Molecular Profiling to Optimize Treatment in Non-Small Cell Lung Cancer: A Review of Potential Molecular Targets for Radiation Therapy by the Translational Research Program of the Radiation Therapy Oncology Group

被引:30
|
作者
Ausborn, Natalie L. [2 ]
Quynh Thu Le [3 ]
Bradley, Jeffrey D. [4 ]
Choy, Hak [5 ]
Dicker, Adam P.
Saha, Debabrata [5 ]
Simko, Jeff [6 ]
Story, Michael D. [5 ]
Torossian, Artour [2 ]
Lu, Bo [1 ]
机构
[1] Thomas Jefferson Univ, Dept Radiat Oncol, Jefferson Med Coll, Bodine Ctr, Philadelphia, PA 19107 USA
[2] Vanderbilt Univ, Sch Med, Dept Radiat Oncol, Nashville, TN 37212 USA
[3] Stanford Univ, Dept Radiat Oncol, Palo Alto, CA 94304 USA
[4] Washington Univ, Dept Radiat Oncol, Sch Med, St Louis, MO USA
[5] Univ Texas SW Med Ctr Dallas, Dept Radiat Oncol, Dallas, TX 75390 USA
[6] Univ Calif San Francisco, Dept Urol, San Francisco, CA USA
关键词
Non-small cell lung cancer; Genomic signatures; Molecular markers; Radiation therapy; Chemotherapy; GENE-EXPRESSION PROFILES; ALBUMIN-BOUND PACLITAXEL; TRIPLE ANGIOKINASE INHIBITOR; PHASE-II TRIAL; SQUAMOUS-CELL; KINASE INHIBITION; DRUG-RESISTANCE; SOLID TUMORS; BIBF; 1120; ADENOCARCINOMA;
D O I
10.1016/j.ijrobp.2012.01.056
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Therapeutic decisions in non-small cell lung cancer (NSCLC) have been mainly based on disease stage, performance status, and co-morbidities, and rarely on histological or molecular classification. Rather than applying broad treatments to unselected patients that may result in survival increase of only weeks to months, research efforts should be, and are being, focused on identifying predictive markers for molecularly targeted therapy and determining genomic signatures that predict survival and response to specific therapies. The availability of such targeted biologics requires their use to be matched to tumors of corresponding molecular vulnerability for maximum efficacy. Molecular markers such as epidermal growth factor receptor (EGFR), K-ras, vascular endothelial growth factor (VEGF), mammalian target of rapamycin (mTOR), and anaplastic lymphoma kinase (ALK) represent potential parameters guide treatment decisions. Ultimately, identifying patients who will respond to specific therapies will allow optimal efficacy with minimal toxicity, which will result in more judicious and effective application of expensive targeted therapy as the new paradigm of personalized medicine develops. (C) 2012 Elsevier Inc.
引用
收藏
页码:E453 / E464
页数:12
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