Thoracic and Gastrointestinal Oncology Branch, Center for Cancer Research, Building 10, 4-4553, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-1201, USA.
Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, 3970 Reservoir Road North West, Washington, DC 20057, USA.
Nat Rev Clin Oncol. 2015 Sep;12(9):511-26. doi: 10.1038/nrclinonc.2015.90. Epub 2015 May 12.
In the past decade, the characterization of non-small-cell lung cancer (NSCLC) into subtypes based on genotype and histology has resulted in dramatic improvements in disease outcome in select patient subgroups. In particular, molecularly targeted agents that inhibit EGFR or ALK are approved for the treatment of NSCLC harbouring genetic alterations in the genes encoding these proteins. Although acquired resistance usually limits the duration of response to these therapies, a number of new agents have proven effective at tackling specific resistance mechanisms to first-generation inhibitors. Large initiatives are starting to address the role of biomarker-driven targeted therapy in squamous lung cancers, and in the adjuvant setting. Immunotherapy undeniably holds great promise and our understanding of subsets of NSCLC based on patterns of immune response is continuing to evolve. In addition, efforts are underway to identify rare genomic subsets through genomic screening, functional studies, and molecular characterization of exceptional responders. This Review provides an overview of the key developments in the treatment of NSCLC, and discusses potential strategies to further optimize therapy by targeting disease subtypes.
在过去的十年中,根据基因型和组织学将非小细胞肺癌(NSCLC)分为亚型,这使得某些患者亚组的疾病预后得到了显著改善。特别是,针对这些蛋白编码基因中存在遗传改变的 NSCLC,抑制 EGFR 或 ALK 的分子靶向药物已被批准用于治疗。尽管获得性耐药通常限制了这些治疗的反应持续时间,但许多新药物已被证明可有效解决第一代抑制剂的特定耐药机制。大型计划开始解决生物标志物驱动的靶向治疗在鳞状肺癌中的作用,以及辅助治疗中的作用。免疫疗法无疑具有巨大的潜力,我们对基于免疫反应模式的 NSCLC 亚组的理解也在不断发展。此外,正在通过基因组筛选、功能研究和对异常反应者的分子特征进行研究,努力识别罕见的基因组亚组。本综述概述了 NSCLC 治疗方面的重要进展,并讨论了通过针对疾病亚型进一步优化治疗的潜在策略。