国际肿瘤学杂志 ›› 2024, Vol. 51 ›› Issue (2): 95-98.doi: 10.3760/cma.j.cn371439-20231008-00013

• 综述 • 上一篇    下一篇

非小细胞肺癌KRASG12C突变的研究进展

马正红1, 姜超2()   

  1. 1山东第一医科大学第三附属医院放疗科,济南 250031
    2山东第一医科大学第三附属医院肿瘤内科,济南 250031
  • 收稿日期:2023-10-08 修回日期:2023-11-04 出版日期:2024-02-08 发布日期:2024-04-03
  • 通讯作者: 姜超,Email:cyltjc1236@126.com

Progress of KRASG12C mutations in non-small cell lung cancer

Ma Zhenghong1, Jiang Chao2()   

  1. 1Department of Radiation Oncology,Third Affiliated Hospital of Shandong First Medical University,Jinan 250031,China
    2Department of Oncology,Third Affiliated Hospital of Shandong First Medical University,Jinan 250031,China
  • Received:2023-10-08 Revised:2023-11-04 Online:2024-02-08 Published:2024-04-03
  • Contact: Jiang Chao,Email:cyltjc1236@126.com

摘要:

随着KRASG12C突变在非小细胞肺癌靶向治疗中作用机制的不断深入研究,KRASG12C由“不可成药”发展为重要的靶向治疗位点。KRASG12C突变抑制剂在非小细胞肺癌靶向治疗中实现了有效率和生存的双进展。尽管治疗产生的耐药不可避免,但通过其耐药机制的研究发现,联合用药是克服或减少耐药的途径之一。

关键词: KRAS, 癌, 非小细胞肺, 分子靶向治疗

Abstract:

With the continuous in-depth research on the mechanism of KRASG12C mutations in targeted therapy of non-small cell lung cancer,KRASG12C has evolved from non producible to an important targeted therapy site. The KRASG12C mutation inhibitor has achieved dual progress in efficiency and survival in targeted therapy of non-small cell lung cancer. Although drug resistance is inevitable with treatment,research on drug resistance mechanisms has found that combination medication is one of the ways to overcome or reduce drug resistance.

Key words: KRAS, Carcinoma, non-small-cell lung, Molecular targeted therapies