Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California.
Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California; Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
J Thorac Oncol. 2021 Mar;16(3):395-403. doi: 10.1016/j.jtho.2020.11.015. Epub 2020 Dec 8.
The KEAP1-NFE2L2 pathway is an important modulator of cell homeostasis. Mutations in this pathway are common in NSCLC and have been associated with enhanced tumor growth and aggressiveness. In addition, tumors with mutations in the KEAP1-NFE2L2 pathway have been reported in preclinical and clinical studies to convey refractoriness to cancer-directed therapy such as radiation, chemotherapy, and targeted therapy. The role of immunotherapy in this patient population is less clear, and there are conflicting studies on the efficacy of immune checkpoint inhibitors in KEAP1-NFE2L2-mutant NSCLC. Here, we review the current clinical evidence on several classes of anticancer therapeutics in KEAP1-NFE2L2-mutant tumors. Furthermore, we provide an overview of the landscape of the current clinical trials in this patient population, highlighting the work being done with mTORC1, mTORC2, and glutaminase inhibition.
KEAP1-NFE2L2 通路是细胞内稳态的重要调节因子。该通路中的突变在 NSCLC 中很常见,并与增强的肿瘤生长和侵袭性有关。此外,在临床前和临床研究中,已经报道了具有 KEAP1-NFE2L2 通路突变的肿瘤对癌症定向治疗(如放疗、化疗和靶向治疗)产生耐药性。免疫疗法在这一患者人群中的作用尚不清楚,并且在免疫检查点抑制剂在 KEAP1-NFE2L2 突变型 NSCLC 中的疗效方面存在相互矛盾的研究。在这里,我们回顾了 KEAP1-NFE2L2 突变型肿瘤中几种抗癌治疗药物的临床证据。此外,我们概述了该患者人群中目前临床试验的概况,重点介绍了正在进行的 mTORC1、mTORC2 和谷氨酰胺酶抑制的研究工作。