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分子靶向药物一线治疗肝细胞癌:一项倾向评分匹配分析

Primary Treatment with Molecular-Targeted Agents for Hepatocellular Carcinoma: A Propensity Score-matching Analysis.

作者信息

Nakano Masahito, Kuromatsu Ryoko, Niizeki Takashi, Okamura Shusuke, Iwamoto Hideki, Shimose Shigeo, Shirono Tomotake, Noda Yu, Kamachi Naoki, Koga Hironori, Torimura Takuji

机构信息

Division of Gastroenterology Department of Medicine Kurume University School of Medicine Kurume Japan.

出版信息

Hepatol Commun. 2020 Jun 20;4(8):1218-1228. doi: 10.1002/hep4.1535. eCollection 2020 Aug.

Abstract

Sorafenib and lenvatinib, as molecular-targeted agents, constitute effective primary treatment options for advanced hepatocellular carcinoma (HCC). However, the choice of optimal primary treatment agent remains controversial. Here, we aimed to assess the respective outcomes between these agents as primary treatment in patients with advanced HCC through use of propensity score-matching analysis (PSMA). We enrolled 670 consecutive patients who were diagnosed with advanced HCC and received sorafenib (n = 524) or lenvatinib (n = 146) as the primary treatment among 18 participating institutions between May 2009 and October 2019. To reduce confounding, we used PSMA regarding seven variables related to advanced HCC prognosis, resulting in the selection of 292 patients (n = 146 for each agent). Following PSMA, no significant difference was observed in the outcome of overall survival time between patients treated with sorafenib or lenvatinib (median survival time 15.3 or 14.9 months, respectively;  = 0.2358). Patients treated with lenvatinib exhibited significantly greater therapeutic effects (response rate: 5% and 31%; disease control rate: 46% and 69% for sorafenib and lenvatinib, respectively;  < 0.0001), but showed significantly lower probability of transition to secondary treatment (sorafenib, 60%; lenvatinib, 45%;  < 0.0269) and higher any adverse events rate (sorafenib, 86%; lenvatinib, 95%;  = 0.0207). : As a primary molecular-targeted agent-based treatment for advanced HCC, our findings suggested that sorafenib is generally appropriate as it offers significantly lower frequency of adverse events and higher probability of transition to secondary treatment, in consideration of the enhanced postprogression survival mediated by sequential treatment. Alternatively, lenvatinib affords a significantly higher therapeutic effect and should be used when immediate tumor reduction is required.

摘要

索拉非尼和仑伐替尼作为分子靶向药物,是晚期肝细胞癌(HCC)有效的一线治疗选择。然而,最佳一线治疗药物的选择仍存在争议。在此,我们旨在通过倾向评分匹配分析(PSMA)评估这些药物作为晚期HCC患者一线治疗的各自疗效。我们纳入了2009年5月至2019年10月期间在18个参与机构中连续诊断为晚期HCC并接受索拉非尼(n = 524)或仑伐替尼(n = 146)作为一线治疗的670例患者。为减少混杂因素,我们对与晚期HCC预后相关的7个变量进行PSMA,最终选择了292例患者(每种药物各146例)。PSMA后,接受索拉非尼或仑伐替尼治疗的患者总生存时间结果无显著差异(中位生存时间分别为15.3个月和14.9个月;P = 0.2358)。接受仑伐替尼治疗的患者表现出显著更高的治疗效果(缓解率:分别为5%和31%;疾病控制率:索拉非尼和仑伐替尼分别为46%和69%;P < 0.0001),但转为二线治疗的概率显著更低(索拉非尼,60%;仑伐替尼,45%;P < 0.0269),且任何不良事件发生率更高(索拉非尼,86%;仑伐替尼,95%;P = 0.0207)。作为晚期HCC基于分子靶向药物的一线治疗,我们的研究结果表明,考虑到序贯治疗介导的进展后生存延长,索拉非尼通常较为合适,因为它的不良事件发生率显著更低,转为二线治疗的概率更高。或者,仑伐替尼具有显著更高的治疗效果,当需要立即缩小肿瘤时应使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2590/7395064/7dbc1ca20465/HEP4-4-1218-g001.jpg

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