Resistance to KRAS inhibition in advanced non-small cell lung cancer

K. Sreter, Maria Joana Pereira Catarata, Maximilian von Laffert, Armin Frille
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Abstract

Lung cancer remains the leading cause of cancer death globally. More than 50% of new cases are diagnosed in an advanced or metastatic stage, thus contributing to the poor survival of such patients. Mutations in the KRAS (Kirsten rat sarcoma virus) gene occur in nearly a third of lung adenocarcinoma and have for decades been deemed an ‘undruggable’ target. Yet, in recent years, a growing number of small molecules, such as the GTPase inhibitors, has been investigated in clinical trials of lung cancer patients harboring KRAS mutations, yielding promising results with improved outcomes. Currently, there are only two approved targeted therapies (adagrasib and sotorasib) for advanced or metastatic KRAS-mutated NSCLC from the second-line setting onwards. In this narrative review, we will focus on KRAS, its molecular basis, the role of its co-mutations, clinical evidence for its inhibition, putative mutation to resistance, and future strategies to overcome resistance to KRAS inhibition.
晚期非小细胞肺癌患者对 KRAS 抑制剂的抗药性
肺癌仍然是全球癌症死亡的主要原因。50%以上的新病例确诊时已是晚期或转移期,因此这类患者的生存率很低。近三分之一的肺腺癌发生 KRAS(克氏大鼠肉瘤病毒)基因突变,几十年来一直被认为是 "不可药治 "的靶点。然而,近年来,越来越多的小分子药物(如 GTPase 抑制剂)已在携带 KRAS 基因突变的肺癌患者的临床试验中进行了研究,并取得了改善预后的良好结果。目前,只有两种获批的靶向疗法(adagrasib 和 sotorasib)可用于晚期或转移性 KRAS 突变 NSCLC 的二线治疗。在这篇叙述性综述中,我们将重点介绍 KRAS、其分子基础、共突变的作用、抑制 KRAS 的临床证据、假定突变导致的耐药性以及克服 KRAS 抑制耐药性的未来策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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