Targeted therapies for advanced non-small-cell lung cancer: Current status and future implications

被引:54
作者
Custodio, Ana [1 ]
Mendez, Miriam [1 ]
Provencio, Mariano [1 ]
机构
[1] Hosp Univ Puerta de Hierro Majadahonda, Dept Med Oncol, Madrid 28222, Spain
关键词
Advanced non-small-cell lung cancer; Combining targeted therapies; Epidermal growth factor receptor inhibitors; Angiogenesis inhibitors; Multitargeted tyrosine quinase inhibitors; GROWTH-FACTOR RECEPTOR; HISTONE DEACETYLASE INHIBITOR; TYROSINE KINASE INHIBITOR; RANDOMIZED PHASE-II; SYNERGISTIC ANTITUMOR-ACTIVITY; VANDETANIB PLUS DOCETAXEL; GENE COPY NUMBER; PROTEASOME INHIBITOR; TUMOR-GROWTH; ACQUIRED-RESISTANCE;
D O I
10.1016/j.ctrv.2011.04.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer remains the leading cause of malignancy-related mortality worldwide, with over one million cases diagnosed yearly. Non-small-cell lung cancer (NSCLC) accounts for >80% of all lung cancers. Because lung cancer is typically diagnosed at an advanced stage, chemotherapy (CT) is the mainstay of management. Conventional treatment of NSCLC has apparently reached a plateau of effectiveness in improving survival of patients, and treatment outcomes must still be considered disappointing. Hence, considerable efforts have been made in order to identify novel targeted agents that interfere with other dysregulated pathways in advanced NSCLC patients. In order to further improve the results of targeted therapy, we should not forget that lung cancer is a heterogeneous disease with multiple mutations, and it is unlikely that any single signaling pathway drives the oncogenic behaviour of all tumours. The relative failure of some targeted therapies may be a result of multilevel cross-stimulation among the targets of the new biological agents along several pathways of signal transduction that lead to neoplastic events. Thus, blocking only one of these pathways allows others to act as salvage or escape mechanisms for cancer cells. We summarize the most promising research approaches to the treatment of NSCLC, with particular attention to drugs with multiple targets or combining targeted therapies. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:36 / 53
页数:18
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