Depression, Neurotoxicity, Unspecified Childhood Solid Tumor, Protocol Specific
Conditions
Keywords
unspecified childhood solid tumor, protocol specific, depression, neurotoxicity
Brief summary
RATIONALE: Stimulant drugs such as dextroamphetamine-amphetamine and methylphenidate may help improve memory, attention, and thinking problems caused by central nervous system (CNS) treatment for cancer, and may help decrease depression. PURPOSE: This randomized phase II trial is studying dextroamphetamine-amphetamine to see how well it works compared to methylphenidate in treating depression and problems with memory, attention, and thinking in children who have undergone CNS treatment for cancer. This trial will also study how often depression is seen and if these medications might help.
Detailed description
OBJECTIVES: * Compare the response rates in pediatric cancer patients with treatment-related neurocognitive sequelae treated with dextroamphetamine-amphetamine (Adderall-XR®) vs methylphenidate (Concerta®). * Compare the durability of response at 12 weeks in patients who show a response at 3 weeks after treatment with these drugs. * Determine whether patients who have no response to one of these study drugs can respond to the other study drug. * Determine the prevalence of depression and possible response to neurostimulant therapy in this patient population. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive oral dextroamphetamine-amphetamine once daily for 3 weeks. Patients who achieve response (based on neurocognitive testing) continue treatment for a total of 12 weeks. Patients with no response after 3 weeks cross over to arm II after a 48-hour washout period. * Arm II: Patients receive oral methylphenidate once daily for 3 weeks. Responding patients continue treatment for a total of 12 weeks. Patients with no response after 3 weeks cross over to arm I after a 48-hour washout period. Depression and neurocognitive function are assessed at baseline, 3 weeks, and end of study. PROJECTED ACCRUAL: A total of 177 patients (approximately 88 per treatment arm) will be accrued for this study within 3 years.
Interventions
DRUGAdderall-XR®
Adderall-XR® 10 mg/day for 3-12 weeks depending on subject's response
DRUGConcerta®
Concerta® 18 mg/day for 3-12 weeks depending on subject's response
Sponsors
National Cancer Institute (NCI)
University of South Florida
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
6 Years to 17 Years
Healthy volunteers
No
Inclusion criteria
* Between the ages of 6-17 at the time of study participation. * Have a diagnosis of any malignancy that required CNS treatment such as surgery and/or irradiation and/or intrathecal chemotherapy. (Patients treated with systemic chemotherapy alone are not eligible to participate) * Off treatment and cancer free for a minimum of 6 months. * Have a proficiency in English.
Exclusion criteria
* Patients with an estimated intelligence quotient (IQ) of less than 65 (based on the Wide Range Achievement Test (WRAT-3) Reading subtest) are not eligible to continue on study. * At least one standard deviation below the level of performance predicted by their IQ on at least 2 of the 3 WISC-III subtests. * Diagnosed with Attention Deficit Disorder (ADD) or Attention Deficit Hyperactivity Disorder (ADHD) prior to their cancer diagnosis. * Currently taking antidepressants, antipsychotics, or other stimulants. * Are blind. * Have glaucoma. * Family history of motor and phonic tics or Tourette's syndrome. * Have seizures not controlled by antiepileptic drugs. (Note: Patients who are not experiencing seizure activity, having been on a stable dose of an antiepileptic drug for at least 12 weeks may participate) * Taking a monoamine oxidase (MAO) inhibitor. * Have a history of cardiovascular disease, uncontrolled hypertension or hyperthyroidism.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Response rate as measured by Wechsler Intelligence Scale for Children-III (WISC III) subtest: Coding, Symbol Search and Digit Span at baseline, and 3 weeks after the start of study treatment | 12 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Durability of response as measured by WISC III subtest: Coding, Symbol Search and Digit Span at 12 weeks after the start of study treatment | 12 weeks |
| Depression as measured by Children's Depression Inventory Short Version (CDI-S) at baseline, weeks 3 and 12 | 12 weeks |
Countries
United States
Outcome results
None listed