Glioma Clinical Trial
Official title:
Non Invasive IDentification of Gliomas With IDH1/2 Mutation by Analysis of Circulating Plasmatic DNA, D-2-hydroxyglutarate Dosage in Biological Liquids and Detection by Brain SPEctro-MRI: Impact for Diagnosis and Follow-up
This trial develops a non invasive diagnostic approach of IDH1 mutated gliomas combining
mutation detection from free plasmatic DNA, D-2HG dosage in urine samples, and D-2HG
detection by Brain Spectro MRI.
In group 1 (25 patients), patients with presumed grade II-III gliomas candidate to surgery
will undergo spectro MRI, plasma, urine dosages. Results will then be confronted to tumor
mutational status and D-2HG.
In group 2 (15 patients), patients with known IDH1 mutation will undergo spectro MRI, plasma,
urine dosages overtime in order to correlate results with the response to treatment.
The aim of this trial is to develop and validate a non invasive diagnostic approach of IDH1
mutated gliomas. It will evaluate the specificity and sensitivity of D-2HG detection by Brain
Spectro MRI. This approach will be coupled with mutation detection from free plasmatic DNA
and D-2HG dosage in urine samples.
The primary end-point is the quantification of D-2HG by spectro-MRI, and the correlation with
the dosage of D-2HG in the tumor fragment, and the mutational status (group 1: 25 patients).
The secondary endpoints include:
1. longitudinal analysis Spectro-MRI overtime (12 months) correlation with radiological
evolution and the response to treatment (group 2: 15 patients)
2. Differentiation of tumor recurrence from radiation induced changes
3. Confrontation of Spectro-MRI, D-2HG dosages and IDH mutation detection from plasma DNA,
and elaboration of a combined score of prediction
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