Targeted therapy in lung cancer: IPASS and beyond, keeping abreast of the explosion of targeted therapies for lung cancer

被引:56
作者
Savas, Peter [1 ]
Hughes, Brett [2 ,3 ]
Solomon, Benjamin [1 ]
机构
[1] Peter MacCallum Canc Ctr, East Melbourne, Vic 3002, Australia
[2] Royal Brisbane & Womens Hosp, Herston, Qld, Australia
[3] Prince Charles Hosp, Chermside, Qld, Australia
关键词
Non-small-cell lung carcinoma (NSCLC); molecular targeted therapy; immunotherapy; epidermal growth factor receptor (EGFR); anaplastic lymphoma kinase (ALK); TYROSINE KINASE INHIBITOR; EML4-ALK FUSION GENE; BLIND PHASE-III; PREVIOUSLY TREATED PATIENTS; ANAPLASTIC LYMPHOMA KINASE; OPEN-LABEL; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT; RANDOMIZED MULTICENTER; CARBOPLATIN-PACLITAXEL;
D O I
10.3978/j.issn.2072-1439.2013.08.52
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Advances in the treatment of non-small cell lung cancer (NSCLC) over the last decade have predominantly involved the development of therapies directed at molecular targets such as mutations in the epidermal growth factor receptor (EGFR) or rearrangements in the anaplastic lymphoma kinase (ALK) gene. Other targets have been discovered at low frequency, with multiple agents approved or in development for treatment of these rare molecular subtypes. The tumour microenvironment has also provided opportunities for therapies targeting angiogenesis and the host immune response. This review will provide an overview of current targeted therapies in NSCLC and promising treatment approaches on the horizon.
引用
收藏
页码:S579 / S592
页数:14
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