Division of Gastroenterology, University of Alberta, 130 University Campus NW, Edmonton, AB, T6G 2X8, Canada.
Dig Dis Sci. 2021 Nov;66(11):3985-3992. doi: 10.1007/s10620-020-06704-6. Epub 2020 Nov 13.
While there is recent literature to support the discontinuation of 5-aminosalicylate (5-ASA) upon the initiation of biologics, continuing 5-ASA after treatment failure is relatively common. We aimed to assess the impact of concomitant 5-ASA therapy on clinical outcomes in ulcerative colitis (UC) patients escalated to infliximab.
This is a retrospective chart review of patients with moderate-to-severe UC started on infliximab between January 2012 and December 2017 at the University of Alberta. The primary outcome was clinical remission (partial Mayo score < 2) at 6 and 12 months. Secondary outcomes included endoscopic (endoscopic Mayo < 2) and deep remission (combined clinical and endoscopic remission) as well as the need for rescue therapy, hospitalization or colectomy. Univariate and multivariate logistic regression models were used to estimate the odds ratios and 95% CI for the outcomes.
One hundred and twenty-one patients were followed over a period of 47 (SD = 34) months. Patients on 5-ASA had increased concomitant immunomodulator use (73.3% vs. 54.1%, p = 0.03). There was no difference in clinical remission at 6 (aOR 2.59, p = 0.07) or 12 months (aOR 0.43, p = 0.06). At 12 months, patients on concomitant 5-ASA were less likely to achieve endoscopic (aOR 0.08, p = 0.01) and deep remission (aOR 0.07, p = 0.02). Adverse outcomes such as need for rescue therapy, hospitalization, and colectomy did not differ between the groups.
Our data suggest that 5-ASA may be stopped in patients with moderate-to-severe UC who have been escalated to infliximab therapy as it has no additional benefit to control inflammation.
虽然有近期文献支持在开始使用生物制剂时停止使用 5-氨基水杨酸(5-ASA),但在治疗失败后继续使用 5-ASA 相对常见。我们旨在评估在升级至英夫利昔单抗的溃疡性结肠炎(UC)患者中,同时使用 5-ASA 治疗对临床结局的影响。
这是一项回顾性图表研究,纳入了 2012 年 1 月至 2017 年 12 月期间在阿尔伯塔大学接受英夫利昔单抗治疗的中重度 UC 患者。主要结局是 6 个月和 12 个月时的临床缓解(部分 Mayo 评分<2)。次要结局包括内镜缓解(内镜 Mayo<2)和深度缓解(临床和内镜缓解的联合)以及需要挽救治疗、住院或结肠切除术。采用单变量和多变量逻辑回归模型来估计结局的比值比和 95%CI。
共有 121 例患者接受了 47(SD=34)个月的随访。使用 5-ASA 的患者同时使用免疫调节剂的比例更高(73.3% vs. 54.1%,p=0.03)。6 个月(优势比 2.59,p=0.07)和 12 个月(优势比 0.43,p=0.06)时的临床缓解率无差异。在 12 个月时,使用同时使用 5-ASA 的患者更不可能达到内镜(优势比 0.08,p=0.01)和深度缓解(优势比 0.07,p=0.02)。两组之间的不良结局(如需要挽救治疗、住院和结肠切除术)无差异。
我们的数据表明,在升级至英夫利昔单抗治疗的中重度 UC 患者中,5-ASA 可能可以停用,因为它对控制炎症没有额外的益处。