Targeted Therapies in Lung Cancer

被引:35
作者
Pirker, Robert [1 ]
Filipits, Martin [1 ]
机构
[1] Med Univ Vienna, Dept Med 1, A-1090 Vienna, Austria
关键词
Targeted therapy; EGFR; angiogenesis; growth factor receptors; lung cancer; GROWTH-FACTOR RECEPTOR; PHASE-II TRIAL; CHEMOTHERAPY-NAIVE PATIENTS; TRANSFERASE INHIBITOR R115777; PLATINUM-BASED CHEMOTHERAPY; PREVIOUSLY TREATED PATIENTS; COOPERATIVE-ONCOLOGY-GROUP; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; MONOCLONAL-ANTIBODY;
D O I
10.2174/138161209787002915
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Targeted therapies have improved and will continue to improve the outcome of lung cancer. Current strategies focus on the blockade of growth factor receptors and the inhibition of angiogenesis. Epidermal growth factor receptor (EGFR)-directed tyrosine kinase inhibitors (TKIs) have already been established as a treatment option in patients with advanced non-small cell lung cancer (NSCLC) progressing after prior treatment with chemotherapy. EGFR-directed monoclonal antibodies in combination with platinum-based first-line chemotherapy have shown promising efficacy in phase II trials. In a phase III trial, cetuximab combined with cisplatin/vinorelbine resulted in superior survival compared to chemotherapy alone in patients with advanced EGFR-positive NSCLC. Inhibition of angiogenesis has also been successfully applied as a new treatment strategy. Bevacizumab added to palliative chemotherapy has improved progression-free survival in two phase III trials and overall survival in one of these trials in selected patients with advanced non-squamous cell lung cancer. Bevacizumab is now approved for selected patients with advanced NSCLC in combination with platinum-based chemotherapy. Other targeted therapies including dual and multi-kinase inhibitors are in earlier stages of clinical development. In small cell lung cancer (SCLC), targeted therapies have also been studied but no clinical benefit could be demonstrated for these agents.
引用
收藏
页码:188 / 206
页数:19
相关论文
共 133 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]   An overview of farnesyltransferase inhibitors and their role in lung cancer therapy [J].
Adjei, AA .
LUNG CANCER, 2003, 41 :S55-S62
[3]  
ALBERTI W, 1995, BRIT MED J, V311, P899
[4]  
Amendt Christiane, 2003, Proceedings of the American Association for Cancer Research Annual Meeting, V44, P1234
[5]  
[Anonymous], J CLIN ONCOL
[6]  
[Anonymous], EUR RESP MON
[7]   Cisplatin-versus carboplatin-based chemotherapy in first-line treatment of advanced non-small-cell lung cancer: An individual patient data meta-analysis [J].
Ardizzoni, Andrea ;
Boni, Luca ;
Tiseo, Marcello ;
Fossella, Frank V. ;
Schiller, Joan H. ;
Paesmans, Marianne ;
Radosavljevic, Davorin ;
Paccagnella, Adriano ;
Zatloukal, Petr ;
Mazzanti, Paola ;
Bisset, Donald ;
Rosell, Rafael .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (11) :847-857
[8]  
Arnold AM, 2007, J CLIN ONCOL, V25, P4278, DOI 10.1200/JCO.2007.12.3083
[9]  
BELANI CP, 2007, J CLIN ONCOL, V25
[10]   Epidermal growth factor receptor mutations and gene amplification in non-small-cell lung cancer: Molecular analysis of the IDEAL/INTACT gefitinib trials [J].
Bell, DW ;
Lynch, TJ ;
Haserlat, SM ;
Harris, PL ;
Okimoto, RA ;
Brannigan, BW ;
Sgroi, DC ;
Muir, B ;
Riemenschneider, MJ ;
Iacona, RB ;
Krebs, AD ;
Johnson, DH ;
Giaccone, G ;
Herbst, RS ;
Manegold, C ;
Fukuoka, M ;
Kris, MG ;
Baselga, J ;
Ochs, JS ;
Haber, DA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (31) :8081-8092