Donepezil and Vitamin E to Prevent Side Effects Caused By Radiation Therapy to the Head in Patients Receiving Treatment for Small Cell Lung Cancer
Cognitive/Functional Effects, Delirium, Depression
About this trial
This is an interventional supportive care trial for Cognitive/Functional Effects focused on measuring depression, delirium, cognitive/functional effects, radiation toxicity, limited stage small cell lung cancer, extensive stage small cell lung cancer, recurrent small cell lung cancer
Eligibility Criteria
DISEASE CHARACTERISTICS: Diagnosis of small cell lung cancer (SCLC) Must meet one of the following conditions: Enrolled no more than 4 weeks before initiation of prophylactic cranial irradiation (PCI) OR Enrolled no more than 10 days after initiation of PCI Limited or extensive stage SCLC with complete response (CR) outside chest allowed Must have CR or minimal disease after completion of intended course of chemotherapy No disease progression since initiation of PCI No prior or concurrent CNS metastases PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: At least 12 weeks Hepatic: Bilirubin no greater than 1.5 mg/dL Renal: Creatinine no greater than 2 times upper limit of normal Cardiovascular: No sick sinus syndrome or other symptomatic supraventricular conduction disorders even if symptoms currently controlled by antiarrhythmics Pulmonary: No history of asthma or chronic obstructive pulmonary disease requiring chronic oxygen therapy Other: No medical or psychiatric condition that would increase risk No seizure disorder No ongoing alcohol abuse PRIOR CONCURRENT THERAPY: Chemotherapy: See Disease Characteristics No concurrent anticancer chemotherapy Other: No concurrent medications that would impair baseline cognitive function or are likely to be dose escalated over the next few months No other concurrent vitamin E
Sites / Locations
- CCOP - Scottsdale Oncology Program
- Mayo Clinic
- CCOP - Illinois Oncology Research Association
- CCOP - Carle Cancer Center
- CCOP - Cedar Rapids Oncology Project
- CCOP - Iowa Oncology Research Association
- Siouxland Hematology-Oncology
- CCOP - Wichita
- Mayo Clinic Cancer Center
- CCOP - Missouri Valley Cancer Consortium
- Medcenter One Health System
- CCOP - Merit Care Hospital
- Allegheny General Hospital
- Rapid City Regional Hospital
- CCOP - Sioux Community Cancer Consortium
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
donepezil + vitamin E
placebo
Patients receive oral donepezil daily and vitamin E twice daily. All patients begin treatment within 2 weeks after completion of prophylactic cranial irradiation. Treatment continues for a minimum of 1 month in the absence of disease progression, unacceptable toxicity, or a 3.0 point drop on the Mini Mental State Examination (MMSE) and/or a 5 point drop on the Blessed Dementia Scale. Cognition is assessed using the Blessed Dementia Scale and the MMSE at baseline and then every 3 months during study. Quality of life and depression are assessed at baseline and then every 3 months during study. Patients are followed every 6 months.
Patients receive oral placebo twice daily. All patients begin treatment within 2 weeks after completion of prophylactic cranial irradiation. Treatment continues for a minimum of 1 month in the absence of disease progression, unacceptable toxicity, or a 3.0 point drop on the Mini Mental State Examination (MMSE) and/or a 5 point drop on the Blessed Dementia Scale. Cognition is assessed using the Blessed Dementia Scale and the MMSE at baseline and then every 3 months during study. Quality of life and depression are assessed at baseline and then every 3 months during study. Patients are followed every 6 months.