Department of Gastroenterology, Herlev Hospital, Herlev, Denmark
Department of Gastroenterology, Herlev Hospital, Herlev, Denmark.
J Crohns Colitis. 2015 Nov;9(11):1032-42. doi: 10.1093/ecco-jcc/jjv139. Epub 2015 Aug 5.
This study assessed the effects of infliximab (IFX) treatment failure on patient-reported outcomes and explored the influence of using personalized treatment in this situation.
Sixty-nine Crohn's disease patients with IFX treatment failure were randomized to an intensified IFX regimen (n = 36) or personalized treatment defined by IFX and anti-IFX antibodies (n = 33). Health-related quality of life evaluated with the Short Inflammatory Bowel Disease Questionnaire (IBDQ) and productivity evaluated with the Work Productivity and Activity Impairment Questionnaire (WPAI:CD) were assessed at treatment failure and after 4, 8, 12 and 20 weeks.
Median IBDQ score at manifestation of IFX treatment failure was 40 and improved markedly in responders by 11 at weeks 4 and 8 (p < 0.001) and by 13 at weeks 12 and 20 (p < 0.001). Non-responders improved modestly at weeks 12 and 20 (increase of median 4, p < 0.05). Overall activity impairment was high at IFX failure (median 70%) and decreased substantially in responders (40-50%, p < 0.001) and to a lesser extent in non-responders (15-40%, p < 0.05). In employed patients (55%), absenteeism was negligible during the entire study period. However, median presenteeism was 40% at manifestation of IFX failure and decreased only among responders across time (decrease 10-30%, p < 0.05). Although anti-tumour necrosis factor (TNF) therapy was discontinued in most patients handled by personalized treatment, IBDQ and WPAI:CD scores were similar in these patients compared with patients routinely dose-intensified on IFX.
Regaining low disease activity after IFX failure is necessary for minimizing patient impairment and indirect disease-related costs. A personalized treatment strategy does not have a negative influence on patient-reported outcomes.
本研究评估了英夫利昔单抗(IFX)治疗失败对患者报告结局的影响,并探讨了在此情况下使用个体化治疗的影响。
69 例 IFX 治疗失败的克罗恩病患者被随机分为强化 IFX 方案组(n=36)或个体化治疗组(n=33),个体化治疗定义为 IFX 和抗 IFX 抗体。采用短肠病问卷(IBDQ)评估健康相关生活质量,采用工作生产效率和活动障碍问卷(WPAI:CD)评估工作生产效率。在 IFX 治疗失败时以及治疗后 4、8、12 和 20 周进行评估。
IFX 治疗失败时的 IBDQ 评分中位数为 40 分,应答者在治疗后 4 周和 8 周时分别显著提高 11 分(p<0.001),在治疗后 12 周和 20 周时分别提高 13 分(p<0.001)。无应答者在治疗后 12 周和 20 周时略有改善(中位数增加 4,p<0.05)。IFX 治疗失败时活动障碍程度较高(中位数为 70%),应答者的活动障碍显著降低(40%-50%,p<0.001),无应答者的活动障碍程度降低程度较小(15%-40%,p<0.05)。在在职患者(55%)中,整个研究期间缺勤率可忽略不计。然而,IFX 治疗失败时的中位工作投入度为 40%,仅应答者随着时间的推移而减少(减少 10%-30%,p<0.05)。尽管大多数接受个体化治疗的患者停用了抗肿瘤坏死因子(TNF)治疗,但这些患者的 IBDQ 和 WPAI:CD 评分与常规剂量强化 IFX 治疗的患者相似。
IFX 治疗失败后恢复低疾病活动度对于将患者的损害和间接疾病相关成本降至最低是必要的。个体化治疗策略对患者报告结局没有负面影响。