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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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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 |
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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 |
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