| Literature DB >> 28182273 |
C Liu1, J Yu1, H Li1, J Liu1, Y Xu1, P Song1, Q Liu1, H Zhao1, J Xu1, V E Maher1, B P Booth1, G Kim1, A Rahman1, Y Wang1.
Abstract
Nivolumab is a human monoclonal antibody that blocks the interaction between PD-1 programmed death-1 (PD-1) and its ligands, PD-L1 and PD-L2. Nivolumab demonstrated efficacy in clinical trials for various types of cancer. A time-varying clearance was identified for nivolumab. We show that the change of clearance over time is associated with the post-treatment effects: clearance decreases when disease status improves. This interaction between posttreatment effects and drug exposure may lead to a biased steep estimate of the exposure-response (E-R) relationship for efficacy. Under this scenario, simulations were performed to develop a proposed methodology to assess the causal effect of drug exposure upon clinical response. Data from nivolumab trials were subsequently used to verify the proposed methodology for E-R analysis. The results showed that E-R analysis results based on pharmacokinetic (PK) metrics derived from the first dose are more consistent with the true E-R or dose-response relationship than the steady-state PK metrics. Published 2017. This article is a U.S. Government work and is in the public domain in the USA.Entities:
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Year: 2017 PMID: 28182273 DOI: 10.1002/cpt.656
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875