izpis_h1_title_alt

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

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Izvleček
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.

Jezik:Angleški jezik
Ključne besede:ustekinumab, inflammatory bowel disease, fecal calprotectin, pharmacokinetics-pharmacodynamics, therapeutic drug monitoring
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FFA - Fakulteta za farmacijo
MF - Medicinska fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2021
Št. strani:16 str.
Številčenje:Vol. 13, iss. 10, art. 1587
PID:20.500.12556/RUL-136291 Povezava se odpre v novem oknu
UDK:615.277.3:616.344-002
ISSN pri članku:1999-4923
DOI:10.3390/pharmaceutics13101587 Povezava se odpre v novem oknu
COBISS.SI-ID:78625027 Povezava se odpre v novem oknu
Datum objave v RUL:22.04.2022
Število ogledov:671
Število prenosov:114
Metapodatki:XML RDF-CHPDL DC-XML DC-RDF
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Gradivo je del revije

Naslov:Pharmaceutics
Skrajšan naslov:Pharmaceutics
Založnik:MDPI
ISSN:1999-4923
COBISS.SI-ID:517949977 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:01.10.2021

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:vnetje črevesja, terapevtsko spremljanje zdravil, fekalni kalprotektin, Crohnova bolezen, tarčna zdravila

Projekti

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P1-0189
Naslov:Farmacevtska tehnologija: od dostavnih sistemov učinkovin do terapijskih izidov zdravil pri otrocih in starostnikih

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