The 2007 WHO classification of tumours of the central nervous system.
David N Louis, Hiroko Ohgaki, Otmar D Wiestler...
https://pubmed.ncbi.nlm.nih.gov/17618441Actively Recruiting
Led by Institut du Cancer de Montpellier - Val d'Aurelle · Updated on 2025-02-12
1700
Participants Needed
1
Research Sites
208 weeks
Total Duration
Primary central nervous system tumors (PCNST) include various types of tumors affecting the brain, spinal cord, meninges, and nerves. These tumors can be benign, malignant, or borderline and have over 140 subtypes with different causes, prognoses, and treatments. Due to their rarity and diversity, there is limited knowledge about many PCNST subtypes, making the creation of a comprehensive clinical database important for research on tumor characteristics, treatment impact, and survival outcomes. This study involves collecting detailed clinical, radiological, and biological data from patients with PCNST treated at the Montpellier Cancer Institute. It includes both retrospective data from patients treated since 2004 and prospective data from ongoing patients. The database will gather information on tumor diagnosis, treatments received, and follow-up until death or progression, aiming to support clinical and epidemiological studies and facilitate patient identification for future research. Participants in this observational study provide information through their medical records and questionnaires. Researchers will track outcomes such as tumor progression and survival for up to 100 months after inclusion. The study collects data systematically to analyze predictive factors and prognosis across different tumor subtypes. Participation involves data sharing, and patients' clinical course is monitored over time without altering their standard care.
CONDITIONS
Creation of a Clinical Database on Primary Nervous System Tumors
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - From date of inclusion until the date of first documented progression or death, assessed up to 100 months
Participants have diagnostic data collected including symptoms, radiological and histological diagnosis, tumor characteristics, and molecular data.
Data collected from medical records; visit frequency varies
Duration - From date of inclusion until the date of first documented progression or death, assessed up to 100 months
Participants are followed over time to observe treatment sequences, oncological treatments, toxicities, and survival outcomes.
Data collection occurs throughout treatment and follow-up; visit frequency varies
Total: 1 location
1
Icm Val D'Aurelle
Montpellier, Herault, France, 34298
Actively Recruiting
A
Aurore MOUSSION, MD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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