Division of Gastroenterology, University of California San Diego, La Jolla, CA, USA. Division of Biomedical Informatics, University of California San Diego, La Jolla, CA, USA. Biostatistics Unit, Altman Clinical and Translational Research Institute, La Jolla, USA. Division of Epidemiology and Biostatistics, Western University, London, ON, Canada. Department of Medicine, Division of Gastroenterology, University Hospital, London, ON, Canada. Gastroenterology Unit, Amiens University and Hospital, Université de Picardie Jules Verne, Amiens, France. Department of Family Medicine and Public Health and Department of Mathematics, University of California San Diego, La Jolla, CA, USA.
Am J Gastroenterol. 2018 Aug;113(8):1197-1205. doi: 10.1038/s41395-018-0144-2. Epub 2018 Jun 21.
5-aminosalicylates (5-ASA) are frequently continued in patients with moderate-severe ulcerative colitis (UC), even after escalation to biologic agents, without evaluation of the benefit of this approach. We conducted an individual participant data (IPD) pooled analysis of trials of infliximab and golimumab in UC, to evaluate whether concomitant use of 5-ASA modifies clinical outcomes among anti-tumor necrosis factor (TNF)-α-treated patients.
We included IPD from five trials of infliximab and golimumab in patients with moderate-severe UC (ACT-1 and -2, PURSUIT-SC, PURSUIT-M, NCT00336492). Patients treated with infliximab or golimumab were categorized as receiving concomitant 5-ASA or not at time of trial entry. Primary outcome was clinical remission (Mayo Clinic Score < 3) at last follow-up for each trial; secondary outcomes were clinical response and mucosal healing. Using multivariable logistic regression analysis, we evaluated association between concomitant 5-ASA and clinical remission, after adjusting for sex, smoking, baseline disease activity, disease extent, biochemical variables (C-reactive protein, albumin, hemoglobin), and concomitant prednisone and immunomodulators.
We included 2183 infliximab-treated or golimumab-treated patients (1715 [78.6%] on 5-ASA). Concomitant use of 5-ASA was not associated with odds of achieving clinical remission (adjusted OR, 0.67 [95% CI, 0.45-1.01], p = 0.06), clinical response (aOR, 0.89 [0.60-1.33], p = 0.58) or mucosal healing (aOR, 1.12 [0.82-1.51], p = 0.48). These results were consistent in trials of induction and maintenance therapy, and in trials of infliximab and golimumab.
Based on IPD pooled analysis, in patients with moderate-severe UC who are escalated to anti-TNF therapy, continuing 5-ASA does not improve clinical outcomes.
5-氨基水杨酸(5-ASA)经常在中重度溃疡性结肠炎(UC)患者中继续使用,即使在升级为生物制剂后,也不评估这种方法的益处。我们对英夫利昔单抗和戈利木单抗治疗 UC 的试验进行了个体参与者数据(IPD)汇总分析,以评估在接受抗肿瘤坏死因子(TNF)-α 治疗的患者中,同时使用 5-ASA 是否会改变临床结局。
我们纳入了五项英夫利昔单抗和戈利木单抗治疗中重度 UC 的 IPD 试验(ACT-1 和 -2、PURSUIT-SC、PURSUIT-M、NCT00336492)。在试验入组时,接受英夫利昔单抗或戈利木单抗治疗的患者分为同时使用 5-ASA 和未同时使用 5-ASA。主要结局是每个试验的最后随访时的临床缓解(Mayo 评分<3);次要结局是临床应答和黏膜愈合。我们使用多变量逻辑回归分析,在调整性别、吸烟、基线疾病活动度、疾病范围、生化变量(C 反应蛋白、白蛋白、血红蛋白)和同时使用泼尼松和免疫调节剂后,评估同时使用 5-ASA 与临床缓解之间的关联。
我们纳入了 2183 名接受英夫利昔单抗或戈利木单抗治疗的患者(1715 名[78.6%]同时使用 5-ASA)。同时使用 5-ASA 与临床缓解的几率无关(调整后的比值比,0.67[95%CI,0.45-1.01],p=0.06),也与临床应答(调整后的比值比,0.89[0.60-1.33],p=0.58)或黏膜愈合(调整后的比值比,1.12[0.82-1.51],p=0.48)无关。这些结果在诱导和维持治疗的试验中以及英夫利昔单抗和戈利木单抗的试验中都是一致的。
基于 IPD 汇总分析,在中重度 UC 患者升级为抗 TNF 治疗后,继续使用 5-ASA 并不能改善临床结局。