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A randomised controlled trial of meloxicam, a Cox-2 inhibitor, to prevent hepatocellular carcinoma recurrence after initial curative treatment

机译:Cox-2抑制剂美洛昔康预防初始治愈性肝细胞癌复发的随机对照试验

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BackgroundBecause the recurrence rate of hepatocellular carcinoma (HCC) is high, even after curative treatments such as hepatic resection and microwave ablation, chemopreventive agents that can effectively suppress HCC recurrence are required. Cyclooxygenase-2 (Cox-2) was recently found to be overexpressed in HCC. Therefore, Cox-2 inhibitors may offer a chemopreventive therapy for HCC. This randomised controlled trial (RCT) investigated the potential for meloxicam, a clinically used Cox-2 inhibitor, to prevent HCC recurrence after initial curative treatment.MethodsA total of 232 consecutive patients underwent hepatic resection and/or microwave ablation as initial therapy for HCC at our institute between July 2008 and April 2011. Eight patients were excluded because of poor renal function, history of non-steroidal anti-inflammatory drug-related ulceration, or multiple cancers. The remaining 224 patients were randomised to a control group (n?=?113) or a meloxicam group (n?=?111). To patients in the meloxicam group, meloxicam was administered at 15?mg daily (5?mg three times a day) as long as possible. The overall survival (OS) and disease-free survival (DFS) rates were determined.ResultsThe 1-, 3-, and 5-year OS rates of the meloxicam group were 95.4, 82.4, and 70.1?%, respectively. Those of the control group were 98.2, 85.1, and 71.5?%, respectively (p?=?0.9549). The corresponding DFS rates of the meloxicam group were 89.2, 53.9, and 44.0?% and those of control group were 86.5, 57.0, and 43.4?%, respectively (p?=?0.6722). In the OS and DFS of subsets including patients with hepatitis B or C virus infection, we could not find significant differences between the meloxicam and control groups. However, in the subgroup of analysis of patients without viral hepatitis (NBNC-HCC), significant differences were observed in the DFS between the meloxicam group (1-year DFS, 92.3?%; 3-year DFS, 75.8?%; 5-year DFS, 70.4?%) and control group (1-year DFS, 83.3?%; 3-year DFS, 48.1?%; 5-year DFS, not obtained) (p?=?0.0211).ConclusionAdministration of the Cox-2 inhibitor meloxicam may have a possibility to suppress HCC recurrence after initial curative treatments in patients with NBNC-HCC.
机译:背景技术由于肝细胞癌(HCC)的复发率很高,即使经过肝切除和微波消融等治愈性治疗,也需要能有效抑制HCC复发的化学预防剂。最近发现环氧合酶2(Cox-2)在HCC中过表达。因此,Cox-2抑制剂可为HCC提供化学预防疗法。这项随机对照试验(RCT)研究了临床使用的Cox-2抑制剂美洛昔康在初次治愈后预防HCC复发的潜力。方法总共232例连续患者接受了肝切除和/或微波消融作为HCC的初始治疗。我们研究所于2008年7月至2011年4月之间。由于肾功能不佳,非甾体类抗炎药相关的溃疡病史或多种癌症而被排除在外的8例患者。其余224例患者被随机分为对照组(n = 113)或美洛昔康组(n = 111)。对于美洛昔康组的患者,美洛昔康每天尽可能以15?mg的剂量给药(每天3次,每次5?mg)。测定总生存率(OS)和无病生存率(DFS)。结果美洛昔康组的1年,3年和5年OS率分别为95.4%,82.4%和70.1%。对照组的分别为98.2%,85.1%和71.5%(p = 0.9549)。美洛昔康组相应的DFS率为89.2%,53.9%和44.0%,对照组的DFS率为86.5%,57.0%和43.4%(p = 0.6722)。在包括乙型或丙型肝炎病毒感染患者的亚组的OS和DFS中,我们未发现美洛昔康与对照组之间存在显着差异。但是,在无病毒性肝炎患者的分析亚组(NBNC-HCC)中,美洛昔康组之间的DFS差异显着(1年DFS为92.3%; 3年DFS为75.8%; 5-一年DFS,占70.4%;对照组(1年DFS,占83.3%; 3年DFS,占48.1%; 5年DFS,未获得)(p?=?0.0211)。 2抑制剂美洛昔康可能在NBNC-HCC患者进行初步治疗后抑制HCC复发。

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