4.6 Article

Neuropharmacological Study of Posaconazole for Glioblastoma: A Phase 0 Clinical Trial Protocol

Journal

NEUROSURGERY
Volume 91, Issue 4, Pages 658-665

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1227/neu.0000000000002071

Keywords

Glioblastoma; High-grade glioma; Posaconazole; Azoles; Clinical trial; Phase 0; Protocol; Drug repurposing; Microdialysis; Neuropharmacokinetics; Pharmacodynamics; Cancer metabolism; Safety

Funding

  1. National Cancer Institute of the National Institutes of Health [1R03CA255992]
  2. American Cancer Society Institutional Research Grant [IRG-17-175-04]

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This study aims to evaluate the therapeutic effects of repurposed posaconazole (PCZ) in patients with glioblastoma (GBM). The study will analyze the tumor penetrance, neuropharmacokinetics, and the impact of PCZ on tumor cell metabolism. Successful trial results will contribute to finding more effective treatment options for GBM.
BACKGROUND: Glioblastoma (GBM) is the most common malignant primary brain tumor with a universally poor prognosis. GBMs express elevated levels of hexokinase 2 (HK2), catalyzing the critical step in glycolysis and influencing several oncogenic pathways. Previous preclinical work has suggested a role for repurposed posaconazole (PCZ) in downregulating HK2 activity, reducing lactate and pyruvate production, interfering with tumor cell metabolism, and increasing mouse survival. OBJECTIVE: To establish brain tumor penetrance, neuropharmacokinetic profile, and mechanistic effect on tumor cell metabolism of PCZ in adults with GBM. METHODS: This is an open label, nonrandomized, parallel arm trial involving patients with GBM. Cohorts will receive PCZ (intervention, n = 5) or will not receive PCZ (control, n = 5), followed by tumor resection and microdialysis catheter placement. Dialysate, plasma, and tumor samples will be analyzed for lactate and pyruvate concentrations. Tumor samples will also be assessed for PCZ concentration, HK2 expression, angiogenesis, and apoptosis. PCZ's neuropharmacokinetics will be determined based on the concentration vs time profile and area under the curve 0 to 24 hours of PCZ concentration in the brain interstitium. EXPECTED OUTCOMES: (1) Increased PCZ concentration in contrast-enhancing brain regions compared with nonenhancing regions; (2) inverse correlation between lactate/pyruvate and PCZ concentrations in dialysate samples from treated patients, over time; and (3) decreased HK2 activity in PCZ-treated tumor samples. DISCUSSION: A successful trial will support the decision to proceed to advanced phase trials. Any tumor penetration by PCZ, with concomitant effect on glycolysis, warrants further in-depth analysis, as therapeutic options for these deadly tumors are currently limited.

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