Zhang Shannon S, Lee Alexandria, Nagasaka Misako
University of California Irvine School of Medicine, Orange, CA, USA.
St. Marianna University School of Medicine, Kawasaki, Japan.
Lung Cancer (Auckl). 2023 Apr 19;14:27-30. doi: 10.2147/LCTT.S403461. eCollection 2023.
Thirteen percent of non-small cell lung cancer (NSCLC) patients are estimated to have the KRAS G12C mutation. Sotorasib is a novel KRAS G12C inhibitor that has shown promising results in preclinical and clinical studies, granting its conditional approval by the FDA in May 2021. The phase I clinical trial resulted in a confirmed response of 32% and progression free survival (PFS) of 6.3 months while the phase II trial resulted in a confirmed response of 37.1% and a PFS of 6.8 months. It was also shown to be tolerable with most subjects experiencing grade one or two adverse events, most commonly diarrhea and nausea. The CodeBreaK 200 phase III trial data have recently resulted and showed an improved PFS with the use of sotorasib at 5.6 months compared to that of standard docetaxel of 4.5 months in locally advanced or unresectable metastatic KRAS G12C NSCLC previously treated with at least one platinum-based chemotherapy and checkpoint inhibitor. The lower than expected PFS of sotorasib from the phase III trial opens up opportunities for other G12C inhibitors to join the field. Indeed, adagrasib, another G12C inhibitor just recently gained FDA accelerated approval in NSCLC patients based on the KRYSTAL-1 study where the response rate was 43% with a median duration of response of 8.5 months. With novel agents and combinations, the field of KRAS G12C is quickly evolving. While sotorasib was an exciting start, there is more to do to break the KRAS G12C Enigma code.
据估计,13%的非小细胞肺癌(NSCLC)患者存在KRAS G12C突变。索托拉西布是一种新型的KRAS G12C抑制剂,在临床前和临床研究中均显示出有前景的结果,并于2021年5月获得了美国食品药品监督管理局(FDA)的有条件批准。I期临床试验的确认缓解率为32%,无进展生存期(PFS)为6.3个月,而II期临床试验的确认缓解率为37.1%,PFS为6.8个月。研究还表明,大多数受试者对其耐受性良好,最常见的不良事件为1级或2级,主要是腹泻和恶心。CodeBreaK 200 III期试验的数据最近公布,结果显示,在先前接受过至少一种铂类化疗和检查点抑制剂治疗的局部晚期或不可切除的转移性KRAS G12C NSCLC患者中,使用索托拉西布的PFS有所改善,为5.6个月,而标准多西他赛的PFS为4.5个月。III期试验中索托拉西布的PFS低于预期,这为其他G12C抑制剂进入该领域创造了机会。事实上,另一种G12C抑制剂阿达格拉西布最近基于KRYSTAL-1研究获得了FDA对NSCLC患者的加速批准,该研究的缓解率为43%,中位缓解持续时间为8.5个月。随着新型药物和联合治疗方案的出现,KRAS G12C领域正在迅速发展。虽然索托拉西布是一个令人兴奋的开端,但要破解KRAS G12C之谜,还有更多工作要做。