ExoGLIE: Clinical Relevance of Detecting Molecular Abnormalities in Glial Tumor Exosomes

Sponsor
University Hospital, Limoges (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06116903
Collaborator
(none)
60
1
24

Study Details

Study Description

Brief Summary

The purpose of this pilot study is that exosomes constitute a more interesting support for analyzes allowing a broader screening of molecular alterations to be carried out with more reliable, more sensitive and more efficient results than the reference Foundation One Liquid CDx test.

Condition or Disease Intervention/Treatment Phase
  • Genetic: Blood sampling
N/A

Detailed Description

Gliomas are the most common primary brain tumors in adults. The heterogeneity of tumors, the lack of reliable criteria for identifying different subtypes make their histopathological diagnosis and their management complex. The molecular profiling from circulating exosomes is one of the most promising approaches to better characterize gliomas.

We will demonstrate the superiority of detection by NGS of molecular abnormalities present in exosomes from glioblastomas, compared to detection by the Foundation One Liquid CDx test on ctDNA.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Clinical Relevance of Detecting Molecular Abnormalities in Glial Tumor Exosomes
Anticipated Study Start Date :
Dec 15, 2023
Anticipated Primary Completion Date :
May 15, 2025
Anticipated Study Completion Date :
Dec 15, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Detection of molecular abnormalities

Blood samples will be taken from 2 + 3 Cell-Free DNA Collection tubes (Roche): for the comparative performance of the two methods (main objective) 3 Cell-Free DNA Collection tubes will be collected at 3 months (post chemotherapy) to evaluate the clinical relevance of a new analysis of molecular alterations on exosomes

Genetic: Blood sampling
Blood sampling for testing of the detection of molecular abnormalities in exosomes of glial tumors

Outcome Measures

Primary Outcome Measures

  1. Analyse Next-generation sequencing (NGS) [3 months]

    Higher proportion of contributory samples identified by NGS analysis (via exosomes) compared to that of FMI (Foundation Medicine International) test (at inclusion)

Secondary Outcome Measures

  1. Expression of biomarkers [3 months]

    Level of expression of biomarkers, for the same patient, by molecular analysis of exosomes and blood sampling according to the FMI test protocol

  2. Molecular alterations [3 months]

    Modification or not modification of the profile of the molecular alterations

  3. carbon footprint [3 months]

    Evaluation of the carbon footprint for each of the 2 techniques (NGS via exosomes and FMI test)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subject of both sexes at least 18 years of age with glioblastoma.

  • Patient for whom an FMI test is indicated, progressing after a 1st line following the chemotherapy and radiotherapy protocol (STUPP protocol)

  • Patient affiliated to French social security

Exclusion Criteria:
  • Patient included in another research protocol using an experimental molecule.

  • Any medical or psychiatric condition which, in the Investigator's opinion, would preclude the patient from adhering to the protocol or completing the study per protocol

  • Patient under legal protection, guardianship or curatorship

  • Patient with active malignancy or a previous malignancy within the past 5 years; except for patient with resected Basocarcinoma and resected carcinoma in-situ of the cervix.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Hospital, Limoges

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Limoges
ClinicalTrials.gov Identifier:
NCT06116903
Other Study ID Numbers:
  • 87RI22_0011-ExoGLIE
First Posted:
Nov 3, 2023
Last Update Posted:
Nov 3, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 3, 2023