Targeted Therapies for Lung Cancer Clinical Experience and Novel Agents

被引:93
作者
Larsen, Jill E. [1 ]
Cascone, Tina [2 ]
Gerber, David E. [3 ]
Heymach, John V. [2 ]
Minna, John D. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Hamon Ctr Therapeut Oncol Res, Simmons Canc Ctr, Dallas, TX 75390 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Head & Neck Med Oncol, Houston, TX 77030 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Hematol Oncol, Dallas, TX 75390 USA
关键词
Lung cancer; targeted therapies; genome-wide tumor analysis; tyrosine kinase inhibitor; monoclonal antibody; EGFR; VEGF; ALK; NONSMALL CELL LUNG; EPIDERMAL-GROWTH-FACTOR; FACTOR-RECEPTOR GENE; RANDOMIZED PHASE-II; PREVIOUSLY TREATED PATIENTS; TYROSINE KINASE; ACQUIRED-RESISTANCE; COPY NUMBER; STEM-CELLS; TELOMERASE ACTIVITY;
D O I
10.1097/PPO.0b013e31823e701a
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although lung cancer remains the leading cancer killer in the United States, recently a number of developments indicate future clinical benefit. These include evidence that computed tomography-based screening decreases lung cancer mortality, the use of stereotactic radiation for early-stage tumors, the development of molecular methods to predict chemotherapy sensitivity, and genome-wide expression and mutation analysis data that have uncovered oncogene "addictions" as important therapeutic targets. Perhaps the most significant advance in the treatment of this challenging disease is the introduction of molecularly targeted therapies, a term that currently includes monoclonal antibodies and small-molecule tyrosine kinase inhibitors. The development of effective targeted therapeutics requires knowledge of the genes and pathways involved and how they relate to the biologic behavior of lung cancer. Drugs targeting the epidermal growth factor receptor, anaplastic lymphoma kinase, and vascular endothelial growth factor are now U. S. Food and Drug Administration approved for the treatment of advanced non-small cell lung cancer. These agents are generally better tolerated than conventional chemotherapy and show dramatic efficacy when their use is coupled with a clear understanding of clinical data, mechanism, patient selection, drug interactions, and toxicities. Integrating genome-wide tumor analysis with drug-and targeted agent-responsive phenotypes will provide a wealth of new possibilities for lung cancer-targeted therapeutics. Ongoing research efforts in these areas as well as a discussion of emerging targeted agents being evaluated in clinical trials are the subjects of this review.
引用
收藏
页码:512 / 527
页数:16
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