METALIQ: Evaluation of the Humoral and Tumoral Molecular Alteration Profile of Brain Metastases

Sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05848050
Collaborator
(none)
30
1
16.1

Study Details

Study Description

Brief Summary

The purpose of the study is to determine in brain metastases and according to feasibility in liquid biopsies:

  • Molecular alterations including in particular mutations, amplifications, Copy number gene variants and fusion transcripts identified by high-throughput sequencing;

  • The rate of variation either in gain or in loss of expression of the different messenger Ribonucleic Acids by analysis of the transcriptome;

  • Epigenetic alterations by methylation of deoxyribonucleic acid clusters by methylome chips.

Condition or Disease Intervention/Treatment Phase
  • Procedure: biological samples (blood test and lumbar puncture)
N/A

Detailed Description

This is a single-center, prospective, interventional, exploratory study aimed at comparing the molecular alteration profile of liquid biopsies (blood and lumbar puncture) to that of brain metastases.

The population eligible for the study will consist of any patient with cerebral metastases from a solid cancer, at least one of which is accessible to surgical excision.

The study consists of comparing, between brain metastases and liquid biopsies (blood and lumbar puncture), the profiles of genomic, post-genomic and epigenetic alterations as well as the mutational load. To do this, the study only requires a lumbar puncture and a blood test.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
monocentric, prospective, interventional, exploratory studymonocentric, prospective, interventional, exploratory study
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Evaluation of the Humoral and Tumoral Molecular Alteration Profile of Brain Metastases
Anticipated Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: brain metastases from solid cancer

Excision of the cerebral metastasis

Procedure: biological samples (blood test and lumbar puncture)
On the day of excision of the cerebral metastasis, additional biological samples (blood test and lumbar puncture) will be taken in the operating room. A biological sample of the tumor tissue (brain metastases of a solid cancer with contrast uptake of at least 1 cm accessible to surgical excision) will also be taken and preserved by freezing, in accordance with current practice and after obtaining their written agreement. . Biological samples (liquid biopsies and tumour) from patients who have explicitly expressed their consent will be kept after the end of the research as part of a biobank in order to be able to carry out any additional analyses.

Outcome Measures

Primary Outcome Measures

  1. molecular alteration profile of liquid biopsies [1 day]

    Compare the molecular alteration profile of liquid biopsies (blood and CSF) to that of brain metastases. Will be determined in brain metastases and according to feasibility in liquid biopsies (blood and CSF): Molecular alterations including in particular mutations, amplifications, Copy number gene variants and fusion transcripts identified by high-throughput sequencing ; The rate of variation either in gain or in loss of expression of the different messenger Ribonucleic Acids by analysis of the transcriptome ; Epigenetic alterations by methylation of deoxyribonucleic acid clusters by methylome chips.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient aged 18 or over;

  • Patient with cerebral metastases from a solid cancer, at least one of which is accessible to surgical excision (contrast enhancement of at least 1 cm);

  • Patient able to understand the information related to the study and to read the information leaflet;

  • Patient having signed a written informed consent to participate in the study.

Exclusion Criteria:
  • Patient with a medical contraindication to surgery and anesthesia;

  • Patient whose anatomical location of the cerebral metastasis contraindicates wide resection;

  • Patient with a contraindication to performing a lumbar puncture;

  • Pregnant, parturient or breastfeeding women;

  • Patient participating in another clinical trial, or in a period of exclusion from another clinical trial;

  • Patient under guardianship or curatorship, or under a regime of deprivation of liberty;

  • Patient not benefiting from a social security scheme.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • GCS Ramsay Santé pour l'Enseignement et la Recherche

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
GCS Ramsay Santé pour l'Enseignement et la Recherche
ClinicalTrials.gov Identifier:
NCT05848050
Other Study ID Numbers:
  • 2022-A02785-38
First Posted:
May 8, 2023
Last Update Posted:
May 8, 2023
Last Verified:
Apr 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 May 8, 2023