A phase 0 analysis of ixazomib in patients with glioblastoma.

Autor: Quillin J; Department of Neurosurgery, Emory University, Atlanta, GA 30322, USA., Patel R; Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA., Herzberg E; Covance Laboratories, Inc., Madison, WI 53704, USA., Alton D; Covance Laboratories, Inc., Madison, WI 53704, USA., Bikzhanova G; Covance Laboratories, Inc., Madison, WI 53704, USA., Geisler L; Covance Laboratories, Inc., Madison, WI 53704, USA., Olson J; Department of Neurosurgery, Emory University, Atlanta, GA 30322, USA.
Jazyk: angličtina
Zdroj: Molecular and clinical oncology [Mol Clin Oncol] 2020 Nov; Vol. 13 (5), pp. 43. Date of Electronic Publication: 2020 Aug 13.
DOI: 10.3892/mco.2020.2114
Abstrakt: Improving overall survival in recurrent glioblastoma remains a challenge, and drugs acting by unique mechanisms are urgently required. Ixazomib is an orally-administered proteasome inhibitor used in combination with lenalidomide and dexamethasone to treat patients with multiple myeloma who have received at least one prior therapy. However, ixazomib's ability to reach brain tumors has not been studied during its development. The aim of the present study (ClinicalTrials.gov, NCT02630030) was to establish and quantify ixazomib's presence in glioblastoma. The present study investigated 3 patients with recurrent glioblastoma after administration of oral ixazomib citrate (MLN 9708) at a fixed 4.0 mg dose within a 3-hpreoperative window. A total of 2 blood samples were taken from each patient at the time of incision, tumor sampling and closure. Brain tumor samples were collected during tumor resection. These samples were then used to measure the plasma and brain tumor tissue concentration of the biologically-active form of ixazomib (MLN 2238). Patient 1 had plasma concentrations of ixazomib averaging 26.2, 21.8 and 15.3 ng/ml at incision, tumor sampling and closure, respectively. The brain tumor tissue concentration was 7.88 ng/g. Patient 2 had the same interval and brain tumor tissue measurements of 19.0, 18.0 and 8.93 ng/ml, and 2.03 ng/g. Patient 3 had plasma concentration interval measurements of 25.6, 36.2 and 28.7 ng/ml. Multiple brain tumor tissue samples were taken in patient 3, with an average tissue ixazomib concentration of 3.37 ng/g. Ixazomib was found at plasma concentrations commensurate with its previously established pharmacokinetic profile without clinically relevant drug-related adverse events. Ixazomib reaches glioblastoma tissues at measurable concentrations at the time of tumor resection, confirming target tissue delivery. This justifies the phase I study of ixazomib in recurrent glioblastoma currently in development.
(Copyright © 2020, Spandidos Publications.)
Databáze: MEDLINE
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