The Value of Population Screening in Advancing Personalized Medicine in the Field of Lung Cancer.

Pharmacogenomics and Personalized Medicine Pub Date : 2021-08-14 eCollection Date: 2021-01-01 DOI:10.2147/PGPM.S267437
Alice Mogenet, Laurent Greillier, Pascale Tomasini
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引用次数: 2

Abstract

During the past decade, progress has been made in the field of lung cancer molecular biology and onco-immunology, leading to prolonged survival of patients. The combination of increased fundamental knowledge and the pharmaceutical pipeline has allowed the development of various tyrosine kinase inhibitors, targeting numerous molecular alterations. These drugs are now available in daily practice and have transformed survival outcomes for patients harboring EGFR, ALK or ROS1 alterations. Multiple clinical trials are now ongoing in order to increase the number of approved drugs, thus overcoming the issues of rare mutations and tyrosine kinase inhibitors resistance. Immune checkpoint inhibitors development has also changed lung cancer outcomes, but underwhelming response rates highlight the need for immune biomarkers. While PD-L1 expression was the first approved immune biomarker, it has shown several limitations and new biomarkers have to be identified to predict response or resistance to immune checkpoint inhibitors. Testing methods, molecular results and targeted therapeutic schedules will be harmonized in the coming years, with the help of dedicated molecular multidisciplinary boards.

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人群筛查在肺癌领域推进个体化医疗中的价值
在过去的十年中,肺癌分子生物学和肿瘤免疫学领域取得了进展,延长了患者的生存期。增加的基础知识和药物管道的结合已经允许开发各种酪氨酸激酶抑制剂,针对许多分子改变。这些药物现在可用于日常实践,并改变了EGFR、ALK或ROS1改变患者的生存结果。目前正在进行多项临床试验,以增加批准的药物数量,从而克服罕见突变和酪氨酸激酶抑制剂耐药性的问题。免疫检查点抑制剂的发展也改变了肺癌的预后,但反应率不高突出了对免疫生物标志物的需求。虽然PD-L1表达是第一个被批准的免疫生物标志物,但它已经显示出一些局限性,必须鉴定新的生物标志物来预测对免疫检查点抑制剂的反应或耐药性。在专门的分子多学科委员会的帮助下,测试方法、分子结果和靶向治疗计划将在未来几年协调一致。
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