Personalized Treatment of Lung Cancer

被引:46
作者
Salgia, Ravi [1 ]
Hensing, Thomas
Campbell, Nicholas
Salama, April K.
Maitland, Michael
Hoffman, Philip
Villaflor, Victoria
Vokes, Everett E.
机构
[1] Univ Chicago, Hematol Oncol Sect, Dept Med, Chicago, IL 60637 USA
关键词
GROWTH-FACTOR-RECEPTOR; PHASE-III TRIAL; SQUAMOUS-CELL CARCINOMA; GENE COPY NUMBER; 1ST-LINE TAXANE/CARBOPLATIN; ACQUIRED-RESISTANCE; PLUS CHEMOTHERAPY; RAS ONCOGENE; TUMOR-CELLS; C-MET;
D O I
10.1053/j.seminoncol.2011.01.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is a heterogenous group of disorders, and a difficult disease to treat. The traditional approach of surgical resection for early-stage disease, potentially followed by chemotherapy, as well chemotherapy (with or without radiation) in later stages of disease is being supplemented with a personalized approach. The personalized approach has classically been used by the oncologist based on clinical/pathological parameters such as the performance status of the patient and histology of lung cancer. As molecular mechanisms have been explored in lung cancer more recently, the personalized approach also has incorporated molecular abnormalities. In particular, EGFR, K-ras, ALK, MET, CBL, and COX2, have come to the forefront as potential biomarkers and therapeutic targets. Thus, we review the various molecular mechanisms in lung cancer and the role of novel therapeutics. © 2011 Elsevier Inc.
引用
收藏
页码:274 / 283
页数:10
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