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每日一次 MMX(®)美沙拉嗪肠溶片用于溃疡性结肠炎内镜缓解的维持治疗。

Once-daily MMX(®) mesalamine for endoscopic maintenance of remission of ulcerative colitis.

机构信息

Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Am J Gastroenterol. 2012 Jul;107(7):1064-77. doi: 10.1038/ajg.2012.103. Epub 2012 May 8.

Abstract

OBJECTIVES

Treatment with mesalamine to maintain endoscopic remission (mucosal healing) of ulcerative colitis (UC) has been shown to reduce the risk of relapse and is the recommended first-line maintenance therapy. To improve treatment adherence, a mesalamine formulation that can be administered once-daily, MMX(®) mesalamine (Lialda; Shire Pharmaceuticals LLC, Wayne, PA), was developed. This study was conducted to determine the efficacy and safety of once-daily MMX mesalamine compared with twice-daily delayed-release mesalamine (Asacol; Warner Chilcott, Dublin, Ireland) for maintaining endoscopic remission in patients with UC.

METHODS

A multicenter, randomized, double-blind, 6-month, active-control trial was conducted to assess the non-inferiority of once-daily MMX mesalamine 2.4 g/day compared with twice-daily delayed-release mesalamine at a total daily dose of 1.6 g/day in patients with UC in endoscopic remission. The primary end point was maintenance of endoscopic remission at month 6 in the per-protocol (PP) population.

RESULTS

Overall, 826 patients were randomized and dosed. The primary objective (non-inferiority) was met. At month 6, 83.7 and 77.8% of patients receiving MMX mesalamine in the PP and intent-to-treat (ITT) populations, respectively, had maintained endoscopic remission compared with 81.5% (PP) and 76.9% (ITT) of patients receiving delayed-release mesalamine (95% confidence interval for difference: -3.9%, 8.1% (PP); -5.0%, 6.9% (ITT)). Time to relapse was not significantly different between the two treatment groups (log-rank test, P=0.5116 (PP); P=0.5455 (ITT)). The proportion of patients with adverse events was 37.1 and 36.0% in patients receiving MMX mesalamine and delayed-release mesalamine, respectively.

CONCLUSIONS

Once-daily dosing of MMX mesalamine 2.4 g/day was shown to be well tolerated and non-inferior to twice-daily dosing with delayed-release mesalamine 1.6 g/day for maintenance of endoscopic remission in patients with UC.

摘要

目的

采用美沙拉嗪维持溃疡性结肠炎(UC)内镜缓解(黏膜愈合)的治疗已被证明可降低复发风险,是推荐的一线维持治疗方法。为提高治疗依从性,开发了一种每天 1 次给药的美沙拉嗪制剂,即 MMX(®)美沙拉嗪(Lialda;Shire 制药公司,宾夕法尼亚州韦恩)。进行本项研究旨在确定与每天 2 次给予延迟释放型美沙拉嗪(Asacol;Warner Chilcott,都柏林,爱尔兰)相比,每天 1 次给予 MMX 美沙拉嗪治疗对维持 UC 内镜缓解的疗效和安全性。

方法

开展了一项多中心、随机、双盲、6 个月、活性对照试验,旨在评估在 UC 内镜缓解患者中,每天 1 次给予 MMX 美沙拉嗪 2.4 g/天与每天 2 次给予延迟释放型美沙拉嗪 1.6 g/天相比,前者非劣效于后者。主要终点为方案人群(PP)在第 6 个月时维持内镜缓解。

结果

共有 826 例患者被随机分组并接受治疗。主要目标(非劣效性)得到满足。在第 6 个月时,分别有 83.7%和 77.8%接受 MMX 美沙拉嗪治疗的 PP 人群和意向治疗(ITT)人群维持内镜缓解,而接受延迟释放型美沙拉嗪治疗的患者分别为 81.5%(PP)和 76.9%(ITT)(95%置信区间差值:-3.9%,8.1%(PP);-5.0%,6.9%(ITT))。两组之间复发时间无显著差异(对数秩检验,PP:P=0.5116;ITT:P=0.5455)。接受 MMX 美沙拉嗪和延迟释放型美沙拉嗪治疗的患者中,分别有 37.1%和 36.0%发生不良事件。

结论

每天 1 次给予 MMX 美沙拉嗪 2.4 g 治疗,与每天 2 次给予延迟释放型美沙拉嗪 1.6 g 治疗相比,耐受性良好且非劣效,可用于维持 UC 患者的内镜缓解。

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