Hindryckx P, Novak G, Vande Casteele N, Laukens D, Parker C, Shackelton L M, Narula N, Khanna R, Dulai P, Levesque B G, Sandborn W J, D'Haens G, Feagan B G, Jairath V
Robarts Clinical Trials Inc., University of Western Ontario, London, Ontario, Canada.
Department of Gastroenterology, University of Ghent, Ghent, Belgium.
Aliment Pharmacol Ther. 2017 Mar;45(5):617-630. doi: 10.1111/apt.13913. Epub 2017 Jan 11.
Although optimal medical management of acute severe ulcerative colitis (UC) is ill-defined, infliximab has become a standard of care. Accumulating evidence suggests an increased rate of infliximab clearance in patients with acute severe UC and a reduced colectomy rate with an intensified infliximab induction regimen.
To assess the strength of the current evidence for the relationship between infliximab pharmacokinetics, dosing strategies and disease behaviour in patients with acute severe UC.
We systematically searched MEDLINE and conference proceedings from 2000 to 2016 for relevant articles describing the pharmacokinetics of infliximab in acute severe UC and/or infliximab dose intensification strategies in acute severe UC. Eligible articles described randomised controlled trials, and cohort, cross-sectional, and case-controlled studies.
Of 400 citations identified, 76 studies were eligible. Increased infliximab clearance occurs in patients with acute severe UC, and is driven by the total inflammatory burden and leakage of drug into the colonic lumen. Several cohort studies suggest that infliximab dose intensification is beneficial to at least 50% of acute severe UC patients and the results of case-controlled studies indicate that an intensified infliximab dosing regimen with 1-2 additional infusions in the first 3 weeks of treatment could reduce the early (3-month) colectomy rate by up to 80%, although these data require prospective validation.
Uncontrolled studies suggest a benefit for infliximab dose optimisation in patients with acute severe UC. A randomised controlled trial in acute severe UC patients comparing a personalised infliximab dose-optimisation strategy with conventional dosing is a research priority.
尽管急性重症溃疡性结肠炎(UC)的最佳药物治疗方法尚不明确,但英夫利昔单抗已成为一种标准治疗方案。越来越多的证据表明,急性重症UC患者的英夫利昔单抗清除率增加,而强化英夫利昔单抗诱导方案可降低结肠切除术的发生率。
评估目前关于急性重症UC患者中英夫利昔单抗药代动力学、给药策略与疾病行为之间关系的证据强度。
我们系统检索了2000年至2016年期间的MEDLINE和会议论文集,以查找描述急性重症UC中英夫利昔单抗药代动力学和/或急性重症UC中英夫利昔单抗剂量强化策略的相关文章。符合条件的文章描述了随机对照试验、队列研究、横断面研究和病例对照研究。
在检索到的400篇文献中,有76项研究符合条件。急性重症UC患者中出现英夫利昔单抗清除率增加,这是由总的炎症负担和药物漏入结肠腔所驱动的。几项队列研究表明,英夫利昔单抗剂量强化对至少50%的急性重症UC患者有益,病例对照研究结果表明,在治疗的前3周增加1 - 2次英夫利昔单抗输注的强化给药方案可将早期(3个月)结肠切除术的发生率降低多达80%,尽管这些数据需要前瞻性验证。
非对照研究表明英夫利昔单抗剂量优化对急性重症UC患者有益。对急性重症UC患者进行一项随机对照试验,比较个性化英夫利昔单抗剂量优化策略与传统给药方案,是研究的重点。