Robarts Research Institute, The University of Western Ontario, London, ON, Canada.
Aliment Pharmacol Ther. 2010 Jun;31(12):1276-85. doi: 10.1111/j.1365-2036.2010.04303.x. Epub 2010 Mar 18.
The effect of certolizumab pegol on employment status and work productivity has not been previously assessed.
To assess the impact of treatment with certolizumab pegol, the only PEGylated, Fab' TNF antagonist, on work productivity in patients with active Crohn's disease (CD) from the PRECiSE 2 study.
Patients (n = 668) with active disease [CD activity index (CDAI) score of 220-450] were treated with open-label subcutaneous certolizumab pegol 400 mg (week 0, 2, 4). Responders (n = 425) (> or = 100-point decrease in CDAI from baseline) were randomized to receive certolizumab pegol 400 mg or placebo every 4 weeks until week 24, with final evaluation at week 26. Patients completed the Work Productivity and Activity Impairment for CD questionnaire (WPAI:CD) and the Inflammatory Bowel Disease Questionnaire (IBDQ) at weeks 0, 6, 16 and 26 and at the withdrawal visit.
Work productivity improved following induction with certolizumab pegol. Between week 6 and 26, certolizumab pegol-treated patients experienced significant improvement in work productivity compared with placebo recipients (11% and 10% overall improvement in work and activity impairment, respectively). During the maintenance phase, impairments in productivity and activities due to CD were significantly less in the certolizumab pegol group than in the placebo group.
Induction and maintenance therapy with certolizumab pegol significantly improved the work productivity of patients with active CD compared with those in the placebo group.
此前尚未评估培塞丽珠对就业状况和工作生产力的影响。
评估培塞丽珠(唯一的 PEG 化 Fab' TNF 拮抗剂)治疗对来自 PRECiSE 2 研究的活动期克罗恩病(CD)患者工作生产力的影响。
有活动期疾病(CD 活动指数 [CDAI] 评分 220-450)的患者(n=668)接受开放标签皮下培塞丽珠 400mg 治疗(第 0、2、4 周)。应答者(n=425,与基线相比 CDAI 下降≥100 分)被随机分配接受培塞丽珠 400mg 或安慰剂,每 4 周 1 次,直至第 24 周,最终评估在第 26 周进行。患者在第 0、6、16 和 26 周以及停药访视时完成工作生产力和 CD 活动障碍问卷(WPAI:CD)和炎症性肠病问卷(IBDQ)。
培塞丽珠诱导后工作生产力提高。在第 6 周到 26 周之间,与安慰剂组相比,培塞丽珠治疗组患者的工作生产力显著改善(总体工作和活动障碍分别改善 11%和 10%)。在维持阶段,培塞丽珠组患者的 CD 所致生产力和活动障碍明显低于安慰剂组。
与安慰剂组相比,培塞丽珠诱导和维持治疗可显著提高活动期 CD 患者的工作生产力。