Interstitial lung disease associated with gefitinib

被引:28
作者
Kataoka, K
Taniguchi, H
Hasegawa, Y [1 ]
Kondoh, Y
Kimura, T
Nishiyama, O
Imaizumi, K
Kawabe, T
Kume, H
Shimokata, K
机构
[1] Nagoya Univ, Grad Sch Med, Dept Med, Div Resp Med, Nagoya, Aichi 4668550, Japan
[2] Tosei Gen Hosp, Dept Resp Med & Allergy, Aichi, Japan
关键词
bronchoalveolar lavage; gefitinib; interferon-inducible protein-10; interstitial lung disease; non-small-cell lung cancer; thymus- and activation-regulated chemokine;
D O I
10.1016/j.rmed.2005.07.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although pulmonary toxicity associated with gefitinib, an epidermal growth factor receptor inhibitor, has been reported recently, the accumulation of clinical information and the underlying mechanisms of gefitinib-induced interstitial lung disease (ILD) remain insufficient and unclear. After retrospectively reviewing the clinical records and chest X-rays of 489 lung cancer patients who were treated with gefitinib, we diagnosed four cases of gefitinib-induced ILD who underwent fiberoptic bronchoscopy and bronchoalveolar lavage (BAL). We found that the period of time from starting gefitinib to the onset of ILD was short, and concluded that a careful and close observation of a chest imaging study and a collection of respiratory symptoms was recommended. All four patients were treated with a high dose of corticosteroids, and ILD was resolved. We detected high levels of interferon-inducible protein-10 in BAL fluid, although we could not demonstrate the characteristic features of laboratory findings or BAL fluid cell analysis. We speculated that a Th1 type of lung tissue inflammation or lung injury might be involved as a part of mechanisms underlying gefitinib-induced ILD. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:698 / 704
页数:7
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