Sotorasib: a treatment for non-small cell lung cancer with the KRAS G12C mutation.

Xinting Zheng, Jiamin Luo, Wei Liu, C. Ashby, Zhe S Chen, Lizhu Lin
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引用次数: 4

Abstract

Sotorasib, a direct inhibitor of the enzyme Kirsten rat sarcoma viral oncogene (KRAS) with the G12C mutation, was approved by the U.S. Food and Drug Administration (FDA), as a second-line treatment for locally advanced or metastatic non-small cell lung cancer (NSCLC) containing the KRAS G12C mutation, on the basis of results of a phase II clinical trial (Code- BreaK100). In this article, we review the mechanism of action of KRAS G12C inhibitors and the latest clinical trials with sotorasib to provide a comprehensive understanding of its efficacy and toxicity. We also review the mechanisms that produce resistance to the KRAS G12C inhibitors and the preclinical research related to combination treatments for KRAS G12C-mutated tumors. Currently, clinical data suggests that sotorasib monotherapy has significant efficacy in NSCLC patients with the KRAS G12C mutation and tolerable toxicity, and it could represent a novel targeted therapy. Additional research will be required to delineate the mechanisms of resistance to sotorasib and determine the efficacy and safety of combination therapy for the treatment of NSCLC containing the KRAS G12C mutation.
索托拉西布:治疗KRAS G12C突变的癌症。
根据II期临床试验(Code-BreaK100)的结果,Sotorasib是一种具有G12C突变的Kirsten大鼠肉瘤病毒癌基因(KRAS)酶的直接抑制剂,被美国食品药品监督管理局(FDA)批准为含有KRAS G12C突变局部晚期或转移性非小细胞肺癌(NSCLC)的二线治疗药物。在这篇文章中,我们回顾了KRAS G12C抑制剂的作用机制和索托拉西布的最新临床试验,以全面了解其疗效和毒性。我们还综述了对KRAS G12C抑制剂产生耐药性的机制,以及与KRAS G12C-突变肿瘤联合治疗相关的临床前研究。目前,临床数据表明,索托拉西布单药治疗KRAS G12C突变和可耐受毒性的NSCLC患者具有显著疗效,可能是一种新的靶向治疗方法。还需要进一步的研究来描述对索托拉西布的耐药性机制,并确定联合治疗含有KRAS G12C突变的NSCLC的疗效和安全性。
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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