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索拉非尼改善晚期肝细胞癌患者的生存:随机试验的荟萃分析。

Sorafenib improves the survival of patients with advanced hepatocellular carcinoma: a meta-analysis of randomized trials.

机构信息

Department of Oncology, PLA General Hospital of Chengdu Military Region, Chengdu, China.

出版信息

Anticancer Drugs. 2010 Mar;21(3):326-32. doi: 10.1097/CAD.0b013e3283350e26.

Abstract

There is no effective systemic therapy for patients with advanced hepatocellular carcinoma (HCC) except liver transplantation. Sorafenib, a multikinase inhibitor, has been shown to significantly increase overall survival (OS) in a randomized, placebo-controlled, phase III trial of patients with HCC (SHARP). The aim of this study was to evaluate the effectiveness of sorafenib for advanced HCC by carrying out a meta-analysis of randomized controlled trials that compared sorafenib-based therapy with other agent-based therapy. Randomized controlled trials comparing sorafenib or combined chemotherapy with placebo or combined chemotherapy in advanced HCC between 2000 and 2008 were identified and the data were extracted from reports. Outcomes analyzed were objective response rate, time to progression (TTP), OS, and toxicity. The summary hazard ratios (HRs), odds ratios, and their 95% confidence intervals (CIs) for mortality, objective response rate, and toxicity were estimated. All statistical tests were two-sided. Three trials including 924 patients were identified. Sorafenib-based chemotherapy was also associated with a 79% prolongation of TPP (HR = 0.58, 95% CI = 0.49-0.69, P<0.001), and a 37.3% increase in OS (HR = 0.66, 95% CI = 0.55-0.78, P<0.001). Despite significant increases in the frequencies of hand-foot syndrome and diarrhea in patients receiving sorafenib-containing chemotherapy, no significant difference in other toxic events was observed. This meta-analysis suggests that sorafenib-based chemotherapy is superior to placebo-based chemotherapy in terms of TPP and OS without increase in severe toxic effects.

摘要

对于晚期肝细胞癌(HCC)患者,除肝移植外,尚无有效的系统治疗方法。多激酶抑制剂索拉非尼在一项针对 HCC 患者的随机、安慰剂对照、III 期临床试验(SHARP)中已显示可显著延长总生存期(OS)。本研究旨在通过对比较索拉非尼为基础的治疗与其他基于药物的治疗的随机对照试验进行荟萃分析,评估索拉非尼在晚期 HCC 中的有效性。在 2000 年至 2008 年间,确定了比较索拉非尼或联合化疗与安慰剂或联合化疗治疗晚期 HCC 的随机对照试验,并从报告中提取数据。分析的结果包括客观缓解率、无进展生存期(TTP)、OS 和毒性。对死亡率、客观缓解率和毒性的汇总风险比(HR)、优势比及其 95%置信区间(CI)进行了估计。所有统计检验均为双侧。确定了三项包括 924 例患者的试验。基于索拉非尼的化疗还与 TPP 延长 79%(HR=0.58,95%CI=0.49-0.69,P<0.001)和 OS 增加 37.3%(HR=0.66,95%CI=0.55-0.78,P<0.001)相关。尽管接受含索拉非尼化疗的患者的手足综合征和腹泻频率显著增加,但其他毒性事件没有观察到显著差异。这项荟萃分析表明,基于索拉非尼的化疗在 TPP 和 OS 方面优于安慰剂为基础的化疗,而不会增加严重的毒性作用。

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