Current and Future Molecular Testing in NSCLC, What Can We Expect from New Sequencing Technologies?

被引:45
作者
Garinet, Simon [1 ,2 ]
Laurent-Puig, Pierre [1 ,2 ]
Blons, Helene [1 ,2 ]
Oudart, Jean-Baptiste [2 ]
机构
[1] Paris Sorbonne Cite Univ, INSERM UMR S1147, F-75270 Paris 06, France
[2] Georges Pompidou European Hosp, AP HP, Dept Biochem, Unit Pharmacogenet & Mol Oncol, F-75015 Paris, France
关键词
lung cancer; molecular analysis; NGS; oncogene drivers; CELL LUNG-CANCER; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITORS; UNCOMMON EGFR MUTATIONS; OPEN-LABEL; 1ST-LINE TREATMENT; CLINICAL ONCOLOGY; PD-L1; EXPRESSION; TARGETED THERAPY; LIQUID BIOPSY;
D O I
10.3390/jcm7060144
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent changes in lung cancer care, including new approvals in first line and the introduction of high-throughput molecular technologies in routine testing led us to question ourselves on how deeper molecular testing may be helpful for the optimal use of targeted drugs. In this article, we review recent results in the scope of personalized medicine in lung cancer. We discuss biomarkers that have a therapeutic predictive value in lung cancer with a focus on recent changes and on the clinical value of large scale sequencing strategies. We review the use of second- and third-generation EGFR and ALK inhibitors with a focus on secondary resistance alterations. We discuss anti-BRAF and anti-MEK combo, emerging biomarkers as NRG1 and NTRKs fusions and immunotherapy. Finally, we discuss the different technical issues of comprehensive molecular profiling and show how large screenings might refine the prediction value of individual markers. Based on a review of recent publications (2012-2018), we address promising approaches for the treatment of patients with lung cancers and the technical challenges associated with the identification of new predictive markers.
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页数:23
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