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首页> 外文期刊>BMC Cancer >Hepatic arterial infusion chemotherapy followed by sorafenib in patients with advanced hepatocellular carcinoma (HICS 55): an open label, non-comparative, phase II trial
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Hepatic arterial infusion chemotherapy followed by sorafenib in patients with advanced hepatocellular carcinoma (HICS 55): an open label, non-comparative, phase II trial

机译:晚期肝细胞癌(HICS 55)患者的肝动脉灌注化疗后加索拉非尼:一项开放性,非对照,II期临床研究

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In patients with advanced hepatocellular carcinoma (HCC), evidence is unclear as to whether hepatic arterial infusion chemotherapy (HAIC) or sorafenib is superior. We performed a prospective, open-label, non-comparative phase II study to assess survival with HAIC or HAIC converted to sorafenib. Fifty-five patients were prospectively enrolled. Patients received HAIC as a second course if they had complete response, partial response, or stable disease (SD) with an alpha fetoprotein (AFP) ratio 1 and a DCP ratio?>?1 or disease progression. The primary endpoint was the 1-year survival rate. Secondary endpoints were the 2-year survival rate, HAIC response, survival rate among HAIC responders, progression-free survival, and adverse events. Of the 55 patients in the intent-to-treat population, the 1-year and 2-year survival rates were 64.0 and 48.3%, respectively. After the first course of HAIC, one (1.8%) patient showed complete response, 13 (23.6%) showed partial response, 30 (54.5%) had SD, and 10 (18.1%) patients had progressive disease. Twenty-three patients (41.8%) had SD with AFP ratios 1 and DCP ratios >?1. Thirty-seven patients (68.5%) were responders and 17 (30.9%) were non-responders to HAIC. In responders, the 1-year and 2-year survival rates were 78 and 62%, respectively. Given the results of this study, this protocol deserves consideration for patients with advanced HCC. This trial was registered prospectively from December 12. 2012 to September 1. 2016.
机译:对于晚期肝细胞癌(HCC)患者,尚无证据表明肝动脉灌注化疗(HAIC)或索拉非尼是否更好。我们进行了一项前瞻性,开放标签,非比较性II期研究,以评估HAIC或HAIC转化为索拉非尼的生存率。前瞻性纳入了55名患者。如果患者有完全反应,部分反应或疾病稳定(SD)且甲胎蛋白(AFP)比率为1,DCP比率≥1或疾病进展,则接受HAIC作为第二个疗程。主要终点是1年生存率。次要终点为2年生存率,HAIC应答,HAIC应答者中的存活率,无进展生存期和不良事件。在意向性治疗人群中的55名患者中,1年和2年生存率分别为64.0%和48.3%。首次接受HAIC治疗后,有1名(1.8%)患者显示出完全缓解,有13名(23.6%)显示出部分缓解,有30名(54.5%)患有SD,有10名(18.1%)患有疾病进展。 23例(41.8%)的SD患者的AFP比率为1,DCP比率>≥1。对HAIC有37例患者(68.5%)有反应,而17例(30.9%)无反应。在应答者中,1年和2年生存率分别为78%和62%。鉴于这项研究的结果,该方案值得晚期HCC患者考虑。该试验的注册日期为2012年12月12日至2016年9月1日。

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