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临床试验/NCT03980977
NCT03980977已完成不适用

Collection of Biological Samples for Stydy of Unusual Toxicity Induced by Radiotherapy

Institut de Cancérologie de Lorraine2 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2018年5月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
45
试验地点
2
主要终点
skin fibroblast radiosensitivity

研究概览

简要总结

In order to evaluate the physiopathological knowledge of the different pathological manifestations associated with individual radiosensitivity, it seems essential to carry out this pilot study. It has agglomerated homogeneous tissue samples to identify new biomarkers for patient diagnosis and follow-up, and may predict the therapeutic response. These knowledge will help to treatment customization.

研究设计

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

入排标准

年龄范围
2 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Child or teenager aged 2 to <18
  • Man, Woman> 18 years old
  • Patient with one of these situations:
  • Unusual toxicity in progress or after radiotherapy
  • Indication of radiotherapy and suspicion of abnormal pathways of response to ionizing radiation - constitutional (genetic disease) or acquired (systemic disease) - which may generate unusual radioinduced toxicity
  • Patient information and informed consent signed by the patient. For children and teenager : information to parents and obtaining informed consent
  • Affiliation to a social security scheme.

排除标准

  • Contraindication for skin and / or tumoral biopsy
  • Contraindication for blood sample of 2.5 ml
  • Persons deprived of liberty or under supervision

结局指标

主要结局

skin fibroblast radiosensitivity

时间窗: 2 to 3 months after skin biopsy

The number of residual double strand break at 24 hours (number of 53BP1 foci) after a dose of 2 Gy will be quantified with indirect immunofluorescence

次要结局

  • tumor cells radiosensitivity(2 to 3 months after tumor biopsy)

研究者

发起方
Institut de Cancérologie de Lorraine
申办方类型
Other
责任方
Sponsor

研究点 (2)

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