The role of targeted therapy in non-small cell lung cancer

被引:25
作者
Maione, P
Rossi, A
Airoma, G
Ferrara, C
Castaldo, V
Gridelli, C
机构
[1] SG Moscati Hosp, Unite Opert Oncol Med, I-83100 Avellino, Italy
[2] SG Moscati Hosp, Direz Sanitaria, I-83100 Avellino, Italy
关键词
non-small cell lung cancer; targeted therapy; new biological agents; gefitinib;
D O I
10.1016/j.critrevonc.2004.02.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The therapy of non-small cell lung cancer (NSCLC) has reached a plateau in improving patient survival, with overall disappointing results. Thus, clinical research for new treatment strategies is warranted. Advances in the singling out molecular targets for NSCLC treatment has granted the development of several new biological agents. In the present paper we describe the main clinical data currently available on targeted agents in the treatment of NSCLC, focusing on epidermal growth factor receptor family inhibitors, angiogenesis inhibitors, signal transduction inhibitors, eicosanoid pathway inhibitors, vaccines and gene therapy. Several targeted agents have been introduced into clinical trials in NSCLC, mainly in advanced disease, with the first phase III study results being recently made available. To date, few of these new agents can offer hope of a substantial impact on the natural history of NSCLC, and negative results are more commonly reported than positive ones. Nevertheless, clinically-meaningful advances have already been achieved in chemotherapy refractory advanced NSCLC patients, with gefitinib, an epidermal growth factor receptor tyrosine kinase inhibitor, representing a further chance of tumor control and symptom palliation. Moreover, important lessons can be learned from this first generation of clinical trials. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:29 / 44
页数:16
相关论文
共 138 条
[1]   Phase II study of the farnesyl transferase inhibitor r115777 in patients with advanced non-small-cell lung cancer [J].
Adjei, AA ;
Mauer, A ;
Bruzek, L ;
Marks, RS ;
Hillman, S ;
Geyer, S ;
Hanson, LJ ;
Wright, JJ ;
Erlichman, C ;
Kaufmann, SH ;
Vokes, EE .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (09) :1760-1766
[2]   Blocking oncogenic Ras signaling for cancer therapy [J].
Adjei, AA .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (14) :1062-1074
[3]  
Adjei AA, 2000, CANCER RES, V60, P1871
[4]   Celecoxib, a selective cyclo-oxygenase-2 inhibitor, enhances the response to preoperative paclitaxel and carboplatin in early-stage non-small-cell lung cancer [J].
Altorki, NK ;
Keresztes, RS ;
Port, JL ;
Libby, MD ;
Korst, RJ ;
Flieder, DB ;
Ferrara, CA ;
Yankelevitz, DF ;
Subbaramaiah, K ;
Pasmantier, MW ;
Dannenberg, AJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (14) :2645-2650
[5]  
[Anonymous], 2003, P AM SOC CLIN ONCOL
[6]   Growth control of lung cancer by interruption of 5-lipoxygenase-mediated growth factor signaling [J].
Avis, IM ;
Jett, M ;
Boyle, T ;
Vos, MD ;
Moody, T ;
Treston, AM ;
Martinez, A ;
Mulshine, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (03) :806-813
[7]  
BASELGA J, 2002, P AN M AM SOC CLIN, V21, P633
[8]  
BASSER R, 2001, P AN M AM SOC CLIN, V20, pA100
[9]  
Berardo MD, 1998, CANCER, V82, P1296, DOI 10.1002/(SICI)1097-0142(19980401)82:7<1296::AID-CNCR12>3.0.CO
[10]  
2-1