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...

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Main Authors: Kinjal Sanghavi, Jason Zhang, Xiaochen Zhao, Yan Feng, Paul Statkevich, Jennifer Sheng, Amit Roy, Heather E. Vezina
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:CPT: Pharmacometrics & Systems Pharmacology
Online Access:https://doi.org/10.1002/psp4.12477
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spelling doaj-8b5d6cdfd9e449599886ab4619a8b1d32020-11-25T03:08:09ZengWileyCPT: Pharmacometrics & Systems Pharmacology2163-83062020-01-0191293910.1002/psp4.12477Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid TumorsKinjal Sanghavi0Jason Zhang1Xiaochen Zhao2Yan Feng3Paul Statkevich4Jennifer Sheng5Amit Roy6Heather E. Vezina7Bristol‐Myers Squibb Princeton New Jersey USABristol‐Myers Squibb Princeton New Jersey USABristol‐Myers Squibb Princeton New Jersey USABristol‐Myers Squibb Princeton New Jersey USABristol‐Myers Squibb Princeton New Jersey USABristol‐Myers Squibb Princeton New Jersey USABristol‐Myers Squibb Princeton New Jersey USABristol‐Myers Squibb Princeton New Jersey USAIpilimumab 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.https://doi.org/10.1002/psp4.12477
collection DOAJ
language English
format Article
sources DOAJ
author Kinjal Sanghavi
Jason Zhang
Xiaochen Zhao
Yan Feng
Paul Statkevich
Jennifer Sheng
Amit Roy
Heather E. Vezina
spellingShingle Kinjal Sanghavi
Jason Zhang
Xiaochen Zhao
Yan Feng
Paul Statkevich
Jennifer Sheng
Amit Roy
Heather E. Vezina
Population Pharmacokinetics of Ipilimumab in Combination With Nivolumab in Patients With Advanced Solid Tumors
CPT: Pharmacometrics & Systems Pharmacology
author_facet Kinjal Sanghavi
Jason Zhang
Xiaochen Zhao
Yan Feng
Paul Statkevich
Jennifer Sheng
Amit Roy
Heather E. Vezina
author_sort Kinjal Sanghavi
title 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_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_sort population pharmacokinetics of ipilimumab in combination with nivolumab in patients with advanced solid tumors
publisher Wiley
series CPT: Pharmacometrics & Systems Pharmacology
issn 2163-8306
publishDate 2020-01-01
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.
url https://doi.org/10.1002/psp4.12477
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