Efficacy of Infliximab after Failure of Subcutaneous Anti-TNF Agents in Patients with Moderate to Severe Ulcerative Colitis

N. Viazis, C. Pontas, G. Karampekos, E. Tsoukali, O. Giouleme, G. Theocharis, M. Tzouvala, A. Katsoula, M. Kalafateli, E. Zacharopoulou, E. Archavlis, Angeliki Chistidou, A. Manolakis, G. Mantzaris
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Abstract

Aim: To assess the efficacy of infliximab in ulcerative colitis (UC) patients who had failed therapy with adalimumab or golimumab. Methods: Retrospective analysis of prospectively acquired data of all anti-TNF naive patients with moderate to severe UC who received adalimumab or golimumab in 4 tertiary referral centres. Patients with primary non response or secondary loss of response to adalimumab or golimumab received therapy with infliximab. Clinical response and remission rates were assessed at week 14 and 54 after initiation of infliximab. Results: Between September 2015 and September 2017, 29 of 58 (50%) anti-TNF naive patients with moderate to severe UC failed therapy with adalimumab (n=38) or golimumab (n=20). Twenty one of 29 (72.4%) patients were primary non responders and 8 (27.6%) patients lost response to adalimumab or golimumab. All these 29 patients received infliximab, while 15 (51.7%) were on concomitant azathioprine therapy. Eighteen (62.1%) and 10 (34.5%) patients showed clinical response and clinical remission at week 14 respectively, while 14 (48.3%) patients were on clinical remission at week 54 after initiation of infliximab. Azathioprine co-administration at the start of infliximab was associated with a greater proportion of patients achieving clinical remission at week 54 (10 of 15 patients on combination therapy vs 4 of 14 patients on infliximab monotherapy, p=0.04). Conclusions: A significant proportion of anti-TNF naive patients with moderate to severe UC who have failed 1st course therapy with subcutaneous anti-TNF agents can achieve clinical response and/or remission with 2nd course therapy with infliximab.
英夫利昔单抗皮下抗肿瘤坏死因子治疗失败后对中重度溃疡性结肠炎患者的疗效观察
目的:评估英夫利昔单抗在阿达木单抗或戈利木单抗治疗失败的溃疡性结肠炎(UC)患者中的疗效。方法:回顾性分析在4个三级转诊中心接受阿达木单抗或戈利姆单抗治疗的所有抗tnf初治的中度至重度UC患者的前瞻性数据。对阿达木单抗或戈利姆单抗原发性无反应或继发性反应丧失的患者接受英夫利昔单抗治疗。在开始使用英夫利昔单抗后的第14周和第54周评估临床反应和缓解率。结果:在2015年9月至2017年9月期间,58例(50%)抗tnf初治的中重度UC患者中有29例(n=38)使用阿达木单抗(n=38)或戈利木单抗(n=20)治疗失败。29例患者中有21例(72.4%)为原发性无应答,8例(27.6%)患者对阿达木单抗或戈利木单抗失去应答。29例患者均接受英夫利昔单抗治疗,15例(51.7%)患者同时接受硫唑嘌呤治疗。18例(62.1%)和10例(34.5%)患者在第14周临床缓解,14例(48.3%)患者在开始使用英夫利昔单抗后第54周临床缓解。在英夫利昔单抗开始时联合给予硫唑嘌呤与在第54周获得临床缓解的患者比例较大相关(15例联合治疗患者中有10例,而14例英夫利昔单抗患者中有4例,p=0.04)。结论:有相当比例的抗tnf初治的中重度UC患者在第一个疗程的皮下抗tnf药物治疗失败后,可以通过英夫利昔单抗治疗第二个疗程获得临床缓解和/或缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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