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In Situ Immune Parameters and Their Prognostic Role on the Survival of Patients With Glioblastoma

In Situ Immune Parameters and Their Prognostic Role on the Survival of Patients With Glioblastoma

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03481231
Acronym
IMMUNOGLIO
Enrollment
160
Registered
2018-03-29
Start date
2020-09-13
Completion date
2024-09-14
Last updated
2025-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glioblastoma

Keywords

immunotherapy, tumors and blood samples

Brief summary

Glioblastoma (GBM) is the most frequent brain tumor. Currently survival is poor and few treatments are available. Recent data show that there is no immune privilege of the central nervous system (CNS) and that GBM are invaded by effector CD8 T cells, letting us hypothesis that GBM growth is dependent of immunosurveillance. The aim of this study is to better understand the antitumor immune response against GBM to unravel new effectors and immunosuppressive pathways important for the regulation of anticancer immunity and to discover new immune activating strategies with the objectives to isolate subgroups of GBMs that could benefit from an immunotherapy approach. To achieve this goal, GBM tumor samples and a blood sample will be collected during the initial tumor resection. The sites involved in the recruitment of the patients will be the neurosurgical teams in Brussel, Dijon, Nantes and Padova.

Detailed description

Primary objective : The primary objective is to determine for each of the 3 molecular subtypes of glioblastoma the predictive performance on 1-year overall survival of in situ immune parameters Secondary objectives : To identify the best combination of in vivo immune parameters that is predictive of 1-year overall survival To determine the impact of immune parameters on overall survival Create a collection of biological samples

Interventions

None listed

Sponsors

Centre Georges Francois Leclerc
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Patients with newly diagnosed, brain tumor 2. Gross or near total resection of the contrast-enhancing tumor mass decides by the neurosurgeron. 3. Subjects ≥18 and ≤75 years of age at surgery 4. Patients must be able to understand and sign the informed consent documents indicating that they are aware of the investigational nature of this study. 5. Confirmation of the diagnosis of grade IV GBM by the local pathologist with an independent neuropathologist who will review this diagnosis 6. Primary therapy must consist of surgical resection with the intent for a gross or near total resection of the contrast-enhancing tumor mass, followed by conventional external beam radiation therapy and concurrent temozolomide chemotherapy. 7. Tumor biopsy for biological analysis has to be performed before using ultrasonic surgery

Exclusion criteria

1. Patient with other type of primary brain tumor or metastases 2. Patients with only biopsy performed for the diagnosis 3. Subjects under guardianship, curatorship or judicial protection 4. Female subjects who are pregnant or breast-feeding

Design outcomes

Primary

MeasureTime frameDescription
overall survival24 monthsDetermination for each of the 3 molecular subtypes of glioblastoma the predictive performance on 1-year overall survival of in situ immune parameters

Countries

France, Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026