of gefitinib in combination with fixed dose of irinotecan and vincristine in patients with refractory solid tumors.
Detailed description
Objectives of this study are: * To determine the dose-limiting toxicities (DLT) of the combination of irinotecan and ZD1839 when given on this schedule. * To characterize the pharmacokinetics and pharmacodynamics of gefitinib alone and in combination with irinotecan and vincristine. * To estimate the maximum tolerated dose (MTD) of gefitinib in combination with escalating intravenous irinotecan by using selective intestinal decontamination with oral cefixime or cefpodoxime to prevent diarrhea. * To estimate the MTD of vincristine (MTD) in combination with gefitinib and irinotecan. Details of Treatment Interventions First Cohort: Standard dose escalation, starting at ZD1839 150 mg/m2/day for 21 days in combination with irinotecan 15mg/m2/day on a daily x 5 for two consecutive week schedule. Dose-limiting diarrhea was seen in this cohort. ZD scheduled was reduced to 12 days. The first dose level (1a) consisted of ZD1839 112.5mg/m2/day for 12 days + irinotecan 15mg/m2/day daily x 5 x 2 and was found to be the MTD in this cohort. Second Cohort: Cefixime then added at 4 additional subjects were enrolled at dose level 1c, consisting of ZD1839 at 112mg/m2/day + irinotecan 20mg/m2/day + cefixime 8 mg/kg/day administered once daily, beginning on day -1, and continued to day 14. Third Cohort: Irinotecan/ZD1839/Vincristine/Cefixime- Cefixime 8 mg/kg/day administered once daily, beginning on day -1, and continued to day 14, with a maximum dose of 400 mg daily + gefitinib 112.5 mg/m2 orally, daily for 12 days and irinotecan at 15 mg/m2 daily x 5 x 2 +1 mg/m2 (maximum 2mg/dose) on days 1 and 8 with escalating dose of VCR as tolerated.
Interventions
DRUGIrinotecan, ZD1839, Vincristine, Cefixime, Cefpodoxime.
See Detailed Description section for details of treatment interventions.
Sponsors
AstraZeneca
National Institutes of Health (NIH)
St. Jude Children's Research Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
No minimum to 21 Years
Healthy volunteers
No
Inclusion criteria
* Younger than 22 years of age. * Histologic verification of solid tumor malignancy at original diagnosis. * Has disease considered refractory to conventional therapy or no conventional therapy exists. * Adequate performance status, bone marrow, liver and kidney function. * Patients must not have had any previous allergic reactions to penicillin or cephalosporins
Exclusion criteria
* Known severe hypersensitivity to ZD1839 or any of the excipients of this product * Concomitant use of phenytoin, carbamazepine, barbiturates, rifampicin, phenobarbital, or St John's Wort, and CYP3A4 inhibitors * Treatment with a non-approved or investigational drug within 30 days before Day 1 of trial treatment. * Incomplete healing from previous oncologic or other major surgery * Pregnant or breast-feeding * Patients who have an uncontrolled infection * Any evidence of clinically active interstitial lung disease (patients with chronic stable radiographic changes who are asymptomatic need not be excluded). * As judged by the investigator, any evidence of uncontrolled systemic disease (e.g., unstable or uncompensated respiratory, cardiac, hepatic, or renal disease). * Evidence of any other significant clinical disorder or laboratory finding that makes is undesirable for the subject to participate in the trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dose limiting toxicities | Within the first 30 days of completion of first cycle |
Countries
United States
Outcome results
None listed