Abstract

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.

Highlights

  • Hepatocellular carcinoma (HCC) is globally known as a highly malignant tumor with poor prognosis [1]

  • We evaluated the effectiveness of Cox-2 inhibitors as prevention of hepatocellular carcinoma (HCC) recurrence, comparing meloxicam, a Cox-2 inhibitor, versus control in patients with HCC who underwent hepatic resection and/or microwave coagulo-necrotic therapy (MCN)

  • The reasons for discontinuation in 38 patients included: reduced renal function (n = 12), gastrointestinal tract ulcer (n = 5), exacerbation of disease (n = 4), prolonged postoperative complications (n = 2), cough (n = 1), cerebral infarction (n = 1), poor adherence (n = 5), other cancer break out (n = 1), and discontinuation judged by physician (n = 7)

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Summary

Introduction

Hepatocellular carcinoma (HCC) is globally known as a highly malignant tumor with poor prognosis [1]. In Japan, hepatic resection and local ablative therapies are recommended for small HCCs involving three nodules or less with a diameter of 3 cm at most; it frequently recurs after 5 years post treatment. Since hepatic resection and ablative therapies are still performed as the treatment of choice, measures to prevent recurrence are required. Because 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. 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

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