国际肿瘤学杂志 ›› 2021, Vol. 48 ›› Issue (11): 683-687.doi: 10.3760/cma.j.cn371439-20201231-00135

• 综述 • 上一篇    下一篇

免疫检查点抑制剂在肺癌治疗中的研究进展

马骏1, 张红颖1, 吴艾平1, 高广毅2()   

  1. 1南京中医药大学附属淮安中医院肿瘤科,淮安 223001
    2江苏省淮安市第二人民医院肿瘤科 223001
  • 收稿日期:2020-12-31 修回日期:2021-04-30 出版日期:2021-11-08 发布日期:2021-12-14
  • 通讯作者: 高广毅 E-mail:516048620@qq.com
  • 基金资助:
    江苏省中医药科技发展计划(YB201967)

Research progress of immune checkpoint inhibitors in the treatment of lung cancer

Ma Jun1, Zhang Hongying1, Wu Aiping1, Gao Guangyi2()   

  1. 1Department of Oncology, Huai'an Traditional Chinese Medicine Hospital Affiliated to Nanjing University of Chinese Medicine, Huai'an 223001, China
    2Department of Oncology, Huai'an Second People's Hospital of Jiangsu Province, Huai'an 223001, China
  • Received:2020-12-31 Revised:2021-04-30 Online:2021-11-08 Published:2021-12-14
  • Contact: Gao Guangyi E-mail:516048620@qq.com
  • Supported by:
    Science and Technology Development Plan of Traditional Chinese Medicine of Jiangsu Province of China(YB201967)

摘要:

近年来,免疫检查点抑制剂在肺癌的治疗中是一个里程碑式的突破。免疫检查点种类较多,包括程序性死亡蛋白-1(PD-1)、程序性死亡蛋白配体-1(PD-L1)、细胞毒性T淋巴细胞抗原4(CTLA-4)、杀伤细胞免疫球蛋白样受体(KIR)、T细胞免疫球蛋白和ITIM结构域蛋白(TIGIT)、细胞免疫球蛋白和黏蛋白3(TIM-3)等,与免疫治疗的疗效及耐药密切相关。PD-1/PD-L1抑制剂已被中国国家药品监督管理局及美国食品药品监督管理局批准用于肺癌的一线治疗,可延长患者的总生存期及无进展生存期。CTLA-4抑制剂或TIGIT抑制剂联合PD-1/PD-L1抑制剂的双免疫治疗亦取得良好疗效,但可能发生更严重的不良事件。KIR及TIM-3靶点与免疫治疗的耐药性密切相关。

关键词: 免疫疗法, 肺肿瘤, 免疫检查点抑制剂

Abstract:

In recent years, immune checkpoint inhibitors are a milestone in the treatment of lung cancer. There are many kinds of immune checkpoints, which are closely related to the efficacy and drug resis-tance of immunotherapy, including programmed death-1 (PD-1), programmed death ligand-1 (PD-L1), cytotoxic T-lymphocyte antigen 4 (CTLA-4), killer cell immunoglobulin-like receptor (KIR), T cell immunoglobulin and ITIM domain (TIGIT), T-cell immunoglobulin and mucin domain-containing protein 3 (TIM-3), etc. PD-1/PD-L1 inhibitors have been approved by China National Medical Products Administration and U.S. Food and Drug Administration for the first-line treatment of lung cancer, which can improve overall survival and progression-free survival of patients. The double immunotherapies of CTLA-4 inhibitors or TIGIT inhibitors combined with PD-1/PD-L1 inhibitors also achieve good results, however, more serious adverse events may occur.The KIR and TIM-3 targets are closely related to the drug resistance of immunotherapy.

Key words: Immunotherapy, Lung neoplasms, Immune checkpoint inhibitors