Deming Dustin A
1Division of Hematology, Medical Oncology, and Palliative Care, Department of Medicine, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI.
2University of Wisconsin Carbone Cancer Center, Madison, WI.
J Natl Compr Canc Netw. 2025 Jan 3;23(1):e247067. doi: 10.6004/jnccn.2024.7067.
Colorectal cancer (CRC) is a heterogeneous group of diseases comprising several molecular subtypes. Comprehensive DNA sequencing is now standard practice to identify these subtype. Until recently, KRAS mutation status in metastatic CRC was primarily used as a biomarker to predict resistance to EGFR inhibition. However, with up to 40% of CRC cases harboring KRAS mutations, therapeutic targeting of RAS has been an area of great need. The development of KRASG12C inhibitors has led to the FDA approval of drugs for treating non-small cell lung cancer. Recently, these and other newly developed inhibitors have been investigated as monotherapies and in combination for metastatic KRASG12C-mutant CRC. This review examines the development of these inhibitors and highlights data supporting the inclusion of sotorasib and adagrasib, in combination with either panitumumab or cetuximab, in the NCCN Guidelines for CRC for the treatment of refractory metastatic disease.
结直肠癌(CRC)是一组异质性疾病,包括几种分子亚型。全面的DNA测序现已成为识别这些亚型的标准做法。直到最近,转移性CRC中的KRAS突变状态主要用作预测对EGFR抑制耐药性的生物标志物。然而,由于高达40%的CRC病例携带KRAS突变,RAS的治疗靶向一直是一个迫切需要的领域。KRASG12C抑制剂的开发已导致FDA批准用于治疗非小细胞肺癌的药物。最近,这些以及其他新开发的抑制剂已作为单药疗法以及联合用于转移性KRASG12C突变型CRC进行了研究。本综述探讨了这些抑制剂的开发,并强调了支持将索托拉西布和阿达格拉西布与帕尼单抗或西妥昔单抗联合纳入NCCN结直肠癌指南以治疗难治性转移性疾病的数据。