She Mingjin, Wu Yayun, Cheng Mengmeng, Feng Sanli, Li Guizhi, Rong Hui
Department of Oncology, The Anhui Provincial Corps Hospital of Chinese People's Armed Police Forces, Hefei, China.
Front Med (Lausanne). 2024 May 2;11:1401139. doi: 10.3389/fmed.2024.1401139. eCollection 2024.
To systematically evaluate the safety and efficacy of PD-1/PD-L1 inhibitor-based immunotherapy (hereafter referred to as "combination immunotherapy") compared with that of sorafenib in the treatment of hepatocellular carcinoma (HCC).
Databases such as PubMed, Embase, and the Cochrane Library were searched from the date of their establishment to September 2023 to identify randomized controlled trials (RCTs) of combination immunotherapy versus sorafenib for the treatment of advanced HCC. Two reviewers independently evaluated the quality of the included studies, extracted the data, and cross-checked the information. The meta-analysis was performed using RevMan 5.3 software.
A total of 5 RCTs were included. The results of the meta-analysis showed the following: (1) Effectiveness. Compared to sorafenib, combination immunotherapy significantly improved overall survival (OS, HR = 0.69, 95% CI: 0.58 ~ 0.82, < 0.01) and progression-free survival (PFS, HR = 0.62, 95% CI: 0.50 ~ 0.78, < 0.001) in patients with advanced HCC. (2) Safety. Both groups had comparatively high incidences of adverse events (AEs), but the difference in any treatment-related adverse events was not significant between the two arms (OR = 0.98, 95% CI: 0.95 ~ 1.02, = 0.34). The difference in the incidence of grade 1-2 adverse reactions was statistically significant (OR = 0.66, 95% CI = 0.49-0.90, = 0.001). There were no differences in grade 3/4 TRAEs or grade 5 TRAEs (OR = 1.46, 95% CI = 0.78 ~ 2.71, = 0.24; OR = 1.08, 95% CI = 0.73 ~ 1.58, = 0.71).
Combined immunotherapy can significantly prolong the OS and PFS of patients with advanced HCC without increasing the incidence of adverse effects in terms of safety, but the incidence of AEs in different systems is different.
系统评价与索拉非尼相比,基于程序性死亡受体1(PD-1)/程序性死亡配体1(PD-L1)抑制剂的免疫疗法(以下简称“联合免疫疗法”)治疗肝细胞癌(HCC)的安全性和疗效。
检索PubMed、Embase和Cochrane图书馆等数据库,检索时间从建库至2023年9月,以确定联合免疫疗法与索拉非尼治疗晚期HCC的随机对照试验(RCT)。两名研究者独立评估纳入研究的质量,提取数据并交叉核对信息。使用RevMan 5.3软件进行荟萃分析。
共纳入5项RCT。荟萃分析结果显示:(1)有效性。与索拉非尼相比,联合免疫疗法显著改善了晚期HCC患者的总生存期(OS,风险比[HR]=0.69,95%置信区间[CI]:0.580.82,P<0.01)和无进展生存期(PFS,HR=0.62,95%CI:0.500.78,P<0.001)。(2)安全性。两组不良事件(AE)发生率均较高,但两组间任何治疗相关不良事件的差异均无统计学意义(比值比[OR]=0.98,95%CI:0.951.02,P=0.34)。12级不良反应发生率的差异有统计学意义(OR=0.66,95%CI=0.490.90,P=0.001)。3/4级治疗相关不良事件(TRAE)或5级TRAE无差异(OR=1.46,95%CI=0.782.71,P=0.24;OR=1.08,95%CI=0.73~1.58,P=0.71)。
联合免疫疗法可显著延长晚期HCC患者的OS和PFS,且在安全性方面未增加不良反应的发生率,但不同系统的AE发生率有所不同。