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Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer

PURPOSE: A prospective, multicenter, large-scale cohort with a nested case–control study (NCT00252759) was conducted to identify and quantify risk factors for interstitial lung disease (ILD) in Japanese patients with non-small-cell lung cancer who received gefitinib. This study reports the associati...

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Autores principales: Kawata, Toshio, Higashimori, Mitsuo, Itoh, Yohji, Tomkinson, Helen, Johnson, Martin G., Tang, Weifeng, Nyberg, Fredrik, Jiang, Haiyi, Tanigawara, Yusuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458983/
https://www.ncbi.nlm.nih.gov/pubmed/30762084
http://dx.doi.org/10.1007/s00280-019-03788-4
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author Kawata, Toshio
Higashimori, Mitsuo
Itoh, Yohji
Tomkinson, Helen
Johnson, Martin G.
Tang, Weifeng
Nyberg, Fredrik
Jiang, Haiyi
Tanigawara, Yusuke
author_facet Kawata, Toshio
Higashimori, Mitsuo
Itoh, Yohji
Tomkinson, Helen
Johnson, Martin G.
Tang, Weifeng
Nyberg, Fredrik
Jiang, Haiyi
Tanigawara, Yusuke
author_sort Kawata, Toshio
collection PubMed
description PURPOSE: A prospective, multicenter, large-scale cohort with a nested case–control study (NCT00252759) was conducted to identify and quantify risk factors for interstitial lung disease (ILD) in Japanese patients with non-small-cell lung cancer who received gefitinib. This study reports the association between gefitinib exposure and the occurrence of ILD. METHODS: A total of 1891 gefitinib plasma concentrations from 336 patients were measured after first dose, at steady state, and at time of ILD occurrence. Influences of demographic and pathophysiological factors on pharmacokinetics were investigated by non-linear mixed-effect modeling. The exposure to gefitinib was compared between patients without and with ILD occurrence to explore risks associated with gefitinib-induced ILD. Intra-patient comparison of exposure was also conducted between times at ILD development and normal states. RESULTS: In the population pharmacokinetic analysis for gefitinib, α(1)-acid glycoprotein (AGP), age, body weight, and concomitant use of cytochrome P450 3A4 inducers were significant covariates on oral clearance (CL/F). AGP and body weight were also identified as factors affecting the volume of distribution. CL/F was significantly lower at the time of ILD occurrence than normal states. Patients who developed ILD tended to show higher exposure to gefitinib than those without ILD; however, these differences were not statistically significant. On the other hand, exposure at the time of ILD occurrence was significantly elevated compared to the time of normal state within the same patients. CONCLUSIONS: Significant elevation of exposure of gefitinib was observed at the time of ILD occurrence, suggesting reduction of CL/F could be associated with ILD-induced AGP elevation. Increase in exposure of gefitinib is unlikely to be a robust predictor of ILD and does not warrant any dose modifications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00280-019-03788-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-64589832019-05-03 Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer Kawata, Toshio Higashimori, Mitsuo Itoh, Yohji Tomkinson, Helen Johnson, Martin G. Tang, Weifeng Nyberg, Fredrik Jiang, Haiyi Tanigawara, Yusuke Cancer Chemother Pharmacol Original Article PURPOSE: A prospective, multicenter, large-scale cohort with a nested case–control study (NCT00252759) was conducted to identify and quantify risk factors for interstitial lung disease (ILD) in Japanese patients with non-small-cell lung cancer who received gefitinib. This study reports the association between gefitinib exposure and the occurrence of ILD. METHODS: A total of 1891 gefitinib plasma concentrations from 336 patients were measured after first dose, at steady state, and at time of ILD occurrence. Influences of demographic and pathophysiological factors on pharmacokinetics were investigated by non-linear mixed-effect modeling. The exposure to gefitinib was compared between patients without and with ILD occurrence to explore risks associated with gefitinib-induced ILD. Intra-patient comparison of exposure was also conducted between times at ILD development and normal states. RESULTS: In the population pharmacokinetic analysis for gefitinib, α(1)-acid glycoprotein (AGP), age, body weight, and concomitant use of cytochrome P450 3A4 inducers were significant covariates on oral clearance (CL/F). AGP and body weight were also identified as factors affecting the volume of distribution. CL/F was significantly lower at the time of ILD occurrence than normal states. Patients who developed ILD tended to show higher exposure to gefitinib than those without ILD; however, these differences were not statistically significant. On the other hand, exposure at the time of ILD occurrence was significantly elevated compared to the time of normal state within the same patients. CONCLUSIONS: Significant elevation of exposure of gefitinib was observed at the time of ILD occurrence, suggesting reduction of CL/F could be associated with ILD-induced AGP elevation. Increase in exposure of gefitinib is unlikely to be a robust predictor of ILD and does not warrant any dose modifications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00280-019-03788-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-02-14 2019 /pmc/articles/PMC6458983/ /pubmed/30762084 http://dx.doi.org/10.1007/s00280-019-03788-4 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Kawata, Toshio
Higashimori, Mitsuo
Itoh, Yohji
Tomkinson, Helen
Johnson, Martin G.
Tang, Weifeng
Nyberg, Fredrik
Jiang, Haiyi
Tanigawara, Yusuke
Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer
title Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer
title_full Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer
title_fullStr Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer
title_full_unstemmed Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer
title_short Gefitinib exposure and occurrence of interstitial lung disease in Japanese patients with non-small-cell lung cancer
title_sort gefitinib exposure and occurrence of interstitial lung disease in japanese patients with non-small-cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458983/
https://www.ncbi.nlm.nih.gov/pubmed/30762084
http://dx.doi.org/10.1007/s00280-019-03788-4
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