Targeted agents in the treatment of lung cancer

被引:1
作者
Staudacher, L. [1 ,2 ]
Teixeira, L. [3 ,4 ]
Kempf, E. [1 ]
Rousseau-Bussac, G. [1 ]
Jouveshomme, S. [1 ]
Cohen, R. [1 ]
Beuzelin, C. [1 ]
Jagot, J. -L. [1 ]
Salmeron, S. [1 ]
Tredaniel, J. [1 ,2 ]
机构
[1] Hop St Joseph, Serv Pneumol, F-75014 Paris, France
[2] Univ Paris 05, F-75270 Paris 06, France
[3] Hop St Antoine, Serv Oncol Med, F-75571 Paris 12, France
[4] Univ Paris 06, F-75005 Paris, France
来源
PATHOLOGIE BIOLOGIE | 2012年 / 60卷 / 04期
关键词
Lung cancer; Targeted therapy; EGFR; Angiogenesis; Gefitinib; Erlotinib; Cetuximab; Bevacizumab; GROWTH-FACTOR RECEPTOR; PHASE-III TRIAL; PREVIOUSLY TREATED PATIENTS; GEMCITABINE PLUS CISPLATIN; 1ST-LINE THERAPY; INDUCTION CHEMOTHERAPY; TYROSINE KINASE; MAINTENANCE THERAPY; AMERICAN SOCIETY; SUPPORTIVE CARE;
D O I
10.1016/j.patbio.2012.05.011
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Lung cancer is in France, the leading cause of cancer death. Despite the dramatic advances that have allowed in a few years to go, for metastatic cancer, from a median survival without specific treatment of 4.5 months and now almost always more than one year, survival remains disappointing and further improvements are needed. Progress in the accumulated knowledge of the inner workings of normal and tumoral cells have paved the way for the development of targeted therapeutics called biological or simply targeted therapies. Two biological processes are already the target of marketed drugs, this is the way the receptor of epidermal growth factor (EGFR) and the path of neo-angiogenesis. It is almost assumed that, in the very near future, the inhibition of EML4-ALK will also be the subject of new drugs. In the medium term, it is conceivable that the molecular dissection of the tumors actually lead to the prescription of treatments tailored to mutations and other abnormalities that direct the growth of cancers. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:246 / 253
页数:8
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