Challenge and countermeasures for EGFR targeted therapy in non-small cell lung cancer

肺癌 靶向治疗 表皮生长因子受体 医学 PI3K/AKT/mTOR通路 癌症 癌症研究 临床试验 酪氨酸激酶 肿瘤科 精密医学 肺癌的治疗 生物信息学 内科学 生物 信号转导 病理 受体 生物化学
作者
Xueli Tian,Tingxuan Gu,Mee‐Hyun Lee,Zigang Dong
出处
期刊:Biochimica Et Biophysica Acta - Reviews On Cancer [Elsevier BV]
卷期号:1877 (1): 188645-188645 被引量:82
标识
DOI:10.1016/j.bbcan.2021.188645
摘要

Lung cancer causes the highest mortality compared to other cancers in the world according to the latest WHO reports. Non-small cell lung cancer (NSCLC) contributes about 85% of total lung cancer cases. An extensive number of risk factors are attributed to the progression of lung cancer. Epidermal growth factor receptor (EGFR), one of the most frequently mutant driver genes, is closely involved in the development of lung cancer through regulation of the PI3K/AKT and MAPK pathways. As a representative of precision medicine, EGFR-tyrosine kinase inhibitors (TKIs) targeted therapy significantly relieves the development of activating mutant EGFR-driven NSCLC. However, treatment with TKIs facilitates the emergence of acquired resistance that continues to pose a significant hurdle with respect to EGFR targeted therapy. In this review, the development of current approved EGFR-TKIs as well as the related supporting clinical trials are summarized and discussed. Mechanisms of action and resistance were addressed respectively, which serve as important guides to understanding acquired resistance. We also explored the corresponding combination treatment options according to different resistance mechanisms. Future challenges include more comprehensive characterization of unclear resistance mechanisms in different populations and the development of more efficient and precision synthetic therapeutic strategies.
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