Department of Gastroenterology, Austin Hospital, Melbourne, Australia.
Department of Gastroenterology, St Vincent's Hospital, Melbourne, Australia.
Inflamm Bowel Dis. 2019 Jun 18;25(7):1169-1186. doi: 10.1093/ibd/izy383.
Infliximab is an effective salvage therapy in acute severe ulcerative colitis; however, the optimal dosing strategy is unknown. We performed a systematic review and meta-analysis to examine the impact of infliximab dosage and intensification on colectomy-free survival in acute severe ulcerative colitis.
Studies reporting outcomes of hospitalized steroid-refractory acute severe ulcerative colitis treated with infliximab salvage were identified. Infliximab use was categorized by dose, dose number, and schedule. The primary outcome was colectomy-free survival at 3 months. Pooled proportions and odds ratios with 95% confidence intervals were reported.
Forty-one cohorts (n = 2158 cases) were included. Overall colectomy-free survival with infliximab salvage was 79.7% (95% confidence interval [CI], 75.48% to 83.6%) at 3 months and 69.8% (95% CI, 65.7% to 73.7%) at 12 months. Colectomy-free survival at 3 months was superior with 5-mg/kg multiple (≥2) doses compared with single-dose induction (odds ratio [OR], 4.24; 95% CI, 2.44 to 7.36; P < 0.001). However, dose intensification with either high-dose or accelerated strategies was not significantly different to 5-mg/kg standard induction at 3 months (OR, 0.70; 95% CI, 0.39 to 1.27; P = 0.24) despite being utilized in patients with a significantly higher mean C-reactive protein and lower albumin levels.
In acute severe ulcerative colitis, multiple 5-mg/kg infliximab doses are superior to single-dose salvage. Dose-intensified induction outcomes were not significantly different compared to standard induction and were more often used in patients with increased disease severity, which may have confounded the results. This meta-analysis highlights the marked variability in the management of infliximab salvage therapy and the need for further studies to determine the optimal dose strategy.
英夫利昔单抗是急性重度溃疡性结肠炎的有效挽救疗法;然而,最佳剂量策略尚不清楚。我们进行了系统评价和荟萃分析,以研究英夫利昔单抗剂量和强化治疗对急性重度溃疡性结肠炎无结肠切除生存的影响。
确定了报告接受英夫利昔单抗挽救治疗的住院类固醇难治性急性重度溃疡性结肠炎患者结局的研究。根据剂量、剂量数和方案对英夫利昔单抗的使用进行分类。主要结局是 3 个月时无结肠切除的生存。报告了合并比例和 95%置信区间的比值比。
纳入了 41 项队列(n = 2158 例)。英夫利昔单抗挽救后的总体无结肠切除生存在 3 个月时为 79.7%(95%置信区间 [CI],75.48%至 83.6%),在 12 个月时为 69.8%(95% CI,65.7%至 73.7%)。与单次剂量诱导相比,5mg/kg 多次(≥2 次)剂量在 3 个月时具有更好的无结肠切除生存(比值比 [OR],4.24;95% CI,2.44 至 7.36;P < 0.001)。然而,高剂量或加速策略的剂量强化在 3 个月时与 5mg/kg 标准诱导没有显著差异(OR,0.70;95% CI,0.39 至 1.27;P = 0.24),尽管在疾病严重程度明显较高的患者中使用了这些策略,这可能使结果复杂化。
在急性重度溃疡性结肠炎中,多次 5mg/kg 英夫利昔单抗剂量优于单次剂量挽救。与标准诱导相比,剂量强化诱导的结果没有显著差异,并且在疾病严重程度增加的患者中更常使用,这可能使结果复杂化。这项荟萃分析强调了英夫利昔单抗挽救治疗管理的显著变异性,需要进一步研究以确定最佳剂量策略。