Predictive factors for interstitial lung disease, antitumor response, and survival in non-small-cell lung cancer patients treated with gefitinib

被引:304
作者
Ando, M [1 ]
Okamoto, I
Yamamoto, N
Takeda, K
Tamura, K
Seto, T
Ariyoshi, Y
Fukuoka, M
机构
[1] Kyoto Univ, Sch Publ Hlth, Dept Prevent Serv, Hlth Serv,Sakyo Ku, Kyoto 6068501, Japan
[2] Kinki Univ, Sch Med, Dept Med Oncol, Osaka 589, Japan
[3] Osaka City Gen Hosp, Dept Clin Oncol, Osaka, Japan
[4] Shizuoka Canc Ctr, Div Thorac Oncol, Shizuoka, Japan
[5] Kinki Univ, Sch Med, Nara Hosp, Dept Med Oncol, Nara, Japan
[6] Tokai Univ, Sch Med, Div Med Oncol, Isehara, Kanagawa 25911, Japan
[7] Aichi Hosp, Aichi Canc Ctr, Aichi, Japan
关键词
D O I
10.1200/JCO.2005.04.9866
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Interstitial lung disease (ILD) is a serious adverse effect of gefitinib, but its prevalence and risk factors remain largely unknown. We examined the prevalence of and risk factors for gefitinib-induced ILD associated with practical use of the drug in Japanese with non-small-cell lung cancer (NSCLC). Patients and Methods Clinical information was retrospectively assembled for NSCLC patients who started gefitinib treatment at affiliated institutions of the West Japan Thoracic Oncology Group between August 31 and December 31, 2002. Medical records of patients who developed pulmonary infiltrates were reviewed by a central committee of extramural experts for identification of patients with gefitinib-induced ILD. Multivariate logistic or Cox regression analysis was performed to identify independent predictive factors for ILD, antitumor response, and survival. Results Seventy cases of and 31 deaths from gefitinib-induced ILD were identified among 1,976 consecutively corresponding to a prevalence of 3.5% and mortality of 1.6%. treated patients at 84 institutions, Gefitinib-induced ILD was significantly associated with male sex, a history of smoking, and coincidence of interstitial pneumonia (odds ratios = 3.10, 4.79, and 2.89, respectively). Predictive factors for adenocarcinoma histology, metastatic disease, and no history of smoking response were female sex,, good performance status (PS), whereas predictive factors for survival were female sex, no history of smoking, adenocarcinoma histology, nonmetastatic disease, good PS, and previous chest surgery. Conclusion ILD is a serious adverse effect of gefitinib in the clinical setting that cannot be ignored. However, patient selection based on sex and smoking history can minimize ILD risk and maximize the clinical benefit of gefitinib.
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页码:2549 / 2556
页数:8
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