This phase I trial evaluates whether a short course of disulfiram before surgery improves immune system response in patients with high-grade glioma. High-grade gliomas create a tumor environment that suppresses the body’s immune system. Special immune cells inside the tumor, called myeloid cells, can become immunosuppressive, meaning they prevent the body’s own immune system from recognizing and attacking the tumor effectively. This immune suppression is one of the major reasons immunotherapies, a type of cancer therapy that has shown promise in many other cancer types, have not worked well in glioblastoma. In laboratory studies, disulfiram reduces the release of inflammatory signals that drive these immunosuppressive myeloid cells. By reducing these signals, disulfiram may work to “reprogram” the tumor microenvironment so that the body’s immune system can function more effectively.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07719127.
Locations matching your search criteria
United States
Ohio
Cleveland
Case Comprehensive Cancer CenterStatus: Approved
Contact: Tiffany Hodges
Phone: 216-286-7122
PRIMARY OBJECTIVE:
I. Evaluate whether pre-operative disulfiram reduces the complement immunosuppressive and the scavenger immunosuppressive myeloid program in resected tumor tissue.
SECONDARY OBJECTIVES:
I. Evaluate whether disulfiram reduces vasogenic edema-related symptoms and reduces/delays the need for dexamethasone during the pre-operative window.
II. Assess the change in microglial inflammatory and systemic inflammatory program usage by myeloid cells in the tumor microenvironment.
III. Characterize the safety and tolerability of disulfiram in the peri-operative and pre-operative setting.
EXPLORATORY OBJECTIVES:
I. Assess changes in T cell phenotypes (activation/exhaustion) and other immune and tumor cell states as proxies of immunosuppression.
II. Explore associations between cytokine changes(e.g. IL-1beta, tumor necrosis factor [TNF], IL-12, IL-6, IL-8, and interferon gamma [IFNG]), myeloid programs, spatial niches, and clinical symptom response.
CORRELATIVE OBJECTIVES:
I. Quantify plasma IL-1beta and inflammatory cytokine changes (Luminex) from baseline to pre-operative timepoint.
II. Quantify tumor IL-1beta biology (ribonucleic acid [RNA] and/or protein where feasible) and pyroptosis signature activity.
III. Quantify scavenger and complement myeloid program scores and compare to institutional historical controls using single-cell RNA sequencing.
IV. Map spatial localization of IL-1beta biology, myeloid programs, and immune interactions using spatial transcriptomics.
OUTLINE: This is a phase I dose-escalation study of disulfiram.
Patients receive disulfiram orally (PO) once daily (QD) for 3-14 days, up to the day prior to standard of care surgery. Patients also undergo collection of blood, tissue, and cerebrospinal fluid (CSF) samples on study.
After completion of study treatment, patients are followed up for 14 days post-operatively.
Lead OrganizationCase Comprehensive Cancer Center
Principal InvestigatorTiffany Hodges