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首页> 外文期刊>Clinical gastroenterology and hepatology: the official clinical practice journal of the American Gastroenterological Association >Early trough levels and antibodies to infliximab predict safety and success of reinitiation of infliximab therapy
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Early trough levels and antibodies to infliximab predict safety and success of reinitiation of infliximab therapy

机译:早期谷水平和英夫利昔单抗抗体可预测英夫利昔单抗治疗的安全性和成功重新开始

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Background & Aims: Few agents are available for the treatment of inflammatory bowel diseases, and patients frequently become unresponsive to biologics. We investigated the feasibility of reinitiating infliximab therapy for patients who previously received only episodic therapy with, lost response to, or had infusion reactions to infliximab. We also aimed to identify factors associated with the success and safety of restarting infliximab, such as antibodies to infliximab and trough levels of the drug. Methods: From the inflammatory bowel disease biobank, we identified 128 consecutive patients (105 patients with Crohn's disease, 23 patients with ulcerative colitis) who restarted infliximab after a median 15-month discontinuation (range, 6-125 mo; 28 patients for loss of response or infusion reactions, 100 patients for remission or pregnancy). We also analyzed serum samples that had been collected during the first period of infliximab therapy (T-1), when therapy was reinitiated (T0), and at later time points (T+1, T+2) for trough levels and antibodies to infliximab. We investigated correlations among response to treatment, infusion reactions, treatment modalities, trough levels, and antibodies to infliximab. Results: Reinitiation of infliximab therapy produced a response in 84.5% of patients at week 14, 70% of patients at 1 year, and in 61% of patients at more than 4 years. Fifteen patients had acute infusion reactions and 10 patients had delayed infusion reactions. The absence of antibodies to infliximab at T+1 (hazard ratio [HR], 0.14; 95% confidence interval [CI], 0.026-0.74; P=.021) and reinitiation with concomitant immunomodulator therapy were associated with short-term responses (HR, 6.0; 95% CI, 1.3-27; P=.019). Pregnancy or remission as reason for discontinuation (HR, 2.70; 95% CI, 1.09-6.67; P=.033) and higher trough levels at T+1 (HR, 2.94; 95% CI, 1.18-7.69; P=.021) were associated with long-term response. Undetectable antibodies to infliximab at T+1 were associated with the safety of reinitiating therapy (HR for infusion reaction with detectable antibodies to infliximab, 7.7; 95% CI, 1.88-31.3; P=.004). Conclusions: Reinitiating infliximab therapy can be safe and effective for patients with Crohn's disease or ulcerative colitis after a median 15-month discontinuation period.
机译:背景与目的:很少有药物可用于治疗炎症性肠病,并且患者通常对生物制剂无反应。我们调查了对于以前仅接受偶发性治疗,对英夫利昔单抗无反应或有输注反应的患者,重新开始英夫利昔单抗治疗的可行性。我们还旨在确定与重启英夫利昔单抗的成功和安全性相关的因素,例如针对英夫利昔单抗的抗体和药物的谷值。方法:从炎症性肠病生物库中,我们确定了中位停药15个月(范围6-125 mo)后重新开始英夫利昔单抗的128例连续患者(105例克罗恩病,23例溃疡性结肠炎患者)。反应或输液反应,有100位患者缓解或怀孕)。我们还分析了在英夫利昔单抗治疗的第一个阶段(T-1),重新开始治疗(T0)以及以后的时间点(T + 1,T + 2)所采集的血清样品的谷水平和抗英夫利昔单抗。我们研究了对治疗,输注反应,治疗方式,谷水平和英夫利昔单抗抗体之间的相关性。结果:英夫利昔单抗治疗的重新开始在第14周时对84.5%的患者产生了反应,在1年时产生了70%的患者,超过4年的患者中产生了61%的患者。 15例有急性输注反应,10例有延迟输注反应。在T + 1时缺乏英夫利昔单抗的抗体(危险比[HR],0.14; 95%置信区间[CI],0.026-0.74; P = .021),并伴随免疫调节剂治疗的重新启动与短期反应相关( HR,6.0; 95%CI,1.3-27; P = .019)。妊娠或缓解是终止治疗的原因(HR,2.70; 95%CI,1.09-6.67; P = .033)和更高的T + 1谷水平(HR,2.94; 95%CI,1.18-7.69; P = .021) )与长期反应相关。在T + 1时检测不到的英夫利昔单抗抗体与重新开始治疗的安全性有关(与可检测到的英夫利昔单抗抗体的输注反应的HR为7.7; 95%CI为1.88-31.3; P = .004)。结论:中位停药15个月后,重新开始英夫利昔单抗治疗对于克罗恩病或溃疡性结肠炎患者是安全有效的。

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