Higgins Jordyn P, Carlisle Jennifer W, Moniri Nader H, Gupta Shruti, Oduah Eziafa I, Leal Ticiana
Department of Pharmacy, Duke University Hospital, Durham, NC, USA.
Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
Future Oncol. 2025 Jan;21(1):63-71. doi: 10.1080/14796694.2024.2430172. Epub 2024 Nov 27.
Kirsten rat sarcoma viral oncogene homolog (KRAS) mutation is prognostic of poor survival for patients with non-small cell lung cancer (NSCLC). KRAS G12C mutations occur in 13% of NSCLC cases and despite the frequency of this mutation, advances in drug development against KRAS have historically been impeded due to the extremely high affinity of KRAS for guanosine triphosphate (GTP) and the lack of a binding pocket on the surface of KRAS that is suitable for drug binding. Sotorasib, a first-in-class, highly selective KRAS G12C inhibitor overcomes this issue by irreversibly binding in the switch-II pocket. Sotorasib was granted accelerated FDA approval for the treatment of KRASG12C-mutated locally advanced/metastatic NSCLC who have received at least one prior systemic therapy. This review summarizes the pharmacology, clinical efficacy, adverse effects, and clinical considerations of sotorasib.
Kirsten 大鼠肉瘤病毒癌基因同源物(KRAS)突变预示着非小细胞肺癌(NSCLC)患者的生存率较低。KRAS G12C 突变发生在 13%的 NSCLC 病例中,尽管该突变频率较高,但由于 KRAS 对三磷酸鸟苷(GTP)具有极高的亲和力,且 KRAS 表面缺乏适合药物结合的结合口袋,因此针对 KRAS 的药物开发进展一直受到阻碍。索托拉西布是首个同类高度选择性的 KRAS G12C 抑制剂,它通过不可逆地结合在开关-II 口袋中来克服这一问题。索托拉西布已获得美国食品药品监督管理局(FDA)的加速批准,用于治疗接受过至少一种先前全身治疗的 KRASG12C 突变的局部晚期/转移性 NSCLC。本综述总结了索托拉西布的药理学、临床疗效、不良反应及临床注意事项。