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MRS of Glioma Genomics (GLIOMRS)

Primary Purpose

Glioma

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
MRI
Sponsored by
Institut National de la Santé Et de la Recherche Médicale, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Glioma focused on measuring Gliomas, Isocitrate dehydrogenase, 1p19q codeletion, MR Spectroscopy, MRI, Diagnosis, Treatment monitoring

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Affiliation à un régime de sécurité sociale (bénéficiaire ou ayant droit) Recueil du consentement écrit et éclairé Une des deux situations suivantes : Groupe 1 : Probable gliome de grade II/III, dont l'exérèse est programmée Groupe 2 : gliome de grade II ou III prouvé histologiquement avec statut IDH1/IDH2 connu, n'ayant reçu aucun autre traitement que la chirurgie, et devant débuter un traitement autre que la chirurgie. Présence d'un résidu tumoral évaluable (>2 cm de diamètre en FLAIR) Index de Karnofsky > 60 Contraception efficace pendant la durée de la recherche, complété par un test de grossesse négatif pour les femmes en âge de procréer. Exclusion Criteria: Contrindications à l'IRM: pace maker ou stimulateur neuronal, corps étranger métallique intraoculaire ou intracérébral, implant cochléaire, valve cardiaque ou matériel artériel chirurgical métallique non compatible IRM, matériel métallique susceptible de concentrer les impulsions de radio fréquence, claustrophobie femmes enceintes ou allaitantes Critères réglementaires : Femme enceinte, parturiente, allaitante; Absence de signature du consentement ou refus du participant; Mesure de protection juridique (tutelle, curatelle, sauvegarde de justice); Participation à une autre recherche ne permettant pas de respecter la période; d'exclusion entre les 2 recherches; Personne ne bénéficiant pas d'un régime d'assurance maladie

Sites / Locations

  • Pitié-Salpetrière Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MRI examination

Arm Description

Outcomes

Primary Outcome Measures

Metabolite concentrations by MRS
Concentrations of 2-hydroxyglutarate and cystahionine measured by MRS will be correlated with IDH mutational status and 1p19q codeletion derived from ex vivo analyses in tumor tissue samples

Secondary Outcome Measures

Diffusion MRI metrics
Diffusion MRI metrics will be correlated with the 1p19q codeletion status derived from ex vivo analyses in tumor tissue samples
Metabolic changes during an anti-tumor treatment
The changes in concentration of 2-hydroxyglutarate, cystathionine and choline will be compared to the changes in tumor volumes and to the clinical response
Diffusion MRI and amide proton transfer signal changes during an anti-tumor treatment.
Diffusion MRI and amide proton transfer signal changes will be compared to the changes in metabolism, tumor volumes and to the clinical response

Full Information

First Posted
January 17, 2023
Last Updated
January 27, 2023
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
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1. Study Identification

Unique Protocol Identification Number
NCT05700071
Brief Title
MRS of Glioma Genomics
Acronym
GLIOMRS
Official Title
Magnetic Resonance Spectroscopy Markers of Glioma Genomics
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
February 15, 2023 (Anticipated)
Primary Completion Date
November 24, 2026 (Anticipated)
Study Completion Date
November 24, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut National de la Santé Et de la Recherche Médicale, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In France, about 5000 new people with a primary malignant brain tumor are diagnosed each year. The most common primary tumors are gliomas, originating from glial cells (astrocytomas and oligodendrogliomas). Low-grade gliomas are mildly aggressive, but they often evolve into a more malignant form. Mutations in the genes encoding isocitrate dehydrogenase (IDH) are found in about 80% of low-grade gliomas and are associated with a favorable prognosis. Remarkably, IDH-mutated gliomas are characterized by a specific cellular metabolism causing the accumulation of D-2-hydroxyglutarate (2HG) in tumor cells. 2HG can be detected in vivo using 1H magnetic resonance spectroscopy (MRS) and is recognized as a unique, noninvasive biomarker of IDH-mutated gliomas. Noninvasive detection of IDH mutations via 2HG MRS represents a crucial step for decision-making and patient care. A subset of IDH-mutated tumors also presents a complete deletion of 1p and 19q chromosome arms (1p/19q codeletion). The 1p/19q codeletion is specifically linked to the oligodendroglial histologic subtype and it has been associated with a better patient outcome. However, the biological effects of this genetic alteration are still unclear and in vivo markers are lacking. Recently, we reported the first in vivo detection of the cystathionine molecule in human brain gliomas using MRS and explored the association between cystathionine accumulation and 1p/19q codeletion in gliomas. In this project, the investigation team will combine cutting edge MRI and MRS techniques for metabolic and microstructural characterization of brain tumors with the aim of providing novel reliable noninvasive biomarkers of tumor genetic subtypes. These methods will enable noninvasive identification of IDH-mutated gliomas and, potentially, 1p/19q codeleted gliomas. In addition, the researchers will investigate the utility of 2HG, cystathionine and MRI microstructural markers to monitor tumor response to anti-cancer treatments and tumor progression. The outputs of this project, altogether, may open new avenues to a better understanding of the pathophysiological mechanisms of oncogenesis and the design of new treatments for gliomas.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioma
Keywords
Gliomas, Isocitrate dehydrogenase, 1p19q codeletion, MR Spectroscopy, MRI, Diagnosis, Treatment monitoring

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MRI examination
Arm Type
Experimental
Intervention Type
Diagnostic Test
Intervention Name(s)
MRI
Intervention Description
MRI without contrast agent
Primary Outcome Measure Information:
Title
Metabolite concentrations by MRS
Description
Concentrations of 2-hydroxyglutarate and cystahionine measured by MRS will be correlated with IDH mutational status and 1p19q codeletion derived from ex vivo analyses in tumor tissue samples
Time Frame
1.5 hour
Secondary Outcome Measure Information:
Title
Diffusion MRI metrics
Description
Diffusion MRI metrics will be correlated with the 1p19q codeletion status derived from ex vivo analyses in tumor tissue samples
Time Frame
1,5 hours
Title
Metabolic changes during an anti-tumor treatment
Description
The changes in concentration of 2-hydroxyglutarate, cystathionine and choline will be compared to the changes in tumor volumes and to the clinical response
Time Frame
1 year
Title
Diffusion MRI and amide proton transfer signal changes during an anti-tumor treatment.
Description
Diffusion MRI and amide proton transfer signal changes will be compared to the changes in metabolism, tumor volumes and to the clinical response
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Affiliation à un régime de sécurité sociale (bénéficiaire ou ayant droit) Recueil du consentement écrit et éclairé Une des deux situations suivantes : Groupe 1 : Probable gliome de grade II/III, dont l'exérèse est programmée Groupe 2 : gliome de grade II ou III prouvé histologiquement avec statut IDH1/IDH2 connu, n'ayant reçu aucun autre traitement que la chirurgie, et devant débuter un traitement autre que la chirurgie. Présence d'un résidu tumoral évaluable (>2 cm de diamètre en FLAIR) Index de Karnofsky > 60 Contraception efficace pendant la durée de la recherche, complété par un test de grossesse négatif pour les femmes en âge de procréer. Exclusion Criteria: Contrindications à l'IRM: pace maker ou stimulateur neuronal, corps étranger métallique intraoculaire ou intracérébral, implant cochléaire, valve cardiaque ou matériel artériel chirurgical métallique non compatible IRM, matériel métallique susceptible de concentrer les impulsions de radio fréquence, claustrophobie femmes enceintes ou allaitantes Critères réglementaires : Femme enceinte, parturiente, allaitante; Absence de signature du consentement ou refus du participant; Mesure de protection juridique (tutelle, curatelle, sauvegarde de justice); Participation à une autre recherche ne permettant pas de respecter la période; d'exclusion entre les 2 recherches; Personne ne bénéficiant pas d'un régime d'assurance maladie
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marc Sanson, MD, PhD
Phone
(0)1 42 16 03 91
Ext
0033
Email
marc.sanson@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Francesca Branzoli, PhD
Phone
(0)1 57 27 46 46
Ext
0033
Email
francesca.branzoli@icm-institute.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesca Branzoli, PhD
Organizational Affiliation
Paris Brain Institute, Paris, France
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Marc Sanson, MD, PhD
Organizational Affiliation
Paris Brain Institute, AP-HP, Paris, France
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pitié-Salpetrière Hospital
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marc Sanson, MD, PhD
Phone
(0)1 42 16 03 91
Ext
0033
Email
marc.sanson@aphp.fr

12. IPD Sharing Statement

Plan to Share IPD
No

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MRS of Glioma Genomics

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