KRAS inhibition in non-small cell lung cancer: Past failures, new findings and upcoming challenges

被引:33
|
作者
Passiglia, Francesco [1 ]
Malapelle, Umberto [2 ]
Del Re, Marzia [3 ]
Righi, Luisella [1 ]
Pagni, Fabio [4 ]
Furlan, Daniela [5 ]
Danesi, Romano [3 ]
Troncone, Giancarlo [2 ]
Novello, Silvia [1 ]
机构
[1] Univ Turin, S Luigi Gonzaga Hosp, Dept Oncol, Reg Gonzole 10, I-10034 Orbassano, TO, Italy
[2] Univ Naples Federico II, Dept Publ Hlth, Naples, Italy
[3] Univ Hosp Pisa, Dept Clin & Expt Med, Clin Pharmacol & Pharmacogenet Unit, Pisa, Italy
[4] Univ Milano Bicocca, San Gerardo Hosp, Dept Med & Surg, Pathol, I-20900 Monza, Italy
[5] Univ Insubria, Dept Med & Surg, Pathol Unit, I-21100 Varese, Italy
关键词
KRAS; Lung cancer; AMG510; G12C; Target therapy; RANDOMIZED PHASE-II; K-RAS; ONCOGENIC KRAS; TUMOR-GROWTH; ASSOCIATION; TRAMETINIB; PACLITAXEL; LONAFARNIB; RIBOZYME;
D O I
10.1016/j.ejca.2020.06.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 demon-strated 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 up-dated 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. (c) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:57 / 68
页数:12
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