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Phase I dose-escalation, safety, and CNS pharmacokinetic study of dexanabinol in patients with brain cancer.
- Source :
-
Neuro-oncology advances [Neurooncol Adv] 2021 Feb 15; Vol. 3 (1), pp. vdab006. Date of Electronic Publication: 2021 Feb 15 (Print Publication: 2021). - Publication Year :
- 2021
-
Abstract
- Background: Dexanabinol is a synthetic analogue of tetrahydrocannabinol identified as a potential anti-cancer therapeutic by e-Therapeutics PLC. Dexanabinol was selected for further investigation based on its preclinical tumoricidal activity. This phase I dose-escalation trial examined the safety, drug penetration into the central nervous system (CNS), preliminary antitumor activity, and recommended phase II dose.<br />Methods: Dexanabinol formulated in cremophor/ethanol was administered once weekly via 3-hour intravenous infusion to patients with brain cancer.<br />Results: A total of 26 patients were dosed once weekly at 2, 4, 8, 16, 24, 28, and 36 mg/kg. Two patients at 36 mg/kg were nonevaluable for dose level confirmation, having withdrawn early for reasons unrelated to study treatment. A recommended phase II dose of dexanabinol was established at 28 mg/kg due to related, reversible adverse events at higher dose levels that required medications for symptomatic relief. The most common drug-related toxicities were the depressed level of consciousness and lightheadedness, diarrhea, itching, fatigue, chest discomfort, and tingling in the mouth. Systemic exposure to dexanabinol (AUC <subscript>0- t </subscript> and C <subscript>max</subscript> ) increased from 2 to 36 mg/kg, with dose nonproportionality apparent at the highest dose; dexanabinol was present in appreciable levels in the cerebrospinal fluid (CSF), which implies the possibility of exposure of intracranial tumors to drug. Five of 24 efficacy-evaluable patients (21%) experienced stable disease with a median duration of 2 cycles (28-day cycle) as the best response.<br />Conclusions: Dexanabinol administered weekly by intravenous infusion was safe and well-tolerated up to 28 mg/kg in brain cancer patients, but has limited antitumor activity in patients with brain cancer.<br /> (© The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.)
Details
- Language :
- English
- ISSN :
- 2632-2498
- Volume :
- 3
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Neuro-oncology advances
- Publication Type :
- Academic Journal
- Accession number :
- 33615223
- Full Text :
- https://doi.org/10.1093/noajnl/vdab006