Candidate mechanisms for chemotherapy-induced neurocognitive deficits in pediatric solid non-CNS tumor patients

儿童实体非中枢神经系统肿瘤患者化疗引起的神经认知缺陷的候选机制

• 批准号: 10285050
• 负责人: Travis E. Baker
• 金额: $ 18.35万
• 依托单位: RUTGERS THE STATE UNIV OF NJ NEWARK
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-07-05 至 2023-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10285050
• 关键词: 17 year old; Address; Adolescence; Adult; Adverse effects; Affect; Aftercare; Age; Area; Arousal; Attention; Awareness; Behavior; Behavioral; Biological Markers; Brain; Cancer Survivor; Carcinoma; Caring; Chemotherapy-Oncologic Procedure; Child; Childhood; Cognition; Cognitive; Cognitive deficits; Corpus striatum structure; Decision Making; Development; Dopamine; Early treatment; Electrophysiology (science); Exhibits; Family; Goals; Impaired cognition; Impairment; Learning; Lymphoblastic Leukemia; Lymphoma; Maintenance; Measurable; Measures; Medical; Modeling; Monitor; Negative Valence; Neuraxis; Neuroblastoma; Neurocognitive; Neurocognitive Deficit; Neurophysiology - biologic function; Patients; Pattern; Pediatric Oncology; Performance; Phenotype; Population; Positive Valence; Prefrontal Cortex; Process; Public Health; Research; Research Domain Criteria; Research Project Grants; Resources; Rewards; Short-Term Memory; Signal Transduction; Social Processes; Solid; Solid Neoplasm; Speed; Structure; Study models; Survival Rate; Survivors; Symptoms; Syndrome; System; Task Performances; Testing; Therapeutic Intervention; Time; Toxicity due to chemotherapy; Update; aged; base; cancer diagnosis; chemobrain; chemotherapeutic agent; chemotherapy; cognitive ability; cognitive control; cognitive function; cognitive system; cost; executive function; flexibility; follow-up; indexing; information processing; insight; memory process; neurotoxic; neurotoxicity; osteosarcoma; processing speed; recruit; relating to nervous system; response; reward processing; sex; therapy development; treatment strategy; virtual

1. Abstract Intensive curative chemotherapy is associated with subacute neurotoxicity, which can adversely affect brain functioning. These adverse treatment sequelae add to the significant lifelong impact on survivors and families, and may entail a measurable cost to societal, medical, and educational systems. To date, converging evidence shows that 40–70% of childhood survivors who have gone through central nervous system (CNS) chemotherapy exhibit deficits in attention, working memory, and information processing speed, deficits believed to be caused by the neurotoxicity of the treatment. While non-CNS solid tumors (NST) collectively account for over one third of cancer diagnoses among children, little is known about the neurotoxic effects of chemotherapy in NST survivors. The overarching goal of this project is to examine the impact of chemotherapy-related neurotoxicity on well-established neural, cognitive, and computational indices of reward processing, cognitive control and working memory in pediatric NST survivors. To achieve our goal, we aim to recruit 30 survivors of childhood NTS (e.g., osteosarcomas, lymphomas, carcinomas, and neuroblastomas) aged 6–17 years old and 30 age-matched typically developing children. The specific aims of this project will be to examine group differences between electrophysiological, behavioral, and computational biomarkers associated with reward responsiveness (Aim 1a), reward valuation (Aim 1b), cognitive control (Aim 2a) and working memory (Aim 2b). Our overarching hypothesis is that chemotherapy for NST alters neural activity and brain structures involved in specific cognitive functions (reward processing, cognitive control, working memory), and we predict that our selected neurocognitive indices of these functions will reveal unique patterns of abnormal neural and computational processes compared to healthy, age- and sex-matched controls. We believe that the diversity in these areas of research, such as engaging multiple neural systems, enables us to address basic, translational, and applied questions, including those at the intersection of the brain, computation, and behavior. Our long-term goal will be to find out whether this cross-cutting research model will aid in the development of a more targeted and efficient chemotherapy treatments for pediatric NST, as well as aftercare for cognitive deficits. By identifying such neurocognitive phenotypes, this research will help develop future research and grant strategies aimed at reducing the adverse effects of chemotherapy as well as tailor therapeutic interventions for the specific cognitive profile of this population.

1.摘要 强化根治性化疗与亚急性神经毒性有关，这会对大脑产生不利影响。 功能正常。这些不良治疗的后遗症增加了对幸存者和家属的重大终身影响， 并可能给社会、医疗和教育系统带来可衡量的成本。到目前为止，汇聚的证据 显示40%-70%的接受过中枢神经系统(CNS)化疗的儿童幸存者 表现出注意力、工作记忆和信息处理速度的缺陷，这些缺陷被认为是导致的 治疗的神经毒性。而非中枢神经系统实体瘤(NST)合计占三分之一以上 在儿童癌症诊断中，对NST化疗的神经毒性作用知之甚少 幸存者。这个项目的首要目标是检查化疗相关的神经毒性的影响。 关于奖赏加工、认知控制和计算的神经、认知和计算指标 儿童NST幸存者的工作记忆。为了实现我们的目标，我们的目标是招募30名儿童NTS幸存者 (例如，骨肉瘤、淋巴瘤、癌症和神经母细胞瘤)，年龄6-17岁，年龄30岁 通常是发育中的儿童。本项目的具体目标将是考察不同群体之间的差异 与奖励反应(AIM)相关的电生理、行为和计算生物标记物 奖励评估(目标1b)、认知控制(目标2a)和工作记忆(目标2b)。我们最重要的是 假说是NST的化疗改变了涉及特定认知的神经活动和脑结构 功能(奖赏处理、认知控制、工作记忆)，我们预测我们选择的 这些功能的神经认知指数将揭示异常神经和计算的独特模式 与健康、年龄和性别匹配的对照组进行比较。我们认为，这些地区的多样性 研究，例如使用多个神经系统，使我们能够解决基础、转换和应用 问题，包括大脑、计算和行为的交叉点的问题。我们的长期目标将是 找出这种交叉研究模式是否有助于开发更有针对性和更高效的 儿童NST的化疗，以及认知障碍的后续护理。通过识别这样的 神经认知表型，这项研究将有助于发展未来的研究和资助战略，旨在 减少化疗的不良反应以及针对特定认知的量身定做的治疗干预 这一群体的概况。