Peng Tzu-Rong, Weng Yi-Fang, Wu Ta-Wei, Wu Chao-Chuan, Chou Yi-Chun, Hsu Ching-Sheng
Department of Pharmacy, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 231, Taiwan.
Department of Surgery, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 231, Taiwan.
Cancers (Basel). 2024 Aug 10;16(16):2813. doi: 10.3390/cancers16162813.
Although atezolizumab plus bevacizumab (hereinafter, atezolizumab-bevacizumab) is the standard first-line treatment for patients with advanced HCC, the optimal second-line regimen remains unknown. This study evaluated the efficacy and safety of sorafenib and lenvatinib in patients with advanced HCC that progressed under atezolizumab-bevacizumab treatment.
Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, we searched PubMed, Embase, and the Cochrane Library for articles published before November 2023. Random-effects meta-analysis was performed to determine the pooled objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS), comparing patients who received sorafenib versus lenvatinib.
Seven studies involving 387 patients were included. The pooled ORR, DCR, OS, and PFS for sorafenib and lenvatinib together were 26% (95% CI: 14-43%), 63% (95% CI: 47-77%), 11.45 months (95% CI: 7.12-15.77, = 92%, < 0.01), and 3.78 months (95% CI: 2.34-5.23, = 67%, = 0.02), respectively. Although lenvatinib users had a longer median OS (12.42 vs. 10.75 months) and PFS (5.15 vs. 2.58 months) than sorafenib users, the pooled ORR, DCR, median OS, and PFS for these medications were comparable. Additionally, the distributions of all-grade and grade ≥ 3 adverse events for sorafenib and lenvatinib were comparable to those for these two medications when used as first-line therapies.
Sorafenib or lenvatinib can provide effective treatment with manageable toxicity in patients with advanced HCC after disease progression under atezolizumab-bevacizumab.
尽管阿替利珠单抗联合贝伐珠单抗(以下简称阿替利珠单抗 - 贝伐珠单抗)是晚期肝癌患者的标准一线治疗方案,但最佳二线治疗方案仍不明确。本研究评估了索拉非尼和仑伐替尼在接受阿替利珠单抗 - 贝伐珠单抗治疗后病情进展的晚期肝癌患者中的疗效和安全性。
按照系统评价和Meta分析的首选报告项目指南,我们检索了PubMed、Embase和Cochrane图书馆中2023年11月之前发表的文章。进行随机效应Meta分析以确定接受索拉非尼与仑伐替尼治疗患者的汇总客观缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)和总生存期(OS)。
纳入了7项涉及387例患者的研究。索拉非尼和仑伐替尼联合治疗的汇总ORR、DCR、OS和PFS分别为26%(95%CI:14 - 43%)、63%(95%CI:47 - 77%)、11.45个月(95%CI:7.12 - 15.77,I² = 92%,P < 0.01)和3.78个月(95%CI:2.34 - 5.23,I² = 67%,P = 0.02)。尽管与使用索拉非尼的患者相比,使用仑伐替尼的患者中位OS(12.42对10.75个月)和PFS(5.15对2.58个月)更长,但这些药物的汇总ORR、DCR、中位OS和PFS具有可比性。此外,索拉非尼和仑伐替尼的所有级别和≥3级不良事件的分布与这两种药物作为一线治疗时的分布相当。
对于在阿替利珠单抗 - 贝伐珠单抗治疗后病情进展的晚期肝癌患者,索拉非尼或仑伐替尼可以提供有效治疗且毒性可控。