Zheng Xinting, Luo Jiamin, Liu Wei, Ashby Charles R, Chen Zhe-Sheng, Lin Lizhu
Cancer Center, The First Affiliated Hospital to Guangzhou University of Chinese Medicine, Guangzhou, China.
The First Clinical Medical School of Guangzhou University of Chinese Medicine, Guangzhou, China.
Drugs Today (Barc). 2022 Apr;58(4):175-185. doi: 10.1358/dot.2022.58.4.3400573.
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.
索托拉西布是一种对携带G12C突变的 Kirsten 大鼠肉瘤病毒癌基因(KRAS)具有直接抑制作用的药物,基于一项II期临床试验(Code-BreaK100)的结果,它被美国食品药品监督管理局(FDA)批准作为二线治疗药物,用于治疗携带KRAS G12C突变的局部晚期或转移性非小细胞肺癌(NSCLC)。在本文中,我们回顾了KRAS G12C抑制剂的作用机制以及索托拉西布的最新临床试验情况,以便全面了解其疗效和毒性。我们还回顾了对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对携带KRAS G12C突变的NSCLC患者具有显著疗效且毒性可耐受,它可能代表一种新型靶向治疗方法。还需要进一步研究来阐明对索托拉西布产生耐药性的机制,并确定联合治疗对携带KRAS G12C突变的NSCLC的疗效和安全性。