Cargando…

Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors

Ipilimumab is a fully human monoclonal antibody approved for the treatment of melanoma as monotherapy and for the treatment of melanoma, renal cell carcinoma, and colorectal cancer in combination with nivolumab. Ipilimumab time‐varying clearance (CL) was assessed by a population pharmacokinetics (PP...

Descripción completa

Detalles Bibliográficos
Autores principales: Sanghavi, Kinjal, Zhang, Jason, Zhao, Xiaochen, Feng, Yan, Statkevich, Paul, Sheng, Jennifer, Roy, Amit, Vezina, Heather E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966186/
https://www.ncbi.nlm.nih.gov/pubmed/31709718
http://dx.doi.org/10.1002/psp4.12477
_version_ 1783488696664719360
author Sanghavi, Kinjal
Zhang, Jason
Zhao, Xiaochen
Feng, Yan
Statkevich, Paul
Sheng, Jennifer
Roy, Amit
Vezina, Heather E.
author_facet Sanghavi, Kinjal
Zhang, Jason
Zhao, Xiaochen
Feng, Yan
Statkevich, Paul
Sheng, Jennifer
Roy, Amit
Vezina, Heather E.
author_sort Sanghavi, Kinjal
collection PubMed
description Ipilimumab is a fully human monoclonal antibody approved for the treatment of melanoma as monotherapy and for the treatment of melanoma, renal cell carcinoma, and colorectal cancer in combination with nivolumab. Ipilimumab time‐varying clearance (CL) was assessed by a population pharmacokinetics (PPK) model developed using statistically significant covariates identified in a previous PPK analysis plus additional covariates. Data from 3,411 patients who received ipilimumab 0.3–10 mg/kg alone or in combination with nivolumab in 16 clinical trials were analyzed. Ipilimumab CL decreased over time; the change in CL was greater in patients treated with nivolumab combination than ipilimumab alone and in responders vs. nonresponders. Time‐varying covariates including body weight, lactate dehydrogenase, albumin, and performance status were evaluated on change in ipilimumab CL. In addition, ipilimumab CL was similar across different tumor types, nivolumab dosing regimens, and lines of therapy. These data suggest an association of ipilimumab CL with disease severity.
format Online
Article
Text
id pubmed-6966186
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-69661862020-01-27 Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors Sanghavi, Kinjal Zhang, Jason Zhao, Xiaochen Feng, Yan Statkevich, Paul Sheng, Jennifer Roy, Amit Vezina, Heather E. CPT Pharmacometrics Syst Pharmacol Research Ipilimumab is a fully human monoclonal antibody approved for the treatment of melanoma as monotherapy and for the treatment of melanoma, renal cell carcinoma, and colorectal cancer in combination with nivolumab. Ipilimumab time‐varying clearance (CL) was assessed by a population pharmacokinetics (PPK) model developed using statistically significant covariates identified in a previous PPK analysis plus additional covariates. Data from 3,411 patients who received ipilimumab 0.3–10 mg/kg alone or in combination with nivolumab in 16 clinical trials were analyzed. Ipilimumab CL decreased over time; the change in CL was greater in patients treated with nivolumab combination than ipilimumab alone and in responders vs. nonresponders. Time‐varying covariates including body weight, lactate dehydrogenase, albumin, and performance status were evaluated on change in ipilimumab CL. In addition, ipilimumab CL was similar across different tumor types, nivolumab dosing regimens, and lines of therapy. These data suggest an association of ipilimumab CL with disease severity. John Wiley and Sons Inc. 2019-12-01 2020-01 /pmc/articles/PMC6966186/ /pubmed/31709718 http://dx.doi.org/10.1002/psp4.12477 Text en © 2019 Bristol‐Myers Squibb. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals, Inc. on behalf of the American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
Sanghavi, Kinjal
Zhang, Jason
Zhao, Xiaochen
Feng, Yan
Statkevich, Paul
Sheng, Jennifer
Roy, Amit
Vezina, Heather E.
Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors
title Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors
title_full Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors
title_fullStr Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors
title_full_unstemmed Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors
title_short Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors
title_sort population pharmacokinetics of ipilimumab in combination with nivolumab in patients with advanced solid tumors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966186/
https://www.ncbi.nlm.nih.gov/pubmed/31709718
http://dx.doi.org/10.1002/psp4.12477
work_keys_str_mv AT sanghavikinjal populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors
AT zhangjason populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors
AT zhaoxiaochen populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors
AT fengyan populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors
AT statkevichpaul populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors
AT shengjennifer populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors
AT royamit populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors
AT vezinaheathere populationpharmacokineticsofipilimumabincombinationwithnivolumabinpatientswithadvancedsolidtumors