Molecular Mechanism of EGFR-TKI Resistance in EGFR-Mutated Non-Small Cell Lung Cancer: Application to Biological Diagnostic and Monitoring

被引:57
|
作者
Reita, Damien [1 ,2 ]
Pabst, Lucile [3 ]
Pencreach, Erwan [1 ,4 ]
Guerin, Eric [1 ,4 ]
Dano, Laurent [1 ]
Rimelen, Valerie [1 ]
Voegeli, Anne-Claire [1 ]
Vallat, Laurent [1 ]
Mascaux, Celine [3 ,4 ]
Beau-Faller, Michele [1 ,4 ]
机构
[1] Strasbourg Univ Hosp, Dept Biochem & Mol Biol, F-67098 Strasbourg, France
[2] Strasbourg Univ, UMR CNRS 7021, Bioimagery & Pathol LBP, F-67400 Illkirch Graffenstaden, France
[3] Strasbourg Univ Hosp, Dept Pneumol, F-67091 Strasbourg, France
[4] Strasbourg Univ, INSERM U1113, IRFAC, F-67000 Strasbourg, France
关键词
EGFR mutations; non-small cell lung cancer; tyrosine kinase inhibitors; resistance mechanisms; molecular analysis; next-generation sequencing; cell-free DNA; TYROSINE KINASE INHIBITORS; FACTOR-RECEPTOR MUTATIONS; RANDOMIZED PHASE-II; OPEN-LABEL; ACQUIRED-RESISTANCE; ADVANCED NSCLC; 1ST-LINE TREATMENT; TARGETED-THERAPY; CARBOPLATIN-PACLITAXEL; CONFERS RESISTANCE;
D O I
10.3390/cancers13194926
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary: Non-small cell lung cancer (NSCLC) is the most common cancer in the world. For common EGFR mutations, treatment is based on different inhibitors. Despite the excellent disease control with inhibitors, acquired resistance inevitably occurs and remains a biological challenge. This leads to the discovery of novel biomarkers and some possible drug targets. Resistance mechanisms could be involved as gene mutations, amplifications or fusions, which could be detected by different molecular techniques on different types of biological samples. Histological transformation is another mechanism of resistance with some biological predictive factors that needs tumor biopsy. The place of liquid biopsy also depends on the generation/line of inhibitors and could be a good candidate for molecular monitoring. This article is based on the literature and proposes actual and future directions in clinical and translational research. Non-small cell lung cancer (NSCLC) is the most common cancer in the world. Activating epidermal growth factor receptor (EGFR) gene mutations are a positive predictive factor for EGFR tyrosine kinase inhibitors (TKIs). For common EGFR mutations (Del19, L858R), the standard first-line treatment is actually third-generation TKI, osimertinib. In the case of first-line treatment by first (erlotinib, gefitinib)- or second-generation (afatinib) TKIs, osimertinib is approved in second-line treatment for patients with T790M EGFR mutation. Despite the excellent disease control results with EGFR TKIs, acquired resistance inevitably occurs and remains a biological challenge. This leads to the discovery of novel biomarkers and possible drug targets, which vary among the generation/line of EGFR TKIs. Besides EGFR second/third mutations, alternative mechanisms could be involved, such as gene amplification or gene fusion, which could be detected by different molecular techniques on different types of biological samples. Histological transformation is another mechanism of resistance with some biological predictive factors that needs tumor biopsy. The place of liquid biopsy also depends on the generation/line of EGFR TKIs and should be a good candidate for molecular monitoring. This article is based on the literature and proposes actual and future directions in clinical and translational research.
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页数:43
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