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Feasibility of 11C-MET PET/MRI Imaging in Pediatric Brain Fossa Tumors

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03977896
Acronym
TI-TFCE
Enrollment
15
Registered
2019-06-06
Start date
2019-11-03
Completion date
2021-11-08
Last updated
2025-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posterior Brain Fossa Tumors in Children

Keywords

PET/MRI, 11C-MET, posterior brain fossa tumors, children, surgery, feasibility

Brief 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.

Interventions

PROCEDURE11C-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).

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 17 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
number of patients who performed the PET/MRI7 days
number of patients called in for PET/MRI who have not realized the PET/MRI7 days
number of patients with good quality of the imaging7 daysThe 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

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026