Division of Medical Oncology, The Ottawa Hospital Cancer Center, Ottawa, Ontario, Canada.
Clin Lung Cancer. 2012 Jul;13(4):267-79. doi: 10.1016/j.cllc.2011.09.001. Epub 2011 Dec 9.
The epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) gefitinib and erlotinib have provided substantial benefits to patients with advanced non-small cell lung cancer (NSCLC). However resistance to these agents has emerged as a significant clinical issue; most patients who initially respond to treatment eventually experience relapse. The mechanisms underlying gefitinib and erlotinib resistance are multifactorial and several have been described. Clearly there is a need for novel and more effective therapies that can overcome resistance to the currently available TKIs. Several agents are in clinical development, including irreversible EGFR TKIs, inhibitors of the MET pathway, and others. In this review we discuss the various underlying mechanisms of gefitinib and erlotinib resistance and highlight the agents currently in clinical development that may have potential for overcoming this resistance.
表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)吉非替尼和厄洛替尼为晚期非小细胞肺癌(NSCLC)患者带来了显著的获益。然而,这些药物的耐药性已成为一个重要的临床问题;大多数最初对治疗有反应的患者最终会复发。吉非替尼和厄洛替尼耐药的机制是多因素的,已经有几种机制被描述。显然,需要新的、更有效的治疗方法来克服目前可用 TKI 的耐药性。有几种药物正在临床开发中,包括不可逆的 EGFR TKI、MET 通路抑制剂等。在这篇综述中,我们讨论了吉非替尼和厄洛替尼耐药的各种潜在机制,并强调了目前正在临床开发中可能具有克服这种耐药性潜力的药物。