Bouchard Nicole, Daaboul Nathalie
Centre Hospitalier Universitaire de Sherbrooke, Université de Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.
Centre Intégré de Cancérologie de la Montérégie, Université de Sherbrooke, Longueuil, QC J4V 2H1, Canada.
Curr Oncol. 2025 Mar 2;32(3):146. doi: 10.3390/curroncol32030146.
Lung cancer treatment has changed in the last twenty years since the discovery of EGFR mutations. In this article, we will review the current state of the art for non-small cell lung cancer (NSCLC) actionable genomic alterations (AGA). AGAs are mostly found in lung adenocarcinomas, a subtype of non-small cell lung cancers. We will focus on the current treatment for EGFR mutations, ALK fusions, ROS1 fusions, BRAF V600E mutations, MET exon 14-skipping mutations, RET fusions, KRAS G12C mutations, ERBB2 mutations (also called HER2 mutations), and NTRK fusions. We will also touch on the key toxicities associated with these medications. Treatments are mostly available for the metastatic stage, but we will also discuss adjuvant therapy for EGFR mutations and ALK fusions, as well as stage III post-chemoradiotherapy treatment for EGFR lung cancer.
自发现EGFR突变以来的过去二十年里,肺癌治疗发生了变化。在本文中,我们将回顾非小细胞肺癌(NSCLC)可操作基因组改变(AGA)的当前技术水平。AGA大多见于肺腺癌,这是一种非小细胞肺癌的亚型。我们将重点关注EGFR突变、ALK融合、ROS1融合、BRAF V600E突变、MET外显子14跳跃突变、RET融合、KRAS G12C突变、ERBB2突变(也称为HER2突变)和NTRK融合的当前治疗方法。我们还将提及与这些药物相关的关键毒性。治疗方法大多适用于转移阶段,但我们也将讨论EGFR突变和ALK融合的辅助治疗,以及EGFR肺癌的III期放化疗后治疗。