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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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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