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Impact of infliximab therapy after early endoscopic recurrence following ileocolonic resection of Crohn's disease: a prospective pilot study.

机译:克罗恩病回结肠切除术后早期内镜复发后英夫利昔单抗治疗的影响:一项前瞻性研究。

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BACKGROUND: The efficacy of infliximab for endoscopic recurrence after resection of Crohn's disease (CD) has not yet been reported. The aim of this prospective study was to investigate the impact of infliximab on early endoscopic lesions after resection for CD. METHODS: Twenty-six patients maintaining clinical remission (CD activity index [CDAI] score <150) with mesalamine (3 g/day) after resection showed endoscopic recurrence in the neoterminal ileum at 6 months postoperatively (=baseline). Over the following 6 months, 10 patients were treated with continuous mesalamine (3 g/day), 8 patients were treated with azathioprine therapy (50 mg/day), and the other 8 patients were treated with infliximab therapy (5 mg/kg, every 8 weeks). During ileocolonoscopy at baseline and 6 months later, mucosal biopsies were taken for cytokine assays. RESULTS: During 6-month observation, no patients in the infliximab group, 3 (38%) in the azathioprine group, and 7 (70%) in the mesalamine group developed clinical recurrence (CDAI >or=150) (P = 0.01). At 6 months, endoscopic inflammation was improved in 75% of patients in the infliximab group, 38% in the azathioprine group, and 0% in the mesalamine group (P = 0.006). The mucosal interleukin (IL)-1beta, IL-6, and tumor necrosis factor-alpha levels significantly decreased in the infliximab group, while they significantly increased in the mesalamine group, and they did not change significantly in the azathioprine group. CONCLUSIONS: Infliximab therapy showed clear suppressive effects on clinical and endoscopic disease activity, and mucosal cytokine production in patients with early endoscopic lesions after resection. To confirm our conclusions, randomized controlled trials with a larger number of patients are necessary.
机译:背景:英夫利昔单抗对克罗恩病(CD)切除后内镜复发的疗效尚未见报道。这项前瞻性研究的目的是研究CD切除后英夫利昔单抗对早期内镜病变的影响。方法:26例在手术后6个月维持临床缓解(CD活性指数[CDAI]评分<150)并使用美沙拉敏(3 g /天)的患者在新末端回肠内镜下复发(基线)。在接下来的6个月中,有10例患者接受了连续的美沙拉敏治疗(3 g /天),有8例患者接受了硫唑嘌呤疗法(50 mg /天)治疗,其他8例患者接受了英夫利昔单抗治疗(5 mg / kg,每8周)。在基线的结肠结肠镜检查期间和6个月后,进行粘膜活检以进行细胞因子测定。结果:在6个月的观察期间,英夫利昔单抗组,硫唑嘌呤组3例,美沙拉敏组7例(70%)均未出现临床复发(CDAI> or = 150)(P = 0.01) 。在6个月时,英夫利昔单抗组75%的患者的内窥镜炎症得到改善,硫唑嘌呤组为38%,美沙拉敏组为0%(P = 0.006)。在英夫利昔单抗组中,粘膜白介素(IL)-1β,IL-6和肿瘤坏死因子-α水平显着降低,而在美沙拉敏组中则显着升高,而在硫唑嘌呤组中则没有显着变化。结论:英夫利昔单抗治疗对早期切除内镜病变患者的临床和内镜疾病活动以及黏膜细胞因子产生明显的抑制作用。为了证实我们的结论,需要对更多患者进行随机对照试验。

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