Personalized medicine in non-small cell lung cancer: a review from a pharmacogenomics perspective

被引:44
|
作者
Jiang, Wenxiao [1 ]
Cai, Guiqing [1 ]
Hu, Peter C. [2 ]
Wang, Yue [3 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[2] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
Personalized medicine; Non-small cell lung cancer; Pharmacogenomics; Tyrosine kinase; Anaplastic lymphoma kinase; Inhibitor; Monoclonal antibody; ACUTE PROMYELOCYTIC LEUKEMIA; TRANS-RETINOIC ACID; TYROSINE KINASE INHIBITORS; ACQUIRED-RESISTANCE; ARSENIC TRIOXIDE; EGFR MUTATIONS; OPEN-LABEL; CLINICAL RESISTANCE; ALK INHIBITORS; PD-1; BLOCKADE;
D O I
10.1016/j.apsb.2018.04.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-small cell lung cancer is a prevalent and rapidly-expanding challenge to modern medicine. While generalized medicine with traditional chemotherapy yielded comparatively poor response rates and treatment results, the cornerstone of personalized medicine using genetic profiling to direct treatment has exalted the successes seen in the field and raised the standard for patient treatment in lung and other cancers. Here, we discuss the current state and advances in the field of personalized medicine for lung cancer, reviewing several of the mutation-targeting strategies that are approved for clinical use and how they are guided by patient genetic information. These classes include inhibitors of tyrosine kinase (TKI), anaplastic lymphoma kinase (ALK), and monoclonal antibodies. Selecting from these treatment plans and determining the optimal dosage requires in-depth genetic guidance with consideration towards not only the underlying target genes but also other factors such as individual metabolic capability and presence of resistance-conferring mutations both directly on the target gene and along its cascade(s). Finally, we provide our viewpoints on the future of personalized medicine in lung cancer, including target-based drug combination, mutation-guided drug design and the necessity for data of population genetics, to provide rough guidance on treating patients who are unable to get genetic testing. (C) 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:530 / 538
页数:9
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