13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

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

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          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.

          Related collections

          Most cited references22

          • Record: found
          • Abstract: found
          • Article: found

          Prediction of Creatinine Clearance from Serum Creatinine

          A formula has been developed to predict creatinine clearance (C cr ) from serum creatinine (S cr ) in adult males: Ccr = (140 – age) (wt kg)/72 × S cr (mg/100ml) (15% less in females). Derivation included the relationship found between age and 24-hour creatinine excretion/kg in 249 patients aged 18–92. Values for C cr were predicted by this formula and four other methods and the results compared with the means of two 24-hour C cr’s measured in 236 patients. The above formula gave a correlation coefficient between predicted and mean measured Ccr·s of 0.83; on average, the difference between predicted and mean measured values was no greater than that between paired clearances. Factors for age and body weight must be included for reasonable prediction.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Interstitial lung disease in Japanese patients with lung cancer: a cohort and nested case-control study.

            Interstitial lung disease (ILD) occurs in Japanese patients with non-small cell lung cancer (NSCLC) receiving gefitinib. To elucidate risk factors for ILD in Japanese patients with NSCLC during treatment with gefitinib or chemotherapy. In a prospective epidemiologic cohort, 3,166 Japanese patients with advanced/recurrent NSCLC were followed for 12 weeks on 250 mg gefitinib (n = 1,872 treatment periods) or chemotherapy (n = 2,551). Patients who developed acute ILD (n = 122) and randomly selected control subjects (n = 574) entered a case-control study. Adjusted incidence rate ratios were estimated from case-control data by odds ratios (ORs) with 95% confidence intervals (CIs) using logistic regression. Crude (observed) incidence rates and risks were calculated from cohort data. The observed (unadjusted) incidence rate over 12 weeks was 2.8 (95% CI, 2.3-3.3) per 1,000 person-weeks, 4.5 (3.5-5.4) for gefitinib versus 1.7 (1.2-2.2) for chemotherapy; the corresponding observed naive cumulative incidence rates at the end of 12-week follow-up were 4.0% (3.0-5.1%) and 2.1% (1.5-2.9%), respectively. Adjusted for imbalances in risk factors between treatments, the overall OR for gefitinib versus chemotherapy was 3.2 (1.9-5.4), elevated chiefly during the first 4 weeks (3.8 [1.9-7.7]). Other ILD risk factors in both groups included the following: older age, poor World Health Organization performance status, smoking, recent NSCLC diagnosis, reduced normal lung on computed tomography scan, preexisting chronic ILD, concurrent cardiac disease. ILD-related deaths in patients with ILD were 31.6% (gefitinib) versus 27.9% (chemotherapy); adjusted OR, 1.05 (95% CI, 0.3-3.2). ILD was relatively common in these Japanese patients with NSCLC during therapy with gefitinib or chemotherapy, being higher in the older, smoking patient with preexisting ILD or poor performance status. The risk of developing ILD was higher with gefitinib than chemotherapy, mainly in the first 4 weeks.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Severe acute interstitial pneumonia and gefitinib.

              Gefitinib is an oral selective inhibitor of the epidermal growth factor receptor tyrosine kinase that is an effective treatment for patients with advanced non-small cell lung cancer who do not respond to platinum-based chemotherapy. We assessed four patients who had non-small cell lung cancer causing severe acute interstitial pneumonia in association with gefitinib. Although two patients recovered after treatment with steroids, the other two died from progressive respiratory dysfunction. On the basis of autopsies and bilateral distribution of diffuse ground-glass opacities in chest CTs, we diagnosed diffuse alveolar damage, which was consistent with acute interstitial pneumonia. Patients with interstitial pneumonia also had other pulmonary disorders such as previous thoracic irradiation and poor performance status. Physicians should be aware of the alveolar damage induced by gefitinib, especially for patients with these characteristic features.
                Bookmark

                Author and article information

                Contributors
                +81-3-5363-3847 , tanigawara-yusuke@umin.ac.jp
                Journal
                Cancer Chemother Pharmacol
                Cancer Chemother. Pharmacol
                Cancer Chemotherapy and Pharmacology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0344-5704
                1432-0843
                14 February 2019
                14 February 2019
                2019
                : 83
                : 5
                : 849-858
                Affiliations
                [1 ]ISNI 0000 0004 0376 5631, GRID grid.476017.3, Clinical Pharmacology & Drug Safety and Metabolism Department, Science & Data Technology Division, , R&D, AstraZeneca K.K., ; Osaka, Japan
                [2 ]ISNI 0000 0004 0376 5631, GRID grid.476017.3, Statistics Group, Science & Data Technology Division, , R&D, AstraZeneca K.K., ; Osaka, Japan
                [3 ]ISNI 0000 0004 5929 4381, GRID grid.417815.e, Quantitative Clinical Pharmacology, Early Clinical Development, IMED Biotech Unit, , AstraZeneca, ; Cambridge, UK
                [4 ]GRID grid.418152.b, Quantitative Clinical Pharmacology, Early Clinical Development, IMED Biotech Unit, , AstraZeneca, ; Gaithersburg, MD USA
                [5 ]ISNI 0000 0001 1519 6403, GRID grid.418151.8, Epidemiology, , AstraZeneca R&D, ; Mölndal, Sweden
                [6 ]Immuno-Oncology, Global Medicines Development, AstraZeneca R&D, Gaithersburg, MD USA
                [7 ]ISNI 0000 0004 1936 9959, GRID grid.26091.3c, Department of Clinical Pharmacokinetics and Pharmacodynamics, , Keio University School of Medicine, ; 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 Japan
                Article
                3788
                10.1007/s00280-019-03788-4
                6458983
                30762084
                d48b854e-8a44-4f4a-9c6c-044b8beed409
                © 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.

                History
                : 4 November 2018
                : 29 January 2019
                Funding
                Funded by: AZ IRESSA
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2019

                Oncology & Radiotherapy
                gefitinib,population pharmacokinetics,exposure-safety,interstitial lung disease,α1-acid glycoprotein

                Comments

                Comment on this article