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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03977896
Other study ID # 69HCL18_0867
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 3, 2019
Est. completion date November 8, 2021

Study information

Verified date November 2021
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date November 8, 2021
Est. primary completion date November 8, 2021
Accepts healthy volunteers No
Gender All
Age group 5 Years to 17 Years
Eligibility Inclusion Criteria: - 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. Exclusion Criteria: - 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

Study Design


Related Conditions & MeSH terms

  • Neoplasms
  • Posterior Brain Fossa Tumors in Children

Intervention

Procedure:
11C-MET PET/MRI
Except PET/MRI imaging, all the examinations will be done according to the patient's usual care. PET/MRI imaging will be realized within max 7 days after children enrollment, and the surgery (usual care) will be performed within max 4 days after PET/MRI imaging. PET/MRI imaging will include the following sequences: T1axial, Diffusion, Magnetic susceptibility post-Gadolinium injection, 3DT1 pre and post-Gadolinium injection, and Arterial Spin Labelling Imaging (ASL).

Locations

Country Name City State
France Hospices Civils de Lyon - Groupement Hospitalier Est - Hôpital Femme Mère Enfant - Service de Neurochirurgie Pédiatrique Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of patients who performed the PET/MRI 7 days
Primary number of patients called in for PET/MRI who have not realized the PET/MRI 7 days
Primary number of patients with good quality of the imaging 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 7 days