GLIOMANOID: Organoids Derived From Induced-Pluripotent Stem Cells (iPS) From Patients With High Grade Astrocytoma

Sponsor
Assistance Publique Hopitaux De Marseille (Other)
Overall Status
Unknown status
CT.gov ID
NCT03971812
Collaborator
(none)
20
1
18
1.1

Study Details

Study Description

Brief Summary

The objective of this study research proposal is to model human gliomagenesis using 3-Dimensional (3D) brain organoids derived from human induced pluripotent stem cells (hiPSCs).

The working hypothesis is that 3D brain organoids can develop glioma-like structures and recapitulate phenotypic traits of gliomas when generated from hiPSCs expressing genetic mutants associated with glioma predisposition.

Methodology : To develop this pioneer study on the use of hiPSC-based brain organoids as a strategy to model gliomagenesis and study the impact of genetic mutants, it will be collect the peripheral blood mononuclear cell from 20 patients with high grade astrocytoma with or without IDH mutation. iPS will be generated from these PBMC and will be genetically modified according to different mutations. Then, it will be generate brain organoids according to standard protocols. Brain organoids generated from all different cells will be collected at different time points and analyzed for the presence of glioma-like structures and phenotypic hallmarks of gliomas.

From the proposed experiments, it will be expect that brain organoids will develop glioma-like features upon the presence of genetic mutations. Thus, it will be expect to demonstrate that brain organoids can be used as a reliable strategy to test the impact of genetic mutants, including the possible synergistic cooperation between different mutations on early gliomagenic events.

Condition or Disease Intervention/Treatment Phase
  • Biological: Blood sample

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Organoids Derived From Induced-Pluripotent Stem Cells (iPS) From Patients
Anticipated Study Start Date :
Jun 7, 2019
Anticipated Primary Completion Date :
Dec 6, 2020
Anticipated Study Completion Date :
Dec 6, 2020

Arms and Interventions

Arm Intervention/Treatment
Patient with high grade astrocytoma

Patients meeting inclusion and non-inclusion criteria and having signed informed consent will be included in the study

Biological: Blood sample
A blood sample of two 10 mL ethylenediaminetetraacetic (EDTA) tubes will be taken at the time of the visit. This sample will be centrifuged for isolation of peripheral blood mononuclear cells (PBMC).

Outcome Measures

Primary Outcome Measures

  1. Characterize the level of proliferation of organoids [18 months]

    compare different immunohistochemical markings between organoids

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient, male or female, aged 18 years or older

  • Astrocytoma grades 3 or 4, confirmed by anatomopathological diagnosis

  • Patient having signed an informed consent

Exclusion Criteria:
  • Person in emergency situation, a legal person of legal age (guardianship, guardianship or legal guardianship), or unable to express his / her consent

  • No affiliation to a social security scheme (beneficiary or beneficiary)

  • Pregnant or lactating woman

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assistance Publique Hôpitaux de Marseille Marseille France 13354

Sponsors and Collaborators

  • Assistance Publique Hopitaux De Marseille

Investigators

  • Study Director: Jean-Olivier ARNAUD, Director, Assistance Publique Hôpitaux de Marseille

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique Hopitaux De Marseille
ClinicalTrials.gov Identifier:
NCT03971812
Other Study ID Numbers:
  • 2019-01
  • 2019-A00145-52
  • RCAPHM19_0001
First Posted:
Jun 3, 2019
Last Update Posted:
Jun 13, 2019
Last Verified:
Jun 1, 2019
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

Study Results

No Results Posted as of Jun 13, 2019