Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Curr Oncol. 2022 Sep 30;29(10):7305-7326. doi: 10.3390/curroncol29100575.
Chinese national guidelines recommend various systemic therapies for patients with advanced hepatocellular carcinoma (HCC), but optimal treatment selection remains uncertain. To summarize the evidence supporting the systemic treatment of Chinese patients with advanced HCC, we performed a systematic review using a literature search of PubMed, Embase, China National Knowledge Infrastructure, and the Chinese Scientific Journal Database between 1 January 2009 and 15 June 2021, and abstracts from ASCO 2020, ASCO GI 2021, ESMO 2020, and ESMO GI 2020. The inclusion criteria were: Chinese patients aged ≥18 years with advanced HCC; first- or second-line systemic therapy; an evaluation of the efficacy or safety outcomes; and a randomized controlled, non-randomized controlled, prospective, or retrospective design. Thirty reports were identified for the following therapies: the single-agent tyrosine kinase inhibitor (TKI; = 10), single-agent programmed death-1 (PD-1) inhibitor ( = 4), chemotherapy ( = 5), PD-1/programmed death-ligand 1 (PD-L1) inhibitor plus TKI ( = 6), PD-1/PD-L1 inhibitor plus bevacizumab or biosimilar ( = 4), and PD-1/PD-L1 inhibitor plus chemotherapy ( = 1). The heterogeneity between the studies precluded statistical analysis and the data were summarized using tables. In the first-line setting, evidence supported the use of atezolizumab or sintilimab plus bevacizumab or a biosimilar. There remains insufficient evidence to determine the optimal approved TKI-based therapeutic option, and active controlled trials in the second-line setting were lacking.
中国国家指南推荐了多种系统疗法用于治疗晚期肝细胞癌(HCC)患者,但最佳治疗选择仍不确定。为了总结支持中国晚期 HCC 患者系统治疗的证据,我们对 2009 年 1 月 1 日至 2021 年 6 月 15 日期间 PubMed、Embase、中国国家知识基础设施和中国科学期刊数据库中的文献进行了系统评价,同时还对 2020 年 ASCO、2021 年 ASCO GI、2020 年 ESMO 和 2020 年 ESMO GI 的摘要进行了检索。纳入标准为:年龄≥18 岁的中国晚期 HCC 患者;一线或二线系统治疗;评估疗效或安全性结局;随机对照、非随机对照、前瞻性或回顾性设计。共确定了 30 项报告,涉及以下治疗方法:单药酪氨酸激酶抑制剂(TKI; = 10)、单药程序性死亡受体-1(PD-1)抑制剂( = 4)、化疗( = 5)、PD-1/程序性死亡配体 1(PD-L1)抑制剂联合 TKI( = 6)、PD-1/PD-L1 抑制剂联合贝伐珠单抗或类似物( = 4)和 PD-1/PD-L1 抑制剂联合化疗( = 1)。由于研究之间存在异质性,因此无法进行统计学分析,数据采用表格进行总结。在一线治疗中,阿替利珠单抗或替雷利珠单抗联合贝伐珠单抗或类似物的证据支持其使用。目前尚无足够证据确定最佳的批准 TKI 治疗选择,二线治疗中缺乏活性对照试验。