Nguyen Kim-Son H, Neal Joel W, Wakelee Heather
Kim-Son H Nguyen, Joel W Neal, Heather Wakelee, Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, United States.
World J Clin Oncol. 2014 Oct 10;5(4):576-87. doi: 10.5306/wjco.v5.i4.576.
The last decade has witnessed the development of oncogene-directed targeted therapies that have significantly changed the treatment of non-small-cell lung cancer (NSCLC). In this paper we review the data demonstrating efficacy of gefitinib, erlotinib, and afatinib, which target the epidermal growth factor receptor (EGFR), and crizotinib which targets anaplastic lymphoma kinase (ALK). We discuss the challenge of acquired resistance to these small-molecular tyrosine kinase inhibitors and review promising agents which may overcome resistance, including the EGFR T790M-targeted agents CO-1686 and AZD9291, and the ALK-targeted agents ceritinib (LDK378), AP26113, alectinib (CH/RO5424802), and others. Emerging therapies directed against other driver oncogenes in NSCLC including ROS1, HER2, and BRAF are covered as well. The identification of specific molecular targets in a significant fraction of NSCLC has led to the personalized deployment of many effective targeted therapies, with more to come.
过去十年见证了癌基因导向的靶向治疗的发展,这些治疗显著改变了非小细胞肺癌(NSCLC)的治疗方式。在本文中,我们回顾了证明吉非替尼、厄洛替尼和阿法替尼(它们靶向表皮生长因子受体(EGFR))以及克唑替尼(靶向间变性淋巴瘤激酶(ALK))疗效的数据。我们讨论了对这些小分子酪氨酸激酶抑制剂产生获得性耐药的挑战,并回顾了可能克服耐药性的有前景的药物,包括EGFR T790M靶向药物CO-1686和AZD9291,以及ALK靶向药物色瑞替尼(LDK378)、AP26113、阿来替尼(CH/RO5424802)等。还涵盖了针对NSCLC中其他驱动癌基因(包括ROS1, HER2和BRAF)的新兴疗法。在很大一部分NSCLC中鉴定出特定分子靶点,已导致许多有效靶向治疗的个性化应用,且更多的靶向治疗即将出现。