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临床试验/NCT02309242
NCT02309242Unknown不适用

Long Term Neurotoxic Effects of Chemotherapy in Survivors of Bone and Soft Tissue Sarcomas. A Retrospective Study

Universitaire Ziekenhuizen KU Leuven1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2014年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
60
试验地点
1
主要终点
Neuropsychological functioning

研究概览

简要总结

The aim of the proposed project is to study the long-term impact of adjuvant systemic multi- agent chemotherapy (cisplatin, anthracyclines, vincristine, methotrexate, alkylating agents) in survivors (treated between 1992 and 2014 in UZ Leuven) of paediatric bone or soft tissue sarcomas on neurocognitive functioning.

详细描述

The aim of the proposed project is to study the long-term impact of adjuvant systemic multi- agent chemotherapy (cisplatin, anthracyclines, vincristine, methotrexate, alkylating agents) in survivors (treated between 1992 and 2014 in UZ Leuven) of paediatric bone or soft tissue sarcomas on neurocognitive functioning using neuropsychological testing in combination with advanced Magnetic Resonance (MR) imaging techniques in a cross-sectional design. The majority of studies focus on either neuropsychological outcomes or structural imaging. In this project we want to combine both methodologies. MR will mainly focus on microstructural changes in white matter and differences in brain connectivity, while with our neuropsychological tests we will assess a broad range of cognitive functioning. From the obtained MR parameters and neuropsychological test results, the proposed study wants to answer the following research questions:

  1. Are there subtle differences in neurocognitive function and behavior related to chemotherapy exposure for survivors of paediatric bone or soft tissue sarcomas?
  2. Are there differences in morphological/functional MR parameters that could relate to subtle cognitive differences in cognitive functioning after chemotherapy exposure? Can we detect structural treatment-induced WM injury? Can we see differences in brain neural activity/connectivity during rest between the groups?
  3. Is there a correlation between the obtained morphological/functional MR parameters and neuropsychological test results?
  4. Is there a correlation between the possible difference in white matter microstructure and gender, age at diagnosis and the duration of treatment?

To answer these questions, we will implement the following measurements:

  • From the computerized Amsterdam Neuropsychological Tasks (ANT) system we will test simple motor reaction time, sustained, focused and divided attention, inhibitory control and cognitive flexibility and motor coordination.
  • Specific verbal-auditory memory and nonverbal, visual-spatial memory functioning will be registered by the Children's Memory Scale (CMS) for subjects younger than 16 years and with the auditory verbal learning test and the Rey visual design learning test for the subjects older than 16 years. Age-adjusted standardized norms are available for each test.
  • The BRIEF (Behavior Rating Inventory of Executive Function) explores executive functioning in school (5-17 years), work (+18 years) and home (5-17 years and +18 years) environments.
  • The assessment of intellectual functioning consists of the Wechsler Intelligence Scale for Children (WISC-III) for patients between 6 and 16 years and the Wechsler Adult Intelligence (WAIS-III) for adolescents aged 17 years or older.
  • Quality of life will be investigated by the PEDSQL generic version for young adults .
  • The Achenbach questionnaires (Child Behavior Checklist, Teacher Report Form, Youth Self Report Form, Adult Behavior Checklist, Adult Self Report Form) items for internalizing, externalizing, and total problems will be filled out by the parents, teacher or relatives and patients themselves.
  • All participants will complete the Spielberger State-Trait Anxiety Inventory and the Beck Depression Inventory-II.

Currently, the neurocognitive follow-up of paediatric bone and brain tumour patients (NKP21/22c, National Cancer Plan Onkelinx) as well as children with congenital heart disease (IWT-TBM, 3M110068) or treated in a paediatric intensive care unit is also based on this test battery. All these tests and questionnaires have been extensively described and used to quantify neurocognitive development and Quality of life in various paediatric populations. The testing will be performed at least one year after the end of treatment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Screening
盲法
None

入排标准

年龄范围
7 Years 至 25 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Survivors of paediatric bone or soft tissue sarcomas, who were treated from 1992 onwards in the paediatric haematooncology department of UZLeuven according to one of the following treatment protocols.
  • •*For soft tissue sarcomas: MMT 95, MMT 98, RMS2005 or NRST2005
  • •*For Ewing sarcoma: EICESS 92, Euro-Ewing 99 or Euro-Ewing 2008
  • •*For osteosarcoma: EORTC 80931 or Euramos1 protocols
  • •There will be variability in treatment regimens, but the patient group will be clustered into four subgroups:
  • •Cisplatin and anthracyclines
  • •Cisplatin, anthracyclines and methotrexate
  • •Alkylating agents
  • •Alkylating agents and anthracyclines

排除标准

  • •Mental retardation documented before treatment
  • •Inability to perform the tests because of motor or sensory deficits
  • •Other cognitive disorders
  • •Depression
  • •Parameningeal or intracranial sarcomas
  • •Syndrome (e.g. Down)
  • •Autologous stemcell transplantation
  • •Head/neck/spinal radiotherapy or psychopharmaca

研究组 & 干预措施

Neuropsychological assessment, MRI

No Intervention

This is a cross-sectional mono-center study examining survivors who were exposed to chemotherapy for bone or soft tissue sarcomas in childhood. Survivors of bone or soft tissue sarcomas will be examined with neuropsychological tests, questionnaires and advanced MR imaging (Neuropsychological assessment, MRI). Results will be compared to a healthy control group matched for age and sex.

干预措施: Neuropsychological assessment, MRI (Behavioral)

结局指标

主要结局

Neuropsychological functioning

时间窗: 4 years

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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