Predictive factors of gefitinib antitumor activity in East Asian advanced non-small cell lung cancer patients

被引:59
作者
Chang, Gee-Chen
Tsai, Chun-Ming
Chen, Kun-Chieh
Yu, Chong-Jen
Shih, Jin-Yuan
Yang, Tsung-Ying
Lin, Ching-Pei
Hsu, Jeng-Yuan
Chiu, Chao-Hua
Perng, Reury-Perng
Yang, Pan-Chyr
Yang, Chih-Hsin
机构
[1] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[2] Taichung Vet Gen Hosp, Dept Internal Med, Div Chest Med, Taichung, Taiwan
[3] China Med Univ, Sch Med, Taichung, Taiwan
[4] Taipei Vet Gen Hosp, Chest Dept, Taipei, Taiwan
[5] Natl Yang Ming Univ, Sch Med, Dept Med, Taipei 112, Taiwan
[6] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[7] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
[8] Natl Chung Hsing Univ, Inst Biomed Sci, Taichung 40227, Taiwan
关键词
gefitinib; non-small cell lung cancer; predictive factor; chemonaive; performance status;
D O I
10.1097/01243894-200607000-00004
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Gender, smoking history, adenocarcinoma histology, performance status, and East Asian ethnicity were predictive factors of gefitinib response in previous analysis. However, these factors tend to be correlated with each other; it is not clear whether gender, smoking history, and adenocarcinoma histology were all independent predictors for response in East Asian populations. Methods: Tumor response, survival and predictive factors of gefitinib response of advanced non-small cell lung cancer patients treated between May of 2002 and November of 2004 were collected retrospectively from three medical centers in Taiwan. Univariate and multivariate logistic regression models were used to test potential predictive factors associated with response to gefitinib. Overall survivals between groups with different predictive factors were compared by log-rank tests. Multivariate analyses were performed to identify factors that independently predict for survival. Results: A total of 428 patients were analyzed. The median follow-up duration for living patients was 19.5 months (range, 10.2-39.9). Objective tumor response was observed in 114 patients (26.6%, 95% confidence interval [CI]: 22.4%-30.8%) and disease stabilization in 129 patients (30.2%). Response rate was statistically significant higher in adenocarcinoma, good performance status, and chemonaive patients in multivariate analysis. The median survival was 7.4 months (95% CI: 5.8-9.0) and 1-year survival was 34.3% (95% CI: 29.0%-38.0%). Significant independent predictive factors associated with longer survival in multivariate analysis were good performance status (p < 0.001) and responsiveness to gefitinib (p < 0.001). In 286 chemotherapy-treated patients, the response rate was 22.7%. Median and 1-year survival was 7.9 months and 36.7%, respectively. Good performance status was predictive of tumor response (p < 0.001) and better survival (p < 0.001) in multivariate analysis. Response to gefitinib was predictive of better survival (p < 0.001). Conclusions: Gender and smoking status were not, but good performance status (PS), no previous chemotherapy, and adenocarcinoma histology were independent predictive factors in multivariate analysis for gefitinib response in Taiwanese advanced non-small cell lung cancer population. In patients previously treated with chemotherapy, only good PS was an independent predictor for tumor response in multivariate analysis.
引用
收藏
页码:520 / 525
页数:6
相关论文
共 48 条
[1]
Gefitinib as first-line, compassionate use therapy in patients with advanced non-small-cell lung cancer [J].
Argiris, A ;
Mittal, N .
LUNG CANCER, 2004, 43 (03) :317-322
[2]
BRACONI C, 2003, P AM SOC CLIN ONCOL, V22
[3]
Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer [J].
Cappuzzo, F ;
Hirsch, FR ;
Rossi, E ;
Bartolini, S ;
Ceresoli, GL ;
Bemis, L ;
Haney, J ;
Witta, S ;
Danenberg, K ;
Domenichini, I ;
Ludovini, V ;
Magrini, E ;
Gregorc, V ;
Doglioni, C ;
Sidoni, A ;
Tonato, M ;
Franklin, WA ;
Crino, L ;
Bunn, PA ;
Varella-Garcia, M .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (09) :643-655
[4]
CAVINA R, 2003, LUNG CANCER, V41, pS248
[5]
Complications of therapy in cancer patients - Case 1. Paronychia and skin hyperpigmentation induced by gefitinib in advanced non-small-cell lung cancer [J].
Chang, GC ;
Yang, TY ;
Chen, KC ;
Yin, MC ;
Wang, RC ;
Lin, YC .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (22) :4646-4648
[6]
Gefitinib is active in patients with brain metastases from non-small cell lung cancer and response is related to skin toxicity [J].
Chiu, CH ;
Tsai, CM ;
Chen, YM ;
Chiang, SC ;
Liou, JL ;
Perng, RP .
LUNG CANCER, 2005, 47 (01) :129-138
[7]
Mutation in the tyrosine kinase domain of epidermal growth factor receptor is a predictive and prognostic factor for gefitinib treatment in patients with non-small cell lung cancer [J].
Chou, TY ;
Chiu, CH ;
Li, LH ;
Hsiao, CY ;
Tzen, CY ;
Chang, KT ;
Chen, YM ;
Perng, RP ;
Tsai, SF ;
Tsai, CM .
CLINICAL CANCER RESEARCH, 2005, 11 (10) :3750-3757
[8]
COPIN M, 2003, P AM SOC CLIN ONCOL, V22
[9]
DICKSON NR, 2004, P AN M AM SOC CLIN, V23, P634
[10]
Fossella FV, 1997, SEMIN ONCOL, V24, P455