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临床试验/NCT05082961
NCT05082961招募中不适用

Circulating Immunes Cells, Cytokines and Brain Radiotherapy

Centre Francois Baclesse2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年1月27日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40
试验地点
2
主要终点
CD8+ T-cell count.

研究概览

简要总结

Patients with malignant tumours of the cephalic pole have a poor prognosis, despite a wide range of treatments. prognosis despite a large therapeutic arsenal. Among this arsenal, radiotherapy (RT) is one of the standard treatments for these tumours. However, this treatment can cause damage to the surrounding healthy tissue, has limited efficacy in hypoxic However, this treatment can cause damage to the surrounding healthy tissue, has limited efficacy in hypoxic tissue and can promote pro-tumour inflammation.

In these circumstances, hadrontherapy, which uses charged heavy particles, such as protons or carbon ions, is the preferred treatment. protons or carbon ions, seems more appropriate for the treatment of these tumours. However, although inflammation plays a major role in tumour development and tumour development and therapeutic response, few studies have evaluated the immune response response after proton therapy (PT) and carbon therapy (CT). The objective of this project is to study the effect of hadrontherapy on resident/circulating inflammation after brain irradiation. brain irradiation. In a first step, the impact of different PT and CT TEL on macrophages (MФ), the most abundant immune cells in malignant solid tumours, will be evaluated in vitro. malignant solid tumours, will be evaluated in vitro. In a second step, the evolution of circulating leukocytes after brain irradiation with X-rays or protons will be studied in vivo in rodents and patients. rodent and patient. In this project, we propose to study for the first time the inflammatory response after hadrontherapy in the context of a cephalic tumour. cephalic tumour. These results will allow a better understanding of the biological response response following PT and CT with the aim of optimising RT and potentially and potentially translate these data to the clinic.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Participant)

入排标准

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

入选标准

  • Patients > 18 years
  • Head and neck cancer: (upper aerodigestive tract, cavum, facial sinus, skull base, brain) operated
  • Surgery for complete tumour resection or with microscopic residue R1
  • All possible histologies: squamous cell carcinoma, undifferentiated carcinoma of the nasopharyngeal type (UCNT), adenocarcinoma, adenoid cystic carcinoma, chordoma, chondrosarcoma,meningioma other tumours
  • Patients undergoing exclusive postoperative radiotherapy with a minimum total dose of 54 Gy of X-ray photon radiation or equivalent proton radiation.
  • Patient affiliated to a social security scheme
  • Signature of the informed consent before any specific procedure related to the study

排除标准

  • Macroscopic postoperative tumour residue R2
  • Previous cancer within 5 years (except treated basal cell skin carcinoma and treated cervical cancer).
  • Previous radiotherapy (except brachytherapy of the cervix or prostate)
  • Chemotherapy or other systemic oncological treatment (cetuximab) concomitant with radiotherapy
  • Long-term immunosuppressive or corticosteroid therapy
  • Patient deprived of liberty or under guardianship, protected adult
  • Patient unable to undergo trial monitoring for geographical, social or psychopathological reasons
  • Pregnant or breastfeeding woman
  • Emergency situations

结局指标

主要结局

CD8+ T-cell count.

时间窗: up to 3 months

次要结局

  • CD4+ Lymphocytes T count(up to 3 months)
  • Regulatory T cells(up to 3 months)

研究者

发起方
Centre Francois Baclesse
申办方类型
Other
责任方
Sponsor

研究点 (2)

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