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PD-1/PD-L1抑制剂在晚期肝细胞肝癌治疗中的研究进展
引用本文:李洁琅,陈婷,杨雨. PD-1/PD-L1抑制剂在晚期肝细胞肝癌治疗中的研究进展[J]. 中国肿瘤临床, 2020, 47(5): 265-268. DOI: 10.3969/j.issn.1000-8179.2020.05.187
作者姓名:李洁琅  陈婷  杨雨
作者单位:四川大学华西医院腹部肿瘤科(成都市 610000)
摘    要:晚期原发性肝细胞肝癌(hepatocellular carcinoma,HCC)的系统治疗主要包括靶向治疗、化疗以及免疫治疗。近3年,程序性死亡受体-1(programmed death receptor-1,PD-1)/程序性死亡受体-1配体(programmed death receptor-1 ligand,PD-L1)抑制剂在晚期HCC治疗中取得突破性进展。纳武单抗(nivolumab)和帕博利珠单抗(pembrolizumab)先后被美国食品药品管理局(FDA)批准用于HCC二线治疗。多个PD-1/PD-L1抑制剂联合系统治疗的Ⅰ、Ⅱ期临床研究初步显示出较好的疗效和安全性。阿特珠单抗(atezolizumab)联合贝伐单抗一线治疗成为首个在Ⅲ期临床研究中证实优于现有标准治疗索拉非尼的全新疗法。本文就近年PD-1/PD-L1抑制剂在晚期HCC治疗中的研究进展进行概述。

关 键 词:肝细胞癌  免疫治疗  PD-1抑制剂  PD-L1抑制剂
收稿时间:2020-01-03

Research progress in the use of PD-1/PD-L1 inhibitors for advanced hepatocellular carcinoma
Jielang Li,Ting Chen,Yu Yang. Research progress in the use of PD-1/PD-L1 inhibitors for advanced hepatocellular carcinoma[J]. Chinese Journal of Clinical Oncology, 2020, 47(5): 265-268. DOI: 10.3969/j.issn.1000-8179.2020.05.187
Authors:Jielang Li  Ting Chen  Yu Yang
Affiliation:Department of Abdominal Oncology, West China Hospital, Sichuan University, Chengdu 610000, China
Abstract:Systemic treatment of advanced hepatocellular carcinoma (HCC) includes targeted therapy, chemotherapy, and immunotherapy. In recent years, the treatment of advanced HCC has progressed with the use of programmed death receptor-1(PD-1)/programmed death receptor-1 ligand (PD-L1) inhibitors. Nivolumab and pembrolizumab have been approved by the US Food and Drug Administration (FDA) as a second-line treatment for advanced HCC. Multiple phase I/II clinical studies of PD-1/PD-L1 inhibitors combined with other systemic treatments have revealed good efficacy and safety. In a phase III clinical study, atezolizumab plus bevacizumab, as a new first-line treatment strategy, has been shown to be superior to the existing standard treatment (sorafenib). Here, we review the current research and progress in the use of PD-1/PD-L1 inhibitors for advanced HCC. 
Keywords:hepatocellular carcinoma  immunotherapy  PD-1 inhibitors  PD-L1 inhibitors
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