Lung Cancer in the Era of Precision Medicine

被引:155
作者
Politi, Katerina [1 ,2 ,3 ]
Herbst, Roy S. [2 ,3 ]
机构
[1] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Med, Sect Med Oncol, New Haven, CT 06520 USA
[3] Yale Canc Ctr, New Haven, CT USA
关键词
K-RAS ONCOGENE; ACQUIRED-RESISTANCE; DRIVER MUTATIONS; EGFR INHIBITORS; GENE-MUTATIONS; CELL; ALK; CRIZOTINIB; ADENOCARCINOMA; GEFITINIB;
D O I
10.1158/1078-0432.CCR-14-2748
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The past decade has been transformative for lung cancer patients, physicians, and scientists. The discovery of EGFR mutations that confer sensitivity to tyrosine kinase inhibitors in lung adenocarcinomas in 2004 heralded the beginning of the era of precision medicine for lung cancer. Indeed, it precipitated concerted efforts by many investigators to define molecular subgroups of lung cancer, characterize the genomic landscape of lung cancer subtypes, identify novel therapeutic targets, and define mechanisms of sensitivity and resistance to targeted therapies. The fruits of these efforts are visible every day now in lung cancer clinics: Patients receive molecular testing to determine whether their tumor harbors an actionable mutation, new and improved targeted therapies that can over-come resistance to first-generation drugs are in clinical trials, and drugs targeting the immune system are showing activity in patients. This extraordinary promise is tempered by the sobering fact that even the newest treatments for metastatic disease are rarely curative and are effective only in a small fraction of all patients. Ongoing and future efforts to find new vulnerabilities of lung cancers, unravel the complexity of drug resistance, increase the efficacy of immunotherapies, and perform biomarker-driven clinical trials are necessary to improve outcomes for patients with lung cancer. (C)2015 AACR.
引用
收藏
页码:2213 / 2220
页数:8
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