<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(11)</volume><submitter>Cazaubon Y</submitter><pubmed_abstract>Mitotane is the most effective agent in post-operative treatment of adrenocortical carcinoma. In adults, the starting dose is 2-3 g/day and should be slightly increased to reach the therapeutic index of 14-20 mg/L. This study developed a population PK model for mitotane and to simulate recommended/high dosing regimens. We retrospectively analyzed the data files of 38 patients with 503 plasma concentrations for the pharmacokinetic analysis. Monolix version 2019R1 was used for non-linear mixed-effects modelling. Monte Carlo simulations were performed to evaluate the probability of target attainment (PTA ≥ 14 mg/L) at one month and at three months. Mitotane concentration data were best described by a linear one-compartment model. The estimated PK parameters (between-subject variability) were:</pubmed_abstract><journal>Pharmaceutics</journal><pagination>E566</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6920765</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Population Pharmacokinetics Modelling and Simulation of Mitotane in Patients with Adrenocortical Carcinoma: An Individualized Dose Regimen to Target All Patients at Three Months?</pubmed_title><pmcid>PMC6920765</pmcid><pubmed_authors>Konecki C</pubmed_authors><pubmed_authors>Cazaubon Y</pubmed_authors><pubmed_authors>Talineau Y</pubmed_authors><pubmed_authors>Djerada Z</pubmed_authors><pubmed_authors>Russello J</pubmed_authors><pubmed_authors>Mathieu O</pubmed_authors><pubmed_authors>Feliu C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Population Pharmacokinetics Modelling and Simulation of Mitotane in Patients with Adrenocortical Carcinoma: An Individualized Dose Regimen to Target All Patients at Three Months?</name><description>Mitotane is the most effective agent in post-operative treatment of adrenocortical carcinoma. In adults, the starting dose is 2-3 g/day and should be slightly increased to reach the therapeutic index of 14-20 mg/L. This study developed a population PK model for mitotane and to simulate recommended/high dosing regimens. We retrospectively analyzed the data files of 38 patients with 503 plasma concentrations for the pharmacokinetic analysis. Monolix version 2019R1 was used for non-linear mixed-effects modelling. Monte Carlo simulations were performed to evaluate the probability of target attainment (PTA ≥ 14 mg/L) at one month and at three months. Mitotane concentration data were best described by a linear one-compartment model. The estimated PK parameters (between-subject variability) were:</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2026-05-04T08:14:00.966Z</modification><creation>2020-05-22T00:42:04Z</creation></dates><accession>S-EPMC6920765</accession><cross_references><pubmed>31683663</pubmed><doi>10.3390/pharmaceutics11110566</doi></cross_references></HashMap>