Molecular analysis of cell-free circulating DNA for the diagnosis of somatic mutations associated with resistance to tyrosine kinase inhibitors in non-small-cell lung cancer

被引:15
作者
Del Re, Marzia [1 ]
Vasile, Enrico [2 ]
Falcone, Alfredo [2 ]
Danesi, Romano [1 ]
Petrini, Iacopo [2 ]
机构
[1] Univ Pisa, Clin Pharmacol Unit, Dept Clin & Expt Med, Pisa, Italy
[2] Univ Pisa, Med Oncol Unit, Dept Translat Res & New Technol Med & Surg, Pisa, Italy
关键词
circulating cell-free tumor DNA; EGFR; non-small-cell lung cancer; pharmacologic inhibitors; ALK; acquired resistance; GROWTH-FACTOR RECEPTOR; RANDOMIZED PHASE-II; ACQUIRED-RESISTANCE; MET AMPLIFICATION; EGFR MUTATIONS; MESENCHYMAL TRANSITION; GEFITINIB RESISTANCE; 1ST-LINE TREATMENT; DRUG-RESISTANCE; T790M MUTATIONS;
D O I
10.1586/14737159.2014.908120
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
In non-small-cell lung cancer, the molecular diagnosis of somatic mutations is instrumental for the choice of the most appropriate treatment. However, despite an initial response, resistance to tyrosine kinase inhibitors occurs and thereafter tumors progress. For this reason, next generation inhibitors able to overcome acquired resistances are currently in development. Therefore, the identification of the molecular determinants of resistance is needed to adapt treatment accordingly. The analysis of circulating cell-free tumor DNA represents a powerful tool to monitor the somatic changes induced by treatment. This review focuses on the most recent advantages in the diagnosis of acquired resistance in circulating cell-free tumor DNA and underlines the strategies ready to be translated in the clinical practice.
引用
收藏
页码:453 / 468
页数:16
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