He Shukang, Jiang Weichao, Fan Kai, Wang Xiaobei
Department of Clinical Laboratory, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Front Oncol. 2021 Mar 23;11:626984. doi: 10.3389/fonc.2021.626984. eCollection 2021.
Hepatocellular carcinoma (HCC) is often diagnosed at an advanced stage where only systemic treatment can be offered. The emergence of immune checkpoint inhibitors (ICIs) provides hope for the treatment of HCC. In this study, we performed a meta-analysis to provide evidence for the efficacy and safety of ICIs in the treatment of HCC.
The following databases and websites were searched: Embase, PubMed, Cochrane Library and ClinicalTrials.gov. The primary endpoints were response rate (RR), disease control rate (DCR), progression-free survival (PFS) and overall survival (OS).
Finally, twelve studies were included in this meta-analysis. When the corresponding outcome indicators and their 95% confidence intervals (CIs) were pooled directly, the overall RR, DCR, PFS and OS were 0.17 (0.15-0.19, I = 56.2%, P=0.009), 0.58 (0.55-0.61, I = 75.9%, P<0.001), 3.27 months (2.99-3.55, I = 73.0%, P=0.001), 11.73 months (10.79-12.67, I = 90.3%, P<0.001). Compared to the control group, treatment with ICIs significantly improved RR, PFS and OS, the OR and HRs were 3.11 (2.17-4.44, P<0.001), 0.852 (0.745-0.974, P=0.019) and 0.790 (0.685-0.911, P=0.001), respectively. However, no significant improvement in DCR was found in ICIs treatment in this meta-analysis.
HCC patients would benefit from ICIs treatment, however, more studies are needed in the future to provide more useful evidence for the treatment of HCC by programmed death-1 (PD-1) or programmed death ligand 1 (PD-L1) inhibitors.
肝细胞癌(HCC)常于晚期才被诊断出来,此时往往只能进行全身治疗。免疫检查点抑制剂(ICIs)的出现为HCC的治疗带来了希望。在本研究中,我们进行了一项荟萃分析,以提供ICIs治疗HCC的疗效和安全性证据。
检索了以下数据库和网站:Embase、PubMed、Cochrane图书馆和ClinicalTrials.gov。主要终点为缓解率(RR)、疾病控制率(DCR)、无进展生存期(PFS)和总生存期(OS)。
最终,12项研究纳入了本荟萃分析。直接汇总相应的结局指标及其95%置信区间(CIs)时,总体RR、DCR、PFS和OS分别为0.17(0.15 - 0.19,I = 56.2%,P = 0.009)、0.58(0.55 - 0.61,I = 75.9%,P < 0.001)、3.27个月(2.99 - 3.55,I = 73.0%,P = 0.001)、11.73个月(10.79 - 12.67,I = 90.3%,P < 0.001)。与对照组相比,ICIs治疗显著改善了RR、PFS和OS,OR和HR分别为3.11(2.17 - 4.44,P < 0.001)、0.852(0.745 - 0.974,P = 0.019)和0.790(0. / 685 - 0.911,P = 0.001)。然而,在本荟萃分析中,ICIs治疗未发现DCR有显著改善。
HCC患者将从ICIs治疗中获益,然而,未来还需要更多研究,以提供关于程序性死亡受体1(PD - 1)或程序性死亡配体1(PD - L1)抑制剂治疗HCC的更有用证据。