Thoracic Oncology Program, Moffitt Cancer Center, Tampa, FL 33612, USA.
Cancer Control. 2014 Jan;21(1):67-73. doi: 10.1177/107327481402100110.
Lung cancer is the leading cause of cancer mortality. Non-small-cell lung cancer (NSCLC) comprises up to 90% of all lung cancers. Conventional treatment for advanced NSCLC consists of chemotherapy and has a small impact on survival. Molecular targets, such as epidermal growth factor receptor (EGFR), involved in cell signaling have led to the development of new, targeted therapies over the past 15 years.
Using a case report from our clinical practice, we review the literature and provide guidelines to the approach and management of advanced EGFR mutation-positive NSCLC.
Targeted and/or biologic (small molecules or monoclonal antibodies) cancer therapies have vaulted to the forefront of clinical research and therapeutic use. Our recommendation, backed by strong scientific evidence, is to treat patients with advanced or recurrent NSCLC harboring activating EGFR mutation with an EGFR tyrosine kinase inhibitor (TKI) as early as possible. Erlotinib is currently the drug of choice in the United States, although afatinib, due to its recent approval by the US Food and Drug Administration, will soon be available.
Improved understanding of cell signaling pathways that control cellular proliferation, differentiation, and survival combined with our increased ability to screen for specific mutations that drive malignant transformation and oncogenic behavior, has altered our treatment of advanced NSCLC. We can now provide a more individualized approach associated with improved progression-free survival and quality of life.
肺癌是癌症死亡的主要原因。非小细胞肺癌(NSCLC)占所有肺癌的 90%。晚期 NSCLC 的常规治疗包括化疗,但对生存的影响很小。细胞信号转导中涉及的分子靶点,如表皮生长因子受体(EGFR),导致了过去 15 年来新的靶向治疗方法的发展。
我们通过临床实践中的一个病例报告,回顾文献并提供了针对晚期 EGFR 突变阳性 NSCLC 的方法和管理的指南。
针对和/或生物(小分子或单克隆抗体)癌症疗法已成为临床研究和治疗应用的前沿。我们强烈推荐,具有激活 EGFR 突变的晚期或复发性 NSCLC 患者尽早使用 EGFR 酪氨酸激酶抑制剂(TKI)进行治疗。厄洛替尼目前是美国的首选药物,尽管 afatinib 最近获得了美国食品和药物管理局的批准,很快就会上市。
对控制细胞增殖、分化和存活的细胞信号通路的理解的提高,加上我们筛查驱动恶性转化和致癌行为的特定突变的能力的提高,改变了我们对晚期 NSCLC 的治疗方法。我们现在可以提供更个体化的治疗方法,从而提高无进展生存期和生活质量。