Systems Modeling of Bortezomib and Dexamethasone Combinatorial Effects on Bone Homeostasis in Multiple Myeloma Patients.
PK/PD modeling
cancer
cancer chemotherapy
drug-drug interaction
in silico modeling
mechanistic modeling
systems pharmacology
Journal
Journal of pharmaceutical sciences
ISSN: 1520-6017
Titre abrégé: J Pharm Sci
Pays: United States
ID NLM: 2985195R
Informations de publication
Date de publication:
Jan 2019
Jan 2019
Historique:
received:
23
08
2018
revised:
03
11
2018
accepted:
07
11
2018
pubmed:
26
11
2018
medline:
20
2
2020
entrez:
26
11
2018
Statut:
ppublish
Résumé
Osteolytic bone disease is one of the most debilitating manifestations of multiple myeloma (MM). Bortezomib is a proteasome inhibitor that shows both anticancer and bone anabolic properties and is being evaluated for its positive effects in MM patients with skeletal complications. Dexamethasone is a potent corticosteroid that is often given in combination with bortezomib for its antineoplastic effects; however, bone loss and osteoporosis are major adverse effects of long-term steroid-based therapies. In this study, a small systems pharmacological model was developed to integrate the bone anabolic effects of bortezomib with the osteolytic activity of dexamethasone in MM patients with bone disease. The final model parameters were all estimated with good precision. The interaction model is based on codifying multiple regulatory mechanisms of drug action and provides a platform for probing optimized bortezomib and dexamethasone combination dosing regimens to minimize skeletal side effects during myeloma therapy.
Identifiants
pubmed: 30472266
pii: S0022-3549(18)30729-9
doi: 10.1016/j.xphs.2018.11.024
pmc: PMC6495529
mid: NIHMS1514233
pii:
doi:
Substances chimiques
Proteasome Inhibitors
0
Bortezomib
69G8BD63PP
Dexamethasone
7S5I7G3JQL
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
732-740Subventions
Organisme : NIGMS NIH HHS
ID : R01 GM057980
Pays : United States
Informations de copyright
Copyright © 2019 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.