Gastroenterology Unit of Hospital La Princesa, Madrid, Spain.
J Clin Gastroenterol. 2011 Feb;45(2):113-8. doi: 10.1097/MCG.0b013e3181ebaef9.
The efficacy of infliximab therapy in patients with Crohn's disease (CD) is unknown beyond 12 months. For patients who lose their initial response, consideration can be given to dose "escalation" to regain therapeutic benefit.
Our primary goal was to evaluate the long-term durability of maintenance infliximab treatment. The secondary goals were to identify potential predictors of loss of infliximab efficacy, to evaluate the response to infliximab escalation, and the safety of the treatment with infliximab with and without escalation of dose.
CD patients treated with infliximab with response to an induction regimen were evaluated. Maintenance of long-term response was estimated using Kaplan-Meier analysis. The effect of specific variables was calculated using logistic regression analysis. Efficacy of dose escalation in patients who lose response to infliximab was analyzed.
Three hundred and nine CD patients were included. The mean follow-up time with infliximab treatment was 41 months, and the majority (95%) were on concomitant immunosuppressive therapy. The annual risk of loss of response to infliximab was 12% per patient-year of treatment. After loss of response, 41% of patients were managed with infliximab therapy escalation. After the first intensified dose, 56% of patients achieved remission and 40% partial response. Concurrent immunomodulators enhanced and smoking decreased the proportion of patients who maintained response (P<0.05).
A relevant proportion of CD patients on long-term infliximab treatment loss response. After loss of response, a high proportion of these patients initially respond to infliximab dose escalation. Concurrent immunomodulators may increase and smoking may decrease maintenance of response.
英夫利昔单抗治疗克罗恩病(CD)的疗效在 12 个月后尚不清楚。对于初始应答丧失的患者,可以考虑增加剂量以恢复治疗效果。
我们的主要目标是评估维持性英夫利昔单抗治疗的长期疗效。次要目标是确定丧失英夫利昔单抗疗效的潜在预测因素,评估英夫利昔单抗剂量升级的反应,以及评估剂量升级和不升级时英夫利昔单抗治疗的安全性。
评估对诱导治疗有应答的 CD 患者接受英夫利昔单抗治疗。采用 Kaplan-Meier 分析评估长期应答的维持情况。使用逻辑回归分析计算特定变量的影响。分析对英夫利昔单抗应答丧失的患者进行剂量升级的疗效。
共纳入 309 例 CD 患者。英夫利昔单抗治疗的中位随访时间为 41 个月,大多数(95%)患者同时接受免疫抑制治疗。每位患者每年因治疗而失去对英夫利昔单抗应答的风险为 12%。在失去应答后,41%的患者接受英夫利昔单抗治疗升级。在第一次强化剂量后,56%的患者达到缓解,40%达到部分缓解。同时使用免疫调节剂可增加、吸烟则降低维持应答的患者比例(P<0.05)。
相当一部分接受长期英夫利昔单抗治疗的 CD 患者会失去应答。在失去应答后,这些患者中有很大一部分最初对英夫利昔单抗剂量升级有应答。同时使用免疫调节剂可能会增加、吸烟则可能会降低维持应答的比例。