Division of Medical Oncology, National Cancer Centre Singapore, Singapore.
Duke-NUS Medical School, National University of Singapore, Singapore.
J Clin Oncol. 2022 Feb 20;40(6):611-625. doi: 10.1200/JCO.21.01626. Epub 2022 Jan 5.
Lung cancer has traditionally been classified by histology. However, a greater understanding of disease biology and the identification of oncogenic driver alterations has dramatically altered the therapeutic landscape. Consequently, the new classification paradigm of non-small-cell lung cancer is further characterized by molecularly defined subsets actionable with targeted therapies and the treatment landscape is becoming increasingly complex. This review encompasses the current standards of care for targeted therapies in lung cancer with driver molecular alterations. Targeted therapies for exon 19 deletion and L858R mutations, and and rearrangements are well established. However, there is an expanding list of approved targeted therapies including for V600E, exon 20 insertion, and G12C mutations, exon 14 alterations, and and rearrangements. In addition, there are numerous other oncogenic drivers, such as exon 20 insertion mutations, for which there are emerging efficacy data for targeted therapies. The importance of diagnostic molecular testing, intracranial efficacy of novel therapies, the optimal sequencing of therapies, role for targeted therapies in early-stage disease, and future directions for precision oncology approaches to understand tumor evolution and therapeutic resistance are also discussed.
肺癌传统上通过组织学进行分类。然而,对疾病生物学的更深入了解以及致癌驱动因素改变的鉴定,极大地改变了治疗格局。因此,非小细胞肺癌的新分类模式进一步以可通过靶向治疗靶向的分子定义亚组为特征,并且治疗领域变得越来越复杂。这篇综述涵盖了具有驱动分子改变的肺癌靶向治疗的当前护理标准。针对外显子 19 缺失和 L858R 突变以及 和 重排的靶向治疗已经确立。然而,有越来越多的批准的靶向治疗方法,包括针对 V600E、外显子 20 插入和 G12C 突变、外显子 14 改变以及 和 重排。此外,还有许多其他致癌驱动因素,例如 外显子 20 插入突变,针对这些驱动因素有新兴的靶向治疗疗效数据。还讨论了诊断性分子检测的重要性、新型疗法在颅内的疗效、治疗方案的最佳顺序、靶向治疗在早期疾病中的作用以及肿瘤进化和治疗耐药性的精准肿瘤学方法的未来方向。