Diffuse alveolar damage after ZD1839 therapy in a patient with non-small cell lung cancer

被引:63
作者
Okamoto, I
Fujii, K
Matsumoto, M
Terasaki, Y
Kihara, N
Kohrogi, H
Suga, M
机构
[1] Kumamoto Univ, Sch Med, Dept Internal Med 1, Kumamoto 8600811, Japan
[2] Kumamoto Univ, Sch Med, Dept Pathol 2, Kumamoto 8600811, Japan
关键词
EGFR tyrosine kinase inhibitor; ZD1839 (Iressa); pulmonary toxicity; diffuse alveolar damage;
D O I
10.1016/S0169-5002(03)00043-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ZD 1839 is an orally active inhibitor selective for the epidermal growth factor receptor tyrosine kinase and has shown promise in the treatment of non-small cell lung cancer (NSCLC). We now present a case of diffuse alveolar damage (DAD) that developed in a 67-year-old man treated with ZD1839. On day 8 of ZD1839 administration, the patient complained of dyspnea and a new-ground glass opacity was apparent on a chest X-ray and computed tomography scan. Despite high-dose steroid therapy, the patient died 13 days after the first administration of ZD1839. Postmortem analysis of lung tissue revealed a pattern of DAD. No evidence of infection or of other specific etiologies was apparent. This case is the first reported of respiratory failure after ZD1839 treatment in a patient with NSCLC. Physicians should therefore be aware of the potential pulmonary toxicity of ZD1839. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:339 / 342
页数:4
相关论文
共 13 条
[1]   Tyrosine kinase inhibitors-ZD1839 (Iressa) [J].
Arteaga, CL ;
Johnson, DH .
CURRENT OPINION IN ONCOLOGY, 2001, 13 (06) :491-498
[2]   Phase I safety, pharmacokinetic, and pharmacodynamic trial of ZD1839, a selective oral epidermal growth factor receptor tyrosine kinase inhibitor, in patients with five selected solid tumor types [J].
Baselga, J ;
Rischin, D ;
Ranson, M ;
Calvert, H ;
Raymond, E ;
Kieback, DG ;
Kaye, SB ;
Gianni, L ;
Harris, A ;
Bjork, T ;
Averbuch, SD ;
Feyereislova, A ;
Swaisland, H ;
Rojo, F ;
Albanell, J .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (21) :4292-4302
[3]   SHOCK LUNG AND DIFFUSE ALVEOLAR DAMAGE PATHOLOGICAL AND PATHOGENETIC CONSIDERATIONS [J].
BLENNERHASSETT, JB .
PATHOLOGY, 1985, 17 (02) :239-247
[4]  
Ciardiello F, 2001, CLIN CANCER RES, V7, P2958
[5]   Drugs that may injure the respiratory system [J].
Foucher, P ;
Biour, M ;
Blayac, JP ;
Godard, P ;
Sgro, C ;
Kuhn, M ;
Vergnon, JM ;
Vervloet, D ;
Pfitzenmeyer, P ;
Ollagnier, M ;
Mayaud, C ;
Camus, P .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (02) :265-279
[6]  
Fukuoka M., 2002, P AN M AM SOC CLIN, V21, p298a
[7]   Dose-related protection from nickel-induced lung injury in Transgenic mice expressing human transforming growth factor-α [J].
Hardie, WD ;
Prows, DR ;
Piljan-Gentle, A ;
Dunlavy, MR ;
Wesselkamper, SC ;
Leikauf, GD ;
Korfhagen, TR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 26 (04) :430-437
[8]  
HARDIE WD, 1999, AM J PHYSIOL, V277, P1045
[9]   Selective oral epidermal growth factor receptor tyrosine kinase inhibitor ZD1839 is generally well-tolerated and has activity in non-small-cell lung cancer and other solid tumors: Results of a phase I trial [J].
Herbst, RS ;
Maddox, AM ;
Small, EJ ;
Rothenberg, L ;
Small, EL ;
Rubin, EH ;
Baselga, J ;
Rojo, F ;
Hong, WK ;
Swaisland, H ;
Averbuch, SD ;
Ochs, J ;
LoRusso, PM .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (18) :3815-3825
[10]  
KATZENSTEIN ALA, 1976, AM J PATHOL, V85, P210