Van Assche Gert, Magdelaine-Beuzelin Charlotte, D'Haens Geert, Baert Filip, Noman Maja, Vermeire Séverine, Ternant David, Watier Hervé, Paintaud Gilles, Rutgeerts Paul
Division of Gastroenterology, University of Leuven Hospitals, Leuven, Belgium.
Gastroenterology. 2008 Jun;134(7):1861-8. doi: 10.1053/j.gastro.2008.03.004. Epub 2008 Mar 8.
BACKGROUND & AIMS: The benefit to risk ratio of concomitant immunosuppressives with scheduled infliximab (IFX) maintenance therapy for Crohn's disease is an issue of debate. We aimed to study the influence of immunosuppressives discontinuation in patients in remission with combination therapy in an open-label, randomized, controlled trial.
Patients with controlled disease > or = 6 months after the start of IFX (5 mg/kg intravenously) combined with immunosuppressives were randomized to continue (Con) or to interrupt (Dis) immunosuppressives, while all patients received scheduled IFX maintenance therapy for 104 weeks. Primary end point was the proportion of patients who required a decrease in IFX dosing interval or stopped IFX therapy. Secondary end points included IFX trough levels, safety, and mucosal healing.
A similar proportion (24/40, 60% Con) and (22/40, 55% Dis) of patients needed a change in IFX dosing interval or stopped IFX therapy (11/40 Con, 9/40 Dis). C-reactive protein (CRP) was higher and IFX trough levels were lower in the Dis group (Dis: CRP, 2.8 mg/L; interquartile range [IQR], 1.0-8.0; Con: CRP, 1.6 mg/L; IQR, 1.0-5.6, P < .005; trough IFX: Dis: 1.65 microg/mL; IQR, 0.54-3.68; Con: 2.87 microg/mL; IQR, 1.35-4.72, P < .0001). Low IFX trough levels correlated with increased CRP and clinical score. Mucosal ulcers were absent at week 104 in 64% (Con) and 61% (Dis) of evaluated patients with ongoing response to IFX.
Continuation of immunosuppressives beyond 6 months offers no clear benefit over scheduled IFX monotherapy but is associated with higher median IFX trough and decreased CRP levels. The impact of these observations on long-term outcomes needs to be explored further.
对于克罗恩病患者,在定期使用英夫利昔单抗(IFX)维持治疗的同时联合使用免疫抑制剂,其获益风险比存在争议。我们旨在通过一项开放标签、随机对照试验,研究在联合治疗病情缓解的患者中停用免疫抑制剂的影响。
在开始使用IFX(静脉注射5mg/kg)联合免疫抑制剂治疗6个月及以上且病情得到控制的患者,被随机分为继续(Con)或中断(Dis)免疫抑制剂治疗组,而所有患者均接受为期104周的定期IFX维持治疗。主要终点是需要缩短IFX给药间隔或停止IFX治疗的患者比例。次要终点包括IFX谷浓度、安全性和黏膜愈合情况。
需要改变IFX给药间隔或停止IFX治疗的患者比例在两组中相似(继续治疗组24/40,60%;中断治疗组22/40,55%)(继续治疗组11/40,中断治疗组9/40)。中断治疗组的C反应蛋白(CRP)水平较高,IFX谷浓度较低(中断治疗组:CRP,2.8mg/L;四分位数间距[IQR],1.0 - 8.0;继续治疗组:CRP,1.6mg/L;IQR,1.0 - 5.6,P <.005;IFX谷浓度:中断治疗组:1.65μg/mL;IQR,0.54 - 3.68;继续治疗组:2.87μg/mL;IQR,1.35 - 4.72,P <.0001)。低IFX谷浓度与CRP升高和临床评分增加相关。在第104周时,对IFX持续有反应的评估患者中,64%(继续治疗组)和61%(中断治疗组)无黏膜溃疡。
免疫抑制剂使用超过6个月与单纯定期使用IFX单药治疗相比,并无明显益处,但与较高的IFX中位谷浓度和降低的CRP水平相关。这些观察结果对长期结局的影响需要进一步探讨。