Molecular Heterogeneity in Multilobar Low-grade Gliomas

NCT ID: NCT04000048

Last Updated: 2019-12-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

8 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-06-24

Study Completion Date

2020-12-31

Brief Summary

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Low-grade diffuse glioma (GDBG) are rare tumors of young adults, whose ontogenesis is poorly understood. Patient management is based on the molecular profile defined by two molecular markers : mutations of the IDH genes and chromosomal 1p19q co-deletion. To date, the IDH and 1p19q statuses are determined on a single fragment collected from the tumor. In the case of GDBGs infiltrating several brain lobes, the sampling is done randomly on only one of the infiltrated lobes. An intra-tumoral heterogeneity of genetic alterations has been suggested and would impact management.

Phylogenetic analysis of genetic alterations found, by high throughput sequencing, in each lobe invaded by the same GDBG will make it possible to assess intra-tumoral heterogeneity and to discuss, at a fundamental level, the hypothesis of a single tumor site with secondary diffusion or that of the convergent progression of two or three distinct tumor sites. Clinically, understanding the ontogenesis of GDBGs will improve their management because of the known link between brain location, dominant molecular profile, and prognosis.

Detailed Description

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Conditions

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Low-grade Diffuse Glioma

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

OTHER

Interventions

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sequencing of the complete exome

Once the pathological diagnosis is confirmed (WHO 2016), a tumor fragment will be selected and frozen for each lobe. DNA extraction will be performed for each fragment. The samples (4 different DNAs per GDBG corresponding to the DNA extracted from each of the 3 lobes and the blood DNA) will be sent to the Montpellier Genomix platform for sequencing of the complete exome.

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

* Be over 18 years old.
* Subject not opposed to participating in the study
* Be scheduled in the operating room for the first surgery of a low-grade diffuse glioma presupposition on the basis of clinical and imaging criteria.
* Confirmation, after histopathological analysis of the resected tumor fragments, of the diagnosis of grade II glioma according to the 2016 WHO classification of brain tumors.

Exclusion Criteria

* Patient minor, or major under legal protection, or unable to give consent.
* Refusal to participate in the study.
* Pathology diagnosis of grade III glioma according to WHO 2016 classification
* Have received oncology treatment (chemotherapy and or chemotherapy) before the first surgery.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Montpellier

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU Gui de Chauliac

Montpellier, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Catherine Gozé, PharmD, PhD

Role: CONTACT

0467335872

Facility Contacts

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Catherine GOZE, Pharm-D; PhD

Role: primary

0467335872

Hugues DUFFAU, PU-PH

Role: backup

Other Identifiers

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RECHMPL18_0376

Identifier Type: -

Identifier Source: org_study_id

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