First Clinical Medical College, Guangzhou University of Traditional Chinese, Guangzhou, China.
Department of Oncology, The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, Guangzhou, China.
Front Immunol. 2023 Jan 10;13:1088683. doi: 10.3389/fimmu.2022.1088683. eCollection 2022.
Genetic mutations that render mismatch repair defective may result in microsatellite instability, which is common in colorectal carcinomas and gastric cancers as well as Lynch syndrome. Mismatch repair deficiency/high microsatellite instability (dMMR/MSI-H) predicts the tumor response to immune checkpoint inhibitors. However, few studies have evaluated the efficacy of immune checkpoint inhibitors in non-small cell lung cancer (NSCLC) patients with dMMR/MSI-H. In this work, we present a patient with advanced squamous lung cancer with dMMR/MSI-H and a high tumor mutational burden (TMB-H) who obtained a long-term benefit from immunotherapy. NSCLC patients with dMMR/MSI-H/TMB-H may thus benefit from immune checkpoint inhibitors.
导致错配修复缺陷的基因突变可能导致微卫星不稳定,这在结直肠癌和胃癌以及林奇综合征中很常见。错配修复缺陷/高微卫星不稳定性(dMMR/MSI-H)预测肿瘤对免疫检查点抑制剂的反应。然而,很少有研究评估免疫检查点抑制剂在 dMMR/MSI-H 的非小细胞肺癌(NSCLC)患者中的疗效。在这项工作中,我们展示了一名患有晚期鳞状肺癌的患者,其错配修复缺陷/微卫星不稳定(dMMR/MSI-H)且肿瘤突变负担高(TMB-H),他从免疫治疗中获得了长期获益。因此,dMMR/MSI-H/TMB-H 的 NSCLC 患者可能受益于免疫检查点抑制剂。