克罗恩病
医学
英夫利昔单抗
疾病
克罗恩病
内科学
随机对照试验
外科
作者
Casper Steenholdt,Jørn Brynskov,Ole Østergaard Thomsen,Lars Kristian Munck,Jan Fallingborg,Lisbet Ambrosius Christensen,Gitte Pedersen,Jens Kjeldsen,Bent A. Jacobsen,Anne Sophie Oxholm,Jakob Kjellberg,Klaus Bendtzen,Mark Ainsworth
出处
期刊:Gut
[BMJ]
日期:2013-07-22
卷期号:63 (6): 919-927
被引量:441
标识
DOI:10.1136/gutjnl-2013-305279
摘要
Although the reasons for secondary loss of response to infliximab (IFX) maintenance therapy in Crohn's disease vary, dose intensification is usually recommended. This study investigated the cost-effectiveness of interventions defined by an algorithm designed to identify specific reasons for therapeutic failure.Randomised, controlled, single-blind, multicentre study. 69 patients with secondary IFX failure were randomised to IFX dose intensification (5 mg/kg every 4 weeks) (n=36) or interventions based on serum IFX and IFX antibody levels using the proposed algorithm (n=33). Predefined co-primary end points at week 12 were proportion of patients responding (Crohn's Disease Activity Index (CDAI) decrease ≥ 70, or ≥ 50% reduction in active fistulas) and accumulated costs related to treatment of Crohn's disease, expressed as mean cost per patient, based on the Danish National Patient Registry for all hospitalisation and outpatient costs in the Danish healthcare sector.Costs for intention-to-treat patients were substantially lower (34%) for those treated in accordance with the algorithm than by IFX dose intensification: € 6038 vs € 9178, p<0.001. However, disease control, as judged by response rates, was similar: 58% and 53%, respectively, p=0.81; difference 5% (-19% to 28%). For per-protocol patients, treatment costs were even lower (56%) in the algorithm-treated group (€ 4062 vs € 9178, p<0.001) and with similar response rates (47% vs 53%, p=0.78; difference -5% (-33% to 22%)).Treatment of secondary IFX failure using an algorithm based on combined IFX and IFX antibody measurements significantly reduces average treatment costs per patient compared with routine IFX dose escalation and without any apparent negative effect on clinical efficacy.NCT00851565.
科研通智能强力驱动
Strongly Powered by AbleSci AI