Clinical Pharmacokinetics and Pharmacodynamics of Immune Checkpoint Inhibitors

Immune checkpoint inhibitors (ICIs) have demonstrated signifcant clinical impact in improving overall survival of several malignancies associated with poor outcomes; however, only 20–40% of patients will show long-lasting survival. Further clarifcation of factors related to treatment response can su...

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Detalles Bibliográficos
Autores: Centanni, M. (Maddalena)|||/items/09a9d68e-0002-4991-bb99-0d7684645467, Moes, D.J.A.R. (Dirk Jan A. R.)|||/items/f540cc8d-8372-4216-8ab1-8b9afdad1ecd, Troconiz, I.F. (Iñaki F.)|||/items/e6782d1e-7a2a-42cc-95d6-55223215bf44, Ciccolini, J. (Joseph)|||/items/fd12a9f6-96e3-4574-a8c3-60da4aa15d2f, Coen-van-Hasselt, J.G. (J. G.)|||/items/0d68d8ef-19a4-464b-81f7-5f58db2096dc
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/62591
Acceso en línea:https://hdl.handle.net/10171/62591
Access Level:acceso abierto
Palabra clave:Pharmacokinetics (PK)
iImmune checkpoint inhibitors (ICIs)
Pharmacodynamics (PD)
Descripción
Sumario:Immune checkpoint inhibitors (ICIs) have demonstrated signifcant clinical impact in improving overall survival of several malignancies associated with poor outcomes; however, only 20–40% of patients will show long-lasting survival. Further clarifcation of factors related to treatment response can support improvements in clinical outcome and guide the development of novel immune checkpoint therapies. In this article, we have provided an overview of the pharmacokinetic (PK) aspects related to current ICIs, which include target-mediated drug disposition and time-varying drug clearance. In response to the variation in treatment exposure of ICIs and the signifcant healthcare costs associated with these agents, arguments for both dose individualization and generalization are provided. We address important issues related to the efcacy and safety, the pharmacodynamics (PD), of ICIs, including exposure–response relationships related to clinical outcome. The unique PK and PD aspects of ICIs give rise to issues of confounding and suboptimal surrogate endpoints that complicate interpretation of exposure–response analysis. Biomarkers to identify patients benefting from treatment with ICIs have been brought forward. However, validated biomarkers to monitor treatment response are currently lacking.