Individualized therapy in non-small-cell lung cancer: future versus current clinical practice

被引:22
作者
Perez-Soler, R. [1 ]
机构
[1] Albert Einstein Coll Med, Montefiore Med Ctr, Dept Oncol, Div Med Oncol, Bronx, NY 10467 USA
关键词
EGFR; biomarker; genomics; proteomics; GROWTH-FACTOR RECEPTOR; MESSENGER-RNA EXPRESSION; BETA-TUBULIN GENE; ACQUIRED-RESISTANCE; ACTIVATING MUTATIONS; PROLONGED SURVIVAL; ERCC1; EXPRESSION; PREDICTIVE-VALUE; PHASE-III; GEFITINIB;
D O I
10.1038/onc.2009.200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite advances in the management of non-small-cell lung cancer (NSCLC), including the introduction of targeted therapies such as epidermal growth factor receptor tyrosine kinase inhibitors, improvements in survival are marginal and the overall prognosis for patients remains poor. Tailoring therapy to the individual patient is a promising approach for selecting the most appropriate therapeutic regimens to maximize efficacy and minimize toxicity. The identification of predictive biomarkers that can guide treatment decisions is an important step for individualized therapy and in ultimately improving patient outcomes. Genomic and proteomic studies provide a means for the molecular profiling of tumor tissue from patients with NSCLC, and allow tailoring of therapy whereby the most appropriate treatment is administered to each individual patient. Although there are still significant challenges to implementing genomic and proteomic testing in clinical practice, the rapid development of newer technologies provides hope for overcoming these barriers. Oncogene (2009) 28, S38-S45; doi:10.1038/onc.2009.200
引用
收藏
页码:S38 / S45
页数:8
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