Department of Oncology, University of Turin, S. Luigi Gonzaga Hospital, Orbassano (TO), Italy.
Department of Public Health, University of Naples Federico II, Naples, Italy.
Eur J Cancer. 2020 Sep;137:57-68. doi: 10.1016/j.ejca.2020.06.023. Epub 2020 Jul 31.
Despite the high prevalence of Kirsten rat sarcoma (KRAS) mutations in non-small cell lung cancer (NSCLC), for a long time it has been defined as an 'undruggable target', with precision medicine not considered as an adequate approach to treat this subgroup of patients. After several years of efforts, preliminary data from early clinical trials have recently demonstrated that direct pharmacological inhibition of KRAS p.G12C mutation is possible, emerging as an effective targeted treatment for about 10-12% of patients with advanced NSCLC, with potential relevant impact on their long-term survival and quality of life. This review reports the current status of KRAS mutations detection in the Italian real-word scenario, summarises the biological basis of KRAS inhibition in NSCLC and provides an updated overview of therapeutic strategies, discussing the potential reasons for past failures and analysing the upcoming challenges related to the advent of new targeted agents in clinical practice.
尽管 Kirsten 大鼠肉瘤 (KRAS) 突变在非小细胞肺癌 (NSCLC) 中的患病率很高,但长期以来,它一直被定义为一个“不可成药的靶点”,精准医学也不被认为是治疗这组患者的合适方法。经过多年的努力,最近早期临床试验的初步数据表明,直接抑制 KRAS p.G12C 突变是可能的,这为大约 10-12%的晚期 NSCLC 患者提供了一种有效的靶向治疗方法,可能对他们的长期生存和生活质量产生重要影响。这篇综述报告了 KRAS 突变在意大利真实世界背景下的检测现状,总结了 KRAS 抑制在 NSCLC 中的生物学基础,并提供了治疗策略的最新概述,讨论了过去失败的潜在原因,并分析了与新的靶向药物在临床实践中应用相关的未来挑战。