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Glutamate Excitotoxicity and Its Role in Glioblastoma Biology

Role of Glutamate-mediate Excitotoxicity in Invasion and Progression Processes of Glioblastoma Multiforme

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05775458
Enrollment
50
Registered
2023-03-20
Start date
2020-06-01
Completion date
2029-09-30
Last updated
2025-06-11

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

Conditions

Brain Tumor, Primary

Keywords

Brain tumor, Glutamate

Brief summary

Gliomas are the most frequent type of primary brain tumors in adults; among them glioblastoma multiforme (GBM) is the most malignant, being associated with the worst prognosis. Glutamate (Glu) is an aminoacid, responsible for essential functions in the Central Nervous System (CNS), acting both as metabolite and neurotransmitter. It is essential for regulating cellular metabolism and developmental synaptogenesis, cellular migration, differentiation and death. Recent scientific evidences have demonstrated alteration in Glu synthesis and signaling being directly involved in GBM growth and invasion

Detailed description

Glu and its scavenger's levels are measurable both in serum and in the cerebral-spinal fluid (CSF), thus making them ideal markers for tumor aggressiveness and disease activity as well as a potential target for new therapeutic approaches. Serum and CSF levels of glutamic oxaloacetic transaminase (GOT1), Glutamate Pyruvate Transaminase (GPT) and glutamate and aspartate levels of a total of 40 patients will be collected. Molecular biology analyses will be conducted and oncological and imaging data will be collected during follow-up in patients enrolled in the present studies. MRI imaging as well as blood sampling will be performed at definite timepoints (baseline and 3, 6 and 9 months follow-up).

Interventions

DIAGNOSTIC_TESTBlood, CSF and tumor samples

Blood, CSF and brain tissue sampling of Glu and Glu regulatory proteins.

Sponsors

IRCCS San Raffaele
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Adult patients with a brain lesion suspected for GBM, candidate to gross total tumor resection (GTR), followed by radiotherapy and chemotherapy (concomitant and adjuvant). * Patient able to provide informed consent.

Exclusion criteria

* Age \< 18 years * Liver disease * Severe anemia (Hb \<8mg/dl) * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Baseline characterization of Glutamate scavengers (Glu-sca) levels in serumBaseline (before surgery)Serum GOT1 (UI/ml), GPT (UI/ml)
Baseline characterization of Glutamate (Glu) levels in serumBaseline (before surgery)Serum Glutamate (μM/L)
Time changes in Glutamate scavengers (Glu-sca) levels in serumAt 3, 6, 9 months following surgerySerum GOT1 (UI/ml), GPT (UI/ml)
Time changes in Glutamate (Glu) levels in serumAt 3, 6, 9 months following surgerySerum Glutamate (μM/L)

Secondary

MeasureTime frameDescription
Characterization of Glutamate scavengers (Glu-sca) levels in cerebrospinal fluid (CSF)Baseline (before surgery)CSF levels GOT1 (UI/ml), GPT (UI/ml)
Characterization of Glutamate (Glu) levels in cerebrospinal fluid (CSF)Baseline (before surgery)CSF levels Glutamate (μM/L)

Other

MeasureTime frameDescription
Association between Glutamate metabolism and Glioblastoma molecular signatureBaseline levels of markersAssociation between Glu and Glu-scavengers' levels and molecular patterns of Glioblastoma as described by 2021 WHO classification

Countries

Italy

Contacts

Primary ContactSincinelli Laura
sincinelli.laura@hsr.it0226436658

Outcome results

None listed

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