Black Robert C, Khurshid Humera
Fellow in the Div. of Hematology/Oncology at the Alpert Medical School of Brown University.
Medical oncologist at the Comprehensive Cancer Center at Rhode Island Hospital and an Assistant Professor at The Warren Alpert Medical School of Brown University.
R I Med J (2013). 2015 Oct 1;98(10):25-8.
Lung cancer is the most common malignancy in the US and causes the most cancer-related deaths. Non-small-cell lung carcinoma (NSCLC) accounts for the majority of cases. NSCLC historically was considered one entity, reflected by platinum-based therapy as the standard of care; however, with the discovery of EGFR mutations and ALK rearrangements, the landscape of treatment has become more personalized reflecting genomic heterogeneity. The molecular basis for tumor genesis was recognized and became a new method of classification. The availability of tumor sequencing and testing for these mutations is also becoming more accessible outside of major academic institutions. Targeted therapies offer alternatives to dangerous cytotoxic chemotherapy with equal or better efficacy. With these changes, driver mutations will play an increasing role in the diagnosis and treatment of NSCLC. In this review we will examine the characteristics of several NSCLC driver mutations and gene rearrangements and emerging data on therapies directed against them.
肺癌是美国最常见的恶性肿瘤,也是导致癌症相关死亡最多的疾病。非小细胞肺癌(NSCLC)占大多数病例。历史上,NSCLC被视为一个整体,以铂类疗法作为标准治疗方法来体现;然而,随着表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)重排的发现,治疗格局已变得更加个性化,反映出基因组异质性。肿瘤发生的分子基础得到了认可,并成为一种新的分类方法。除了主要学术机构外,肿瘤测序和这些突变检测的可用性也越来越容易获得。靶向治疗提供了替代危险细胞毒性化疗的方法,且疗效相同或更好。随着这些变化,驱动突变将在NSCLC的诊断和治疗中发挥越来越重要的作用。在这篇综述中,我们将研究几种NSCLC驱动突变和基因重排的特征以及针对它们的疗法的新出现的数据。