Effectiveness and Safety of Advanced Combination Treatment (ACT) in patients with refractory inflammatory bowel disease or concomitant immune mediated disease or extra-intestinal manifestations: A Multi-Center Canadian Study.

IF 8 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Virginia Solitano, Ropo Ebenezer Ogunsakin, Yuhong Yuan, Charles N Bernstein, Talat Bessissow, Brian Bressler, Frank Hoentjen, Lisa van Lierop, Yvette Leung, Christopher MaMD, John Kenneth Marshall, Neeraj Narula, Mohammed Alahmari, Jeffrey D Mccurdy, Sanjay Murthy, Remo Panaccione, Greg Rosenfeld, Raquel Milgrom, Mark Silverberg, Vipul Jairath
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引用次数: 0

Abstract

Introduction: Due to the therapeutic ceiling associated with inflammatory bowel disease (IBD) therapies, some patients may require two advanced therapeutic agents, known as advanced combination treatment (ACT) to control disease or treat associated extraintestinal manifestations (EIMs).

Methods: We included adult IBD patients from 9 Canadian centers treated with either two biological therapies, a biological plus an oral small molecule, or two small molecules. Indications for ACT were: 1) refractory IBD; 2) uncontrolled immune mediated diseases (IMIDs); 3) uncontrolled EIMs. Primary outcomes were cumulative rates of clinical and endoscopic response and remission at 6 and 12 months. Secondary outcomes included serious adverse events and infections. Cox-proportional hazard analyses identified independent predictors of treatment effectiveness.

Results: We included 105 IBD patients (76 CD, 29 UC) with median age 35 (IQR 35.4-40.8). At baseline, 39% had perianal involvement, 58% had failed at least 3 advanced therapies and 40% had prior surgery. The primary reason for ACT was refractory IBD (63.8%), with the add-on approach used in 97.1% cases. The most frequent combination was anti-TNF + anti-integrin. At 12 months, cumulative rates of clinical and endoscopic response were 60.0% and 32.4%, respectively, and remission rates were 29.5% and 28.6%. Perianal disease was associated with reduced clinical remission (hazard ratio [HR] = 0.33, 95% confidence interval [CI]: 0.17-0.65, p = 0.001) and endoscopic response (HR = 0.42, 95% CI: 0.12-0.50, p=0.001). Longer disease duration (HR = 0.96, 95% CI: 0.92-0.99, p = 0.035) and baseline steroid use (HR = 0.39, p = 0.006) was associated with reduced clinical remission. Serious adverse events and infections occurred in 12.4% and 7.6% of patients, respectively.

Discussion: ACT was effective in achieving clinical and endoscopic outcomes in patients with refractory IBD or concomitant IMIDs/EIMs, with favorable safety profile.

高级联合治疗(ACT)在难治性炎症性肠病或伴发免疫介导疾病或肠外表现患者中的有效性和安全性:一项加拿大多中心研究
由于与炎症性肠病(IBD)治疗相关的治疗上限,一些患者可能需要两种高级治疗药物,称为高级联合治疗(ACT)来控制疾病或治疗相关的肠外表现(EIMs)。方法:我们纳入了来自加拿大9个中心的成年IBD患者,接受两种生物疗法,一种生物疗法加口服小分子疗法,或两种小分子疗法。ACT的适应症是:1)难治性IBD;2)未控制的免疫介导疾病(IMIDs);3)不受控制的eem。主要结果是6个月和12个月的临床和内窥镜反应和缓解的累积率。次要结局包括严重不良事件和感染。cox -比例风险分析确定了治疗效果的独立预测因子。结果:我们纳入了105例IBD患者(76例CD, 29例UC),中位年龄35岁(IQR 35.4-40.8)。基线时,39%的患者有肛周受累,58%的患者至少3次高级治疗失败,40%的患者有过术前手术。ACT的主要原因是难治性IBD(63.8%), 97.1%的病例使用了附加方法。最常见的组合是抗tnf +抗整合素。12个月时,临床和内镜下累积缓解率分别为60.0%和32.4%,缓解率为29.5%和28.6%。肛周疾病与临床缓解减少(风险比[HR] = 0.33, 95%可信区间[CI]: 0.17-0.65, p=0.001)和内镜下反应(风险比[HR] = 0.42, 95% CI: 0.12-0.50, p=0.001)相关。较长的病程(HR = 0.96, 95% CI: 0.92-0.99, p = 0.035)和基线类固醇使用(HR = 0.39, p = 0.006)与临床缓解减少相关。严重不良事件和感染发生率分别为12.4%和7.6%。讨论:ACT对难治性IBD或合并IMIDs/EIMs患者的临床和内窥镜结果有效,具有良好的安全性。
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来源期刊
American Journal of Gastroenterology
American Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
11.40
自引率
5.10%
发文量
458
审稿时长
12 months
期刊介绍: Published on behalf of the American College of Gastroenterology (ACG), The American Journal of Gastroenterology (AJG) stands as the foremost clinical journal in the fields of gastroenterology and hepatology. AJG offers practical and professional support to clinicians addressing the most prevalent gastroenterological disorders in patients.
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