Formisano Luigi, Jansen Valerie M, Marciano Roberta, Bianco Roberto
Department of Clinical Medicine and Surgery, University Federico II of Naples, Italy.
Department of Medicine, Division of Hematology-Oncology, Vanderbilt University Medical Center, Nashville, Tennessee, United States.
Anticancer Agents Med Chem. 2018;18(9):1235-1240. doi: 10.2174/1871520617666170912123416.
Lung cancer is the leading cause of cancer-related mortality around the world, despite effective chemotherapeutic agents, the prognosis has remained poor for a long time. The discovery of molecular changes that drive lung cancer has led to a dramatic shift in the therapeutic landscape of this disease. In "in vitro" and "in vivo" models of NSCLC (Non-Small Cell Lung Cancer), angiogenesis blockade has demonstrated an excellent anti-tumor activity, thus, a number of anti-angiogenic drugs have been approved by regulatory authorities for use in clinical practice. Much more interesting is the discovery of EGFR (Epithelial Growth Factor Receptor) mutations that predict sensitivity to the anti-EGFR Tyrosine Kinase Inhibitors (TKIs), a class of drugs that has shown to significantly improve survival when compared with standard chemotherapy in the first-line treatment of metastatic NSCLC. Nevertheless, after an initial response, resistance often occurs and prognosis becomes dismal. Biomolecular studies on cell line models have led to the discovery of mutations (e.g., T790M) that confer resistance to anti-EGFR inhibitors. Fortunately, drugs that are able to circumvent this mechanism of resistance have been developed and have been recently approved for clinical use. The discovery of robust intratumor lymphocyte infiltration in NSCLC has paved the way to several strategies able to restore the immune response. Thus, agents interfering with PD-1/PD-L1 (Programmed Death) pathways make up a significant portion of the armamentarium of cancer therapies for NSCLC. In all the above-mentioned situations, the basis of the success in treating NSCLC has started from understanding of the mutational landscape of the tumor.
肺癌是全球癌症相关死亡的主要原因,尽管有有效的化疗药物,但长期以来预后仍然很差。驱动肺癌的分子变化的发现导致了该疾病治疗格局的巨大转变。在非小细胞肺癌(NSCLC)的“体外”和“体内”模型中,血管生成阻断已显示出出色的抗肿瘤活性,因此,一些抗血管生成药物已获得监管机构批准用于临床实践。更有趣的是表皮生长因子受体(EGFR)突变的发现,这些突变可预测对抗EGFR酪氨酸激酶抑制剂(TKIs)的敏感性,与转移性NSCLC一线治疗中的标准化疗相比,这类药物已显示出可显著提高生存率。然而,在初始反应后,耐药性经常出现,预后变得很差。对细胞系模型的生物分子研究导致了赋予抗EGFR抑制剂耐药性的突变(例如T790M)的发现。幸运的是,能够规避这种耐药机制的药物已经开发出来,并且最近已被批准用于临床。NSCLC中强大的肿瘤内淋巴细胞浸润的发现为几种能够恢复免疫反应的策略铺平了道路。因此,干扰程序性死亡蛋白1(PD-1)/程序性死亡配体1(PD-L1)途径的药物构成了NSCLC癌症治疗手段的重要组成部分。在上述所有情况下,治疗NSCLC成功的基础始于对肿瘤突变格局的了解。