Lung Cancer Genomics in the Era of Accelerated Targeted Drug Development

被引:8
作者
Wijesinghe, Priyanga [1 ]
Bollig-Fischer, Aliccia [1 ]
机构
[1] Wayne State Univ, Dept Oncol, Barbara Ann Karmanos Canc Inst, 4100 John R, Detroit, MI 48201 USA
来源
LUNG CANCER AND PERSONALIZED MEDICINE: NOVEL THERAPIES AND CLINICAL MANAGEMENT | 2016年 / 890卷
关键词
Lung cancer; Targeted therapy; Genomics; Tyrosine-kinase inhibitors; Molecular biomarkers; Fusion genes; Drug resistance; EGFR; ALK; GROWTH-FACTOR-RECEPTOR; SQUAMOUS-CELL CARCINOMA; GENE COPY NUMBER; PHASE-II TRIAL; TYROSINE KINASE INHIBITOR; EML4-ALK FUSION GENE; ACQUIRED-RESISTANCE; SOMATIC MUTATIONS; NEVER-SMOKERS; STANDARD CHEMOTHERAPY;
D O I
10.1007/978-3-319-24932-2_1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lung cancer is the leading cause of cancer-related deaths in the United States and the 5-year overall survival outlook for a patient has not improved in several decades. Recently, however, molecular and genomic profiling of the lung tumors has revealed recurring somatic mutations. As a result the therapeutic landscape of lung cancer is undergoing a paradigm shift from a purely histology-based understanding of the disease to subtype distinctions based on tumor genetics, which has launched cancer-specific, mechanism-based targeted therapies with clear benefit to patients. While targeted therapy advancements are being made at an ever increasing rate, a new challenge in the form of drug resistance has also emerged. This review summarizes the current literature for these issues.
引用
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页码:1 / 23
页数:23
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