EGFR targeting therapies: Monoclonal antibodies versus tyrosine kinase inhibitors similarities and differences

被引:102
作者
Dassonville, Olivier [1 ]
Lozec, Alexandre [1 ]
Fischel, Jean Louis [1 ]
Milano, Gerard [1 ]
机构
[1] Ctr Antoine Lacassagne, Lab Oncopharmacol, F-06189 Nice, France
关键词
EGFR; targeted therapy; monoclonal antibodies; tyrosine kinase inhibitors;
D O I
10.1016/j.critrevonc.2006.12.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Current development of targeted therapy in oncology is particularly active and concerns principally two types of agents which are monoclonal antibodies (Mabs) and tyrosine kinase inhibitors (TKIs). Epidermal growth factor receptor (EGFR) signaling pathways play a key role in the regulation of cell proliferation, survival and differentiation. Consequently, EGFR is one of the most-studied ligand-receptor systems and specific EGFR inhibition approaches are currently among the most promising and the most advanced in the clinical setting. Cetuximab (Erbitux((R))), belonging to the Mabs family, gefitinib (Iressa((R))) and erlotinib (Tarceva((R))), belonging to the TKIs family, are among the most advanced anti-EGFR drugs at the clinical level. The aim of this review article is to compare at both experimental and clinical levels the key points which govern the activity of these two types of targeting agents. (c) 2007 Published by Elsevier Ireland Ltd.
引用
收藏
页码:53 / 61
页数:9
相关论文
共 107 条
[1]   Pharmacodynamic studies with the epidermal growth factor receptor tyrosine kinase inhibitor ZD1839 [J].
Albanell, J ;
Rojo, F ;
Baselga, J .
SEMINARS IN ONCOLOGY, 2001, 28 (05) :56-66
[2]  
Aoji K, 1994, Nihon Jibiinkoka Gakkai Kaiho, V97, P41
[3]  
Arteaga CL, 2003, CLIN CANCER RES, V9, P1231
[4]  
Arteaga CL, 2001, J CLIN ONCOL, V19, p32S
[5]   Physical interaction between epidermal growth factor receptor and DNA-dependent protein kinase in mammalian cells [J].
Bandyopadhyay, D ;
Mandal, M ;
Adam, L ;
Mendelsohn, J ;
Kumar, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (03) :1568-1573
[6]   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
[7]   Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors [J].
Bianco, R ;
Shin, I ;
Ritter, CA ;
Yakes, FM ;
Basso, A ;
Rosen, N ;
Tsurutani, J ;
Dennis, PA ;
Mills, GB ;
Arteaga, CL .
ONCOGENE, 2003, 22 (18) :2812-2822
[8]   Key cancer cell signal transduction pathways as therapeutic targets [J].
Bianco, RB ;
Melisi, D ;
Ciardiello, F ;
Tortora, G .
EUROPEAN JOURNAL OF CANCER, 2006, 42 (03) :290-294
[9]   Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck [J].
Bonner, JA ;
Harari, PM ;
Giralt, J ;
Azarnia, N ;
Shin, DM ;
Cohen, RB ;
Jones, CU ;
Sur, R ;
Raben, D ;
Jassem, J ;
Ove, R ;
Kies, MS ;
Baselga, J ;
Youssoufian, H ;
Amellal, N ;
Rowinsky, EK ;
Ang, KK .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :567-578
[10]  
Bos M, 1997, CLIN CANCER RES, V3, P2099