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A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients
To assess circulating biomarkers as predictors of antitumor response to atezolizumab (anti‐programmed death‐ligand 1 (PD‐L1), Tecentriq) serum pharmacokinetic (PK) and 95 plasma biomarkers were analyzed in 88 patients with relapsed/refractory non‐small cell lung cancer (NSCLC) receiving atezolizumab...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704358/ https://www.ncbi.nlm.nih.gov/pubmed/30058723 http://dx.doi.org/10.1002/cpt.1198 |
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author | Netterberg, Ida Li, Chi‐Chung Molinero, Luciana Budha, Nageshwar Sukumaran, Siddharth Stroh, Mark Jonsson, E. Niclas Friberg, Lena E. |
author_facet | Netterberg, Ida Li, Chi‐Chung Molinero, Luciana Budha, Nageshwar Sukumaran, Siddharth Stroh, Mark Jonsson, E. Niclas Friberg, Lena E. |
author_sort | Netterberg, Ida |
collection | PubMed |
description | To assess circulating biomarkers as predictors of antitumor response to atezolizumab (anti‐programmed death‐ligand 1 (PD‐L1), Tecentriq) serum pharmacokinetic (PK) and 95 plasma biomarkers were analyzed in 88 patients with relapsed/refractory non‐small cell lung cancer (NSCLC) receiving atezolizumab i.v. q3w (10–20 mg/kg) in the PCD4989g phase I clinical trial. Following exploratory analyses, two plasma biomarkers were chosen for further study and correlation with change in tumor size (the sum of the longest diameter) was assessed in a pharmacokinetic/pharmacodynamic (PK/PD) tumor modeling framework. When longitudinal kinetics of biomarkers and tumor size were modeled, tumor shrinkage was found to significantly correlate with area under the curve (AUC), baseline factors (metastatic sites, liver metastases, and smoking status), and relative change in interleukin (IL)‐18 level from baseline at day 21 (RCFB(IL) (‐18,d21)). Although AUC was a major predictor of tumor shrinkage, the effect was estimated to dissipate with an average half‐life of 80 days, whereas RCFB(IL) (‐18,d21) seemed relevant to the duration of the response. |
format | Online Article Text |
id | pubmed-6704358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67043582019-08-26 A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients Netterberg, Ida Li, Chi‐Chung Molinero, Luciana Budha, Nageshwar Sukumaran, Siddharth Stroh, Mark Jonsson, E. Niclas Friberg, Lena E. Clin Pharmacol Ther Research To assess circulating biomarkers as predictors of antitumor response to atezolizumab (anti‐programmed death‐ligand 1 (PD‐L1), Tecentriq) serum pharmacokinetic (PK) and 95 plasma biomarkers were analyzed in 88 patients with relapsed/refractory non‐small cell lung cancer (NSCLC) receiving atezolizumab i.v. q3w (10–20 mg/kg) in the PCD4989g phase I clinical trial. Following exploratory analyses, two plasma biomarkers were chosen for further study and correlation with change in tumor size (the sum of the longest diameter) was assessed in a pharmacokinetic/pharmacodynamic (PK/PD) tumor modeling framework. When longitudinal kinetics of biomarkers and tumor size were modeled, tumor shrinkage was found to significantly correlate with area under the curve (AUC), baseline factors (metastatic sites, liver metastases, and smoking status), and relative change in interleukin (IL)‐18 level from baseline at day 21 (RCFB(IL) (‐18,d21)). Although AUC was a major predictor of tumor shrinkage, the effect was estimated to dissipate with an average half‐life of 80 days, whereas RCFB(IL) (‐18,d21) seemed relevant to the duration of the response. John Wiley and Sons Inc. 2018-09-04 2019-02 /pmc/articles/PMC6704358/ /pubmed/30058723 http://dx.doi.org/10.1002/cpt.1198 Text en © 2018 The Authors Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of 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 Netterberg, Ida Li, Chi‐Chung Molinero, Luciana Budha, Nageshwar Sukumaran, Siddharth Stroh, Mark Jonsson, E. Niclas Friberg, Lena E. A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients |
title | A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients |
title_full | A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients |
title_fullStr | A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients |
title_full_unstemmed | A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients |
title_short | A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients |
title_sort | pk/pd analysis of circulating biomarkers and their relationship to tumor response in atezolizumab‐treated non‐small cell lung cancer patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6704358/ https://www.ncbi.nlm.nih.gov/pubmed/30058723 http://dx.doi.org/10.1002/cpt.1198 |
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