SLEEP, FATIGUE, AND DEXAMETHOSONE IN CHILDHOOD CANCER
SLEEP, FATIGUE, AND DEXAMETHOSONE IN CHILDHOOD CANCER
批准号:
6393115
负责人:
Pamela S Hinds
金额:
$26.32万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-09-30 至 2004-06-30
关键词:
acute lymphocytic leukemia adolescence (12-20) age difference blood chemistry clinical research dexamethasone dosage drug administration rate /duration drug adverse effect drug screening /evaluation fatigue gender difference genetic polymorphism human subject human therapy evaluation middle childhood (6-11) neoplasm /cancer chemotherapy patient monitoring device pediatric neoplasm /cancer personal log /diary pharmacogenetics pharmacokinetics preschool child (1-5) questionnaires sleep disorders
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Mounting evidence indicates that adding dexamethasone to the
therapy for children and adolescents diagnosed with lymphoblastic leukernia
contributes to more positive long-term outcomes such as lower rates of
meningeal leukemia. The significant positive contributions of dexamethasone
have not occurred without adverse effects including avascular necrosis. mania
and psychosis, and aberrant sleep and fatigue. These adverse effects could be
related to inter-individual variability in the systemic exposure to
dexamethasone and if so, the adverse effects could serve as behavioral
indicators of patient sensitivity to the dosing schedule. To determine whether
dexamethasone dosing schedules need to be individualized to minimize adverse
effects while maintaining antileukernic effects, the relationship between
inter-individual variability and adverse effects must be established. The
overall purpose of this two-site study is to determine the relationship between
systemic exposure to dexamethasone and patients' sleep and fatigue by comparing
multiple indicators of patient sleep and fatigue in two consecutive 5-day
periods during Continuation therapy off and on dexatnethasone. Approximately
134 children and adolescents with low or standard fisk ALL will wear a wnist
actigraph for the two consecutive 5-day study periods and will complete a
self-report fatigue questionnaire during a telephone interview on Days 2 and 5
of both study periods. Their parents will complete a sleep diary and a fatigue
questionnaire on Days 2 and 5 of both study periods regarding their child's
sleep and fatigue patterns. In addition, on Day I of the on dexamethasone 5-day
study period, patients will-have sequential blood samples collected pre- and
post- the morning dose of dexamethasone. These samples will be analyzed for
dexamethasone pharmacokinetics and genetic polymorphism. Using these data, we
will test the hypothesis that dexamethasone contributes to aberrant sleep and
increased fatigue in children and adolescents with ALL, and that the altered
sleep and fatigue are related to the pharmacokinetics of the drug. Our study
findings will explicate the relationship between sleep efficiency and fatigue,
and between sleep, fatigue, and systemic exposure to dexamethasone.
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