Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies

In cancer chemotherapy neutropenia is a common dose-limiting toxicity. An ability to predict the neutropenic effects of cytotoxic agents based on proposed trial designs and models conditioned on previous studies would be valuable. The aim of this study was to evaluate the ability of a semi-mechanist...

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Main Authors: Soto, Elena, Keizer, Ron J., Trocóniz, Iñaki F., Huitema, Alwin D. R., Beijnen, Jos H., Schellens, Jan H. M., Wanders, Jantien, Cendrós, Josep María, Obach, Rosendo, Peraire, Concepción, Friberg, Lena E., Karlsson, Mats O.
Format: Online
Language:English
Published: Springer US 2010
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160557/
id pubmed-3160557
recordtype oai_dc
spelling pubmed-31605572011-09-26 Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies Soto, Elena Keizer, Ron J. Trocóniz, Iñaki F. Huitema, Alwin D. R. Beijnen, Jos H. Schellens, Jan H. M. Wanders, Jantien Cendrós, Josep María Obach, Rosendo Peraire, Concepción Friberg, Lena E. Karlsson, Mats O. Phase I Studies In cancer chemotherapy neutropenia is a common dose-limiting toxicity. An ability to predict the neutropenic effects of cytotoxic agents based on proposed trial designs and models conditioned on previous studies would be valuable. The aim of this study was to evaluate the ability of a semi-mechanistic pharmacokinetic/pharmacodynamic (PK/PD) model for myelosuppression to predict the neutropenia observed in Phase I clinical studies, based on parameter estimates obtained from prior trials. Pharmacokinetic and neutropenia data from 5 clinical trials for diflomotecan and from 4 clinical trials for indisulam were used. Data were analyzed and simulations were performed using the population approach with NONMEM VI. Parameter sets were estimated under the following scenarios: (a) data from each trial independently, (b) pooled data from all clinical trials and (c) pooled data from trials performed before the tested trial. Model performance in each of the scenarios was evaluated by means of predictive (visual and numerical) checks. The semi-mechanistic PK/PD model for neutropenia showed adequate predictive ability for both anti-cancer agents. For diflomotecan, similar predictions were obtained for the three scenarios. For indisulam predictions were better when based on data from the specific study, however when the model parameters were conditioned on data from trials performed prior to a specific study, similar predictions of the drug related-neutropenia profiles and descriptors were obtained as when all data were used. This work provides further indication that modeling and simulation tools can be applied in the early stages of drug development to optimize future trials. Springer US 2010-05-07 2011-10 /pmc/articles/PMC3160557/ /pubmed/20449627 http://dx.doi.org/10.1007/s10637-010-9437-z Text en © The Author(s) 2010
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Soto, Elena
Keizer, Ron J.
Trocóniz, Iñaki F.
Huitema, Alwin D. R.
Beijnen, Jos H.
Schellens, Jan H. M.
Wanders, Jantien
Cendrós, Josep María
Obach, Rosendo
Peraire, Concepción
Friberg, Lena E.
Karlsson, Mats O.
spellingShingle Soto, Elena
Keizer, Ron J.
Trocóniz, Iñaki F.
Huitema, Alwin D. R.
Beijnen, Jos H.
Schellens, Jan H. M.
Wanders, Jantien
Cendrós, Josep María
Obach, Rosendo
Peraire, Concepción
Friberg, Lena E.
Karlsson, Mats O.
Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies
author_facet Soto, Elena
Keizer, Ron J.
Trocóniz, Iñaki F.
Huitema, Alwin D. R.
Beijnen, Jos H.
Schellens, Jan H. M.
Wanders, Jantien
Cendrós, Josep María
Obach, Rosendo
Peraire, Concepción
Friberg, Lena E.
Karlsson, Mats O.
author_sort Soto, Elena
title Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies
title_short Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies
title_full Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies
title_fullStr Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies
title_full_unstemmed Predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies
title_sort predictive ability of a semi-mechanistic model for neutropenia in the development of novel anti-cancer agents: two case studies
description In cancer chemotherapy neutropenia is a common dose-limiting toxicity. An ability to predict the neutropenic effects of cytotoxic agents based on proposed trial designs and models conditioned on previous studies would be valuable. The aim of this study was to evaluate the ability of a semi-mechanistic pharmacokinetic/pharmacodynamic (PK/PD) model for myelosuppression to predict the neutropenia observed in Phase I clinical studies, based on parameter estimates obtained from prior trials. Pharmacokinetic and neutropenia data from 5 clinical trials for diflomotecan and from 4 clinical trials for indisulam were used. Data were analyzed and simulations were performed using the population approach with NONMEM VI. Parameter sets were estimated under the following scenarios: (a) data from each trial independently, (b) pooled data from all clinical trials and (c) pooled data from trials performed before the tested trial. Model performance in each of the scenarios was evaluated by means of predictive (visual and numerical) checks. The semi-mechanistic PK/PD model for neutropenia showed adequate predictive ability for both anti-cancer agents. For diflomotecan, similar predictions were obtained for the three scenarios. For indisulam predictions were better when based on data from the specific study, however when the model parameters were conditioned on data from trials performed prior to a specific study, similar predictions of the drug related-neutropenia profiles and descriptors were obtained as when all data were used. This work provides further indication that modeling and simulation tools can be applied in the early stages of drug development to optimize future trials.
publisher Springer US
publishDate 2010
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160557/
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