Harmonization strategies for multicenter radiomics investigations.
R Da-Ano, D Visvikis, M Hatt
https://pubmed.ncbi.nlm.nih.gov/32688357/Actively Recruiting
Led by Institut Claudius Regaud · Updated on 2026-06-04
370
Participants Needed
1
Research Sites
17 weeks
Total Duration
Ependymoma is the second most common brain tumor in children and adolescents, often treated with surgery and radiation. However, relapses occur in about half of cases, mainly at the original tumor site, due to factors like radio-resistance. Researchers aim to use advanced imaging, molecular biology, and artificial intelligence in the EPENDYMOMICS project to identify characteristics that predict relapse and define new radiotherapy targets, improving treatment strategies for this challenging disease. This project collects extensive clinical, biological, imaging, and radiotherapy data from previous studies and a national database called NETSPARE, involving over 370 children and adolescents treated in France. Researchers analyze multimodal MRI, histopathology, DNA methylation profiles, and other molecular data. They apply deep learning and radiomics techniques to develop predictive signatures that combine imaging and molecular features, aiming to identify radioresistant tumor clusters and improve understanding of relapse mechanisms. Participants data include MRI scans, radiotherapy plans, clinical history, histology slides, and molecular analyses. Researchers perform detailed image processing and harmonization to standardize diverse data. They develop and validate radiogenomic signatures predicting progression-free survival and relapse patterns using large patient cohorts. The study tracks outcomes over 30 months, focusing on radiogenomics markers and potential new radiotherapy target volumes to guide future clinical trials addressing radioresistance in pediatric ependymoma.
CONDITIONS
Multiomic Approach to Radioresistance of Ependymomas in Children and Adolescents
A
Anne LAPRIE, PU-PH
F
Fatima TENSAOUTI, phD
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Institut Claudius Regaud
Lead Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Collaborating Sponsor
You may qualify if you...
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 30 months
Participants provide existing clinical, imaging, radiotherapy, histology, and molecular biology data related to intracranial ependymoma for analysis.
Data collection from existing records and images; no specific visits required
Duration - Up to 30 months
Participants' data are used to analyze prognostic factors, radioresistance, and develop radiogenomics signatures predictive of outcomes.
No active visits; ongoing data analysis and follow-up using existing data
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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https://pubmed.ncbi.nlm.nih.gov/29500084/Institut Claudius Regaud
Lead Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Collaborating Sponsor