izpis_h1_title_alt

Ustekinumab dosing individualization in Crohn's disease guided by a population pharmacokinetic-pharmacodynamic model
ID Zdovc, Jurij (Author), ID Hanžel, Jurij (Author), ID Štabuc, Borut (Author), ID Vovk, Tomaž (Author), ID Ostanek, Barbara (Author), ID Drobne, David (Author), ID Grabnar, Iztok (Author), et al.

.pdfPDF - Presentation file, Download (1,20 MB)
MD5: E539DCA5F8E73B04072A452578D49659
URLURL - Source URL, Visit https://www.mdpi.com/1999-4923/13/10/1587 This link opens in a new window

Abstract
Ustekinumab is a monoclonal antibody used in Crohn’s disease (CD). Dose optimization in case of non-response and the role of pharmacokinetic–pharmacodynamic (PK-PD) monitoring remain unresolved dilemmas in clinical practice. We aimed to develop a population PK-PD model for ustekinumab in CD and simulate efficacy of alternative dosing regimens. We included 57 patients and recorded their characteristics during 32 weeks after starting with ustekinumab therapy. Serum ustekinumab concentration was prospectively measured and fecal calprotectin (FC) concentration was used to monitor the disease activity. Ustekinumab PK-PD was described by a two-compartment target-mediated drug disposition model linked to an indirect response model. Lower fat-free mass, higher serum albumin, previous non-exposure to biologics, FCGR3A-158 V/V variant and lower C-reactive protein were associated with higher ustekinumab exposure. Model-based simulation suggested that 41.9% of patients receiving standard dosing achieve biochemical remission at week 32. In patients not achieving remission with standard dosing at week 16, transition to 4-weekly subcutaneous maintenance dosing with or without intravenous reinduction resulted in comparably higher remission rates at week 32 (51.1% vs. 49.2%, respectively). Our findings could be used to guide stratified ustekinumab treatment in CD, particularly in patients with unfavorable characteristics, who might benefit from early transition to 4-weekly maintenance dosing.

Language:English
Keywords:ustekinumab, inflammatory bowel disease, fecal calprotectin, pharmacokinetics-pharmacodynamics, therapeutic drug monitoring
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FFA - Faculty of Pharmacy
MF - Faculty of Medicine
Publication status:Published
Publication version:Version of Record
Year:2021
Number of pages:16 str.
Numbering:Vol. 13, iss. 10, art. 1587
PID:20.500.12556/RUL-136291 This link opens in a new window
UDC:615.277.3:616.344-002
ISSN on article:1999-4923
DOI:10.3390/pharmaceutics13101587 This link opens in a new window
COBISS.SI-ID:78625027 This link opens in a new window
Publication date in RUL:22.04.2022
Views:647
Downloads:113
Metadata:XML RDF-CHPDL DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Record is a part of a journal

Title:Pharmaceutics
Shortened title:Pharmaceutics
Publisher:MDPI
ISSN:1999-4923
COBISS.SI-ID:517949977 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:01.10.2021

Secondary language

Language:Slovenian
Keywords:vnetje črevesja, terapevtsko spremljanje zdravil, fekalni kalprotektin, Crohnova bolezen, tarčna zdravila

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P1-0189
Name:Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back