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首页> 外文期刊>American Journal of Translational Research >Lenvatinib versus sorafenib as first-line therapy of advanced hepatocellular carcinoma: a systematic review and meta-analysis
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Lenvatinib versus sorafenib as first-line therapy of advanced hepatocellular carcinoma: a systematic review and meta-analysis

机译:Lenvatinib与Sorafenib为先进肝细胞癌的一线治疗:系统评价和荟萃分析

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There is limited evidence on the efficacy of lenvatinib in advanced hepatocellular carcinoma (HCC) patients. Aim of this meta-analysis was to compare lenvatinib and sorafenib as first-line treatment. Computerized bibliographic search was performed on main databases through November 2020. The primary outcome was overall survival, whereas survival rate (at 1-, and 2-year), progression-free survival (PFS), tumor response, and severe adverse event rate were the secondary outcomes. Results were expressed in terms of odds ratio (OR) or hazard ratio (HR) and 95% confidence interval (CI). Five studies enrolling 1481 patients were included. No difference in terms of overall survival was detected (HR 0.81, 0.58-1.11) and median survival was 13.4 months (9.38-17.48) in lenvatinib and 11.4 months (8.46-14.47) in sorafenib patients. Lenvatinib led to a significant improvement of PFS (HR 0.67, 0.48-0.94) and median PFS was 5.88 months (3.68-8) in lenvatinib and 4.17 months (3.08-5.25) in sorafenib patients. Lenvatinib determined a considerably higher rate of objective response (33.3%, 23.6%-43% versus 6.5%, 3.5%-9.5%; OR 7.70, 2.99-19.82), and of disease control rate (76.9%, 70.4%-83.5% versus 52.7%, 40.7%-64.6%; OR 2.41, 1.55-3.77). No difference between lenvatinib and sorafenib in terms of severe adverse event rate was observed (OR 1.31, 0.82-2.09). Lenvatinib prolongs progression-free survival as compared to sorafenib in HCC patients, although this result does not translate to a significant survival benefit.
机译:关于Lenvatinib在晚期肝细胞癌(HCC)患者的疗效存在有限的证据。该荟萃分析的目的是将Lenvatinib和Sorafenib与一线治疗进行比较。计算机化的书目搜索是在11月20日至2020年11月对主要数据库进行的。主要结果是总体生存,而存活率(1-和2年),无进展生存(PFS),肿瘤反应和严重不良事件率二次结果。结果表达了几率比(或)或危害比(HR)和95%置信区间(CI)。包括1481名患者的五项研究。未检测到整体存活方面的差异(HR 0.81,0.58-1.11)和中位存活是Lenvatinib中的13.4个月(9.38-17.48)和索拉非尼患者的11.4个月(8.46-14.47)。 Lenvatinib导致PFS的显着改善(HR 0.67,0.48-0.94),中位数PFS在Lenvatinib中的5.88个月(3.68-8),4.17个月(3.08-5.25)患者。 Lenvatinib确定了更高的客观反应速率(33.3%,23.6%-43%,比率为6.5%,3.5%-9.5%;或7.70,29.-19.82)和疾病控制率(76.9%,70.4%-83.5%与52.7%,40.7%-64.6%;或2.41,1.55-3.77)。 Lenvatinib和Sorafenib在观察到严重不良事件率的差异(或1.31,0.82-2.09)。 Lenvatinib与HCC患者中的索拉非尼相比,延长了无进展的生存期,尽管这种结果不转化为显着的生存效益。

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