Publication: Gefitinib-Related Interstitial Lung Disease in Taiwanese Patients With Non-Small-Cell Lung Cancer
dc.contributor | 臺大醫院-內科部; | en |
dc.contributor.author | Chang, Shih-Chieh | en |
dc.contributor.author | Chang, Cheng-Yu | en |
dc.contributor.author | Chang, Shu-Ju | en |
dc.contributor.author | Yuan, Mei-Kang | en |
dc.contributor.author | Lai, Yi-Chun | en |
dc.contributor.author | Liu, Yu-Chang | en |
dc.contributor.author | Chen, Cheng-Yu | en |
dc.contributor.author | Kuo, Li-Chiao | en |
dc.contributor.author | Yu, Chong-Jen | en |
dc.creator | Chang, Shih-Chieh;Chang, Cheng-Yu;Chang, Shu-Ju;Yuan, Mei-Kang;Lai, Yi-Chun;Liu, Yu-Chang;Chen, Cheng-Yu;Kuo, Li-Chiao;Yu, Chong-Jen | en |
dc.date | 2013 | en |
dc.date.accessioned | 2014-02-14T05:05:41Z | |
dc.date.accessioned | 2018-07-11T06:45:57Z | |
dc.date.available | 2014-02-14T05:05:41Z | |
dc.date.available | 2018-07-11T06:45:57Z | |
dc.date.issued | 2013 | |
dc.description.abstract | Gefitinib is effective in the treatment of non-small-cell lung cancer (NSCLC), especially in the Asian population. However, interstitial lung disease (ILD) is usually a serious pulmonary adverse effect. The incidence and clinical outcome of 1080 Taiwanese patients with advanced NSCLC who received gefitinib treatment was investigated. Taiwanese patients with NSCLC had a relatively high incidence (2.3%) of ILD with poor outcome (40% mortality) during gefitinib treatment. Background: Gefitinib (Iressa; AstreZeneca, Wilmington, DE) is effective in the treatment of NSCLC, especially in the Asian population. However, ILD is usually a serious pulmonary adverse effect and almost leads to cessation of gefitinib treatment. In this study, we investigated the incidence, clinical features, and prognosis of gefitinib-related ILD in Taiwanese patients with NSCLC. Patients and Methods: This was a retrospective observational study conducted in 2 medical centers and a local teaching hospital. Results: A total of 1080 patients with NSCLC, who received at least 1 dose (250 mg per day) of gefitinib treatment, were enrolled. Of these, 42 patients were diagnosed with ILD. Twenty-five of the 42 patients were diagnosed with gefitinib-related ILD (incidence, 2.3%). The main manifestations of ILD included dyspnea, cough, and hypoxemia. Six of the 25 patients (24%) with gefitinib-related ILD required invasive mechanical ventilation and all patients were treated with steroids. Twenty-two patients (88%) discontinued gefitinib treatment without further rechallenge. Ten (40%) patients died directly from ILD and in-hospital mortality was 52%. Eleven patients received subsequent cytotoxic chemotherapy with a mean of 33.5 days after ILD events. Kaplan-Meier analysis demonstrated that gefitinib nonresponder and gefitinib use rather than first-line treatment were associated with poor prognosis when ILD developed during gefitinib treatment. Conclusion: Taiwanese patients with NSCLC had a relatively high incidence of ILD during gefitinib treatment. Gefitinib-related ILD is usually life-threatening, especially in gefitinib nonresponders and gefitinib use rather than first-line treatment. Clinical Lung Cancer, Vol. 14, No. 1, 55-61 Crown Copyright (C) 2013 Published by Elsevier Inc. All rights reserved. | en |
dc.format.extent | 108 bytes | |
dc.format.mimetype | text/html | |
dc.identifier.uri | http://ntur.lib.ntu.edu.tw//handle/246246/259006 | |
dc.identifier.uri.fulltext | http://ntur.lib.ntu.edu.tw/bitstream/246246/259006/1/index.html | |
dc.language | en-us | en |
dc.relation | Clin. Lung Cancer, 14(1), 55-61 | en |
dc.relation.ispartof | Clin. Lung Cancer | |
dc.relation.journalissue | 1 | |
dc.relation.journalvolume | 14 | |
dc.relation.pages | 55-61 | |
dc.subject | Gefitinib | en |
dc.subject | Incidence | en |
dc.subject | Interstitial lung disease | en |
dc.subject | Non-small-cell lung cancer | en |
dc.subject | Outcome | en |
dc.subject.classification | [SDGs]SDG3 | |
dc.title | Gefitinib-Related Interstitial Lung Disease in Taiwanese Patients With Non-Small-Cell Lung Cancer | en |
dspace.entity.type | Publication |
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