A phase Ib/II randomized, open-label drug repurposing trial of glutamate signaling inhibitors in combination with chemoradiotherapy in patients with newly diagnosed glioblastoma: the GLUGLIO trial protocol.

Détails

ID Serval
serval:BIB_5EBA66D24C63
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A phase Ib/II randomized, open-label drug repurposing trial of glutamate signaling inhibitors in combination with chemoradiotherapy in patients with newly diagnosed glioblastoma: the GLUGLIO trial protocol.
Périodique
BMC cancer
Auteur⸱e⸱s
Mastall M., Roth P., Bink A., Fischer Maranta A., Läubli H., Hottinger A.F., Hundsberger T., Migliorini D., Ochsenbein A., Seystahl K., Imbach L., Hortobagyi T., Held L., Weller M., Wirsching H.G.
ISSN
1471-2407 (Electronic)
ISSN-L
1471-2407
Statut éditorial
Publié
Date de publication
15/01/2024
Peer-reviewed
Oui
Volume
24
Numéro
1
Pages
82
Langue
anglais
Notes
Publication types: Clinical Trial Protocol ; Journal Article
Publication Status: epublish
Résumé
Glioblastoma is the most common and most aggressive malignant primary brain tumor in adults. Glioblastoma cells synthesize and secrete large quantities of the excitatory neurotransmitter glutamate, driving epilepsy, neuronal death, tumor growth and invasion. Moreover, neuronal networks interconnect with glioblastoma cell networks through glutamatergic neuroglial synapses, activation of which induces oncogenic calcium oscillations that are propagated via gap junctions between tumor cells. The primary objective of this study is to explore the efficacy of brain-penetrating anti-glutamatergic drugs to standard chemoradiotherapy in patients with glioblastoma.
GLUGLIO is a 1:1 randomized phase Ib/II, parallel-group, open-label, multicenter trial of gabapentin, sulfasalazine, memantine and chemoradiotherapy (Arm A) versus chemoradiotherapy alone (Arm B) in patients with newly diagnosed glioblastoma. Planned accrual is 120 patients. The primary endpoint is progression-free survival at 6 months. Secondary endpoints include overall and seizure-free survival, quality of life of patients and caregivers, symptom burden and cognitive functioning. Glutamate levels will be assessed longitudinally by magnetic resonance spectroscopy. Other outcomes of interest include imaging response rate, neuronal hyperexcitability determined by longitudinal electroencephalography, Karnofsky performance status as a global measure of overall performance, anticonvulsant drug use and steroid use. Tumor tissue and blood will be collected for translational research. Subgroup survival analyses by baseline parameters include segregation by age, extent of resection, Karnofsky performance status, O <sup>6</sup> -methylguanine DNA methyltransferase (MGMT) promotor methylation status, steroid intake, presence or absence of seizures, tumor volume and glutamate levels determined by MR spectroscopy. The trial is currently recruiting in seven centers in Switzerland.
NCT05664464. Registered 23 December 2022.
Mots-clé
Adult, Humans, Brain Neoplasms/drug therapy, Brain Neoplasms/genetics, Chemoradiotherapy, Clinical Trials, Phase I as Topic, Clinical Trials, Phase II as Topic, Drug Repositioning, Glioblastoma/drug therapy, Glioblastoma/genetics, Glutamates, Multicenter Studies as Topic, Quality of Life, Randomized Controlled Trials as Topic, Steroids/therapeutic use, Cancer neuroscience, Epilepsy, Gabapentin, Memantine, Sulfasalazine
Pubmed
Web of science
Open Access
Oui
Création de la notice
18/01/2024 16:28
Dernière modification de la notice
13/02/2024 8:23
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