Colman Ruben J, Rubin David T
Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, IL, USA
Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, IL, USA.
J Crohns Colitis. 2015 Apr;9(4):312-7. doi: 10.1093/ecco-jcc/jjv027. Epub 2015 Jan 23.
Methotrexate (MTX) is sometimes used as part of combination therapy for the treatment of inflammatory bowel disease [IBD]; however, the optimal MTX dose for combination therapy has not been established. This study compared the efficacy of lower-dose and higher-dose MTX with anti tumor necrosis factor alpha (anti-TNF) therapy among IBD patients.
Retrospective chart review was performed of 88 IBD patients at our center between 2010 and 2013. Low-dose MTX was defined as ≤ 12.5mg/week and high-dose MTX as 15-25mg/week. Patients who met the criteria for clinical remission [Harvey-Bradshaw Index ≤ 4, Simple Clinical Colitis Activity Index ≤ 2] at baseline were followed for up to 42 months. Chart review occurred in 6-month intervals. The primary outcome was consecutive months in remission prior to relapse. Secondary outcomes included other indicators of worsening disease [endoscopic inflammation, steroid use, therapy escalation/addition, or surgery] and adverse events. Regression analysis and Kaplan-Meier survival analysis were completed.
We identified 73 [83%] dual-therapy patients, of whom 32 low-dose and 14 high-dose individuals achieved remission. When compared with high-dose patients, low-dose patients were more likely to relapse [log-rank test, p < 0.01]. Secondary indicators of worsening disease occurred during 34.4% of low-dose review periods and 31.4% of high-dose review periods [p = 0.67]; 3/52 [6%] low-dose patients and 3/21 [14%] high-dose patients [p = 0.34] discontinued MTX therapy due to adverse events.
When combined with anti-TNF therapy, MTX at doses of >12.5mg/week was more effective at maintaining clinical remission than lower doses. These findings will guide management of combination therapy in IBD patients.
甲氨蝶呤(MTX)有时用作炎症性肠病(IBD)联合治疗的一部分;然而,联合治疗的最佳MTX剂量尚未确定。本研究比较了低剂量和高剂量MTX联合抗肿瘤坏死因子α(抗TNF)治疗在IBD患者中的疗效。
对2010年至2013年期间在本中心的88例IBD患者进行回顾性病历审查。低剂量MTX定义为≤12.5mg/周,高剂量MTX定义为15 - 25mg/周。符合基线临床缓解标准[哈维 - 布拉德肖指数≤4,简单临床结肠炎活动指数≤2]的患者随访长达42个月。病历审查每6个月进行一次。主要结局是复发前连续缓解的月数。次要结局包括疾病恶化的其他指标[内镜炎症、类固醇使用、治疗升级/添加或手术]和不良事件。完成回归分析和卡普兰 - 迈耶生存分析。
我们确定了73例[83%]联合治疗患者,其中32例低剂量和14例高剂量个体达到缓解。与高剂量患者相比,低剂量患者更易复发[对数秩检验,p < 0.01]。疾病恶化的次要指标在低剂量审查期的34.4%和高剂量审查期的31.4%出现[p = 0.67];3/52例[6%]低剂量患者和3/21例[14%]高剂量患者[p = 0.34]因不良事件停用MTX治疗。
与抗TNF治疗联合使用时,每周剂量>12.5mg的MTX在维持临床缓解方面比低剂量更有效。这些发现将指导IBD患者联合治疗的管理。