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临床试验/NCT03977896
NCT03977896已完成不适用

Pilot Study to Evaluate the Feasibility of Hybrid Brain Imaging 11C-MET PET/MRI of Posterior Brain Fossa Tumors in Children

Hospices Civils de Lyon2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2019年11月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
15
试验地点
2
主要终点
number of patients called in for PET/MRI who have not realized the PET/MRI

研究概览

简要总结

Brain tumors are the most common solid tumors in children and are the second most common cause of cancer-related death among this population. Posterior brain fossa tumors represent about 50% of children brain tumors.

Recently, knowledge in molecular biology has permitted to identify different tumors subgroups of very different prognosis. Today, surgery removal of the tumor is the mandatory. Neuro-oncological treatment differs depending on the histological and molecular subgroup. With classical Magnetic Resonance Imaging (cMRI), distinction between different types of posterior fossa tumors remains difficult.

Positron Emission Tomography combined with MRI (PET/MRI) has proven its benefits for the management of brain tumors. The direct spatiotemporal correlation makes possible the assessment of metabolic, anatomical and functional information. PET/MRI would provide precisions on the pre-therapeutic characterization of tumors, which could permit to modify the patients' care.

L- [methyl-11C] methionine (11C-MET) is currently the gold-standard tracer used in neuro-oncology, but few data exists in children. 11C-MET PET/MRI assessment seems promising, but has not been studied enough. To the best of our knowledge, there is no specific study on primary brain tumors of the posterior fossa in children using 11C-MET PET/MRI.

The primary objectives of this first pilot study is to evaluate the practical feasibility of 11C-MET PET/MRI imaging (machine accessibility and imaging interpretability) before surgery in a population of children older than 5 years old with posterior fossa tumors.

The secondary objectives aim to describe :

  • the PET/MRI parameters of the different tumors studied,
  • and the patient's participation acceptation.

This feasibility study will allow us to standardize the PET/MRI measurements; this could allow us to discriminate, in a larger study, the different tumor subgroups before surgery.

研究设计

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

入排标准

年龄范围
5 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patients ≥ 5 years old and < 18 years old at enrollment,
  • with primary posterior brain fossa tumor, metastatic or not,
  • hospitalized in the Department of Pediatric Neurosurgery of Femme-Mère-Enfant Hospital, and for whom a surgery is scheduled,
  • covered by national health insurance,
  • patient's parents or legal guardians who have provided written informed consent prior to participation in the study.

排除标准

  • Patients with contraindication for MRI (claustrophobia, carrying metallic object)
  • Patients with contraindication for Gadolinium injection (including pregnancy and breastfeeding)
  • patient with recurring posterior brain fossa tumor
  • patient with brain stem infiltrative tumor

结局指标

主要结局

number of patients called in for PET/MRI who have not realized the PET/MRI

时间窗: 7 days

number of patients who performed the PET/MRI

时间窗: 7 days

number of patients with good quality of the imaging

时间窗: 7 days

The interpretability of the imaging will be evaluated by a Review Committee (two pairs composed each by a radiologist (for MRI imaging) and a nuclear physician (for PET imaging)). The imaging will be classified under good or bad quality

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 (2)

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