Randomised clinical trial: improvement in health outcomes with certolizumab pegol in patients with active Crohn’s disease with prior loss of response to infliximab

Aliment Pharmacol Ther 2011; 33: 541–550 Summary Background  Crohn’s disease (CD) is associated with impaired health‐related quality of life (HRQoL). Certolizumab pegol, administered either every 2 weeks (q2w) or q4w, maintains efficacy in patients previously failing on the anti‐TNF agent infliximab...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2011-03, Vol.33 (5), p.541-550
Hauptverfasser: Feagan, B. G., Sandborn, W. J., Wolf, D. C., Coteur, G., Purcaru, O., Brabant, Y., Rutgeerts, P. J.
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Sprache:eng
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Zusammenfassung:Aliment Pharmacol Ther 2011; 33: 541–550 Summary Background  Crohn’s disease (CD) is associated with impaired health‐related quality of life (HRQoL). Certolizumab pegol, administered either every 2 weeks (q2w) or q4w, maintains efficacy in patients previously failing on the anti‐TNF agent infliximab (WELCOME study). Aim  To investigate the impact of certolizumab pegol administered q2w and q4w on work productivity and HRQoL in the WELCOME study. Methods  Patients with loss of response to infliximab received open‐label certolizumab pegol induction and were randomised to receive double‐blind maintenance treatment with certolizumab pegol 400 mg either q4w or q2w through week 24, with a final evaluation at week 26. Work productivity and HRQoL were assessed using the Work Productivity and Activity Impairment:CD questionnaire and Inflammatory Bowel Disease Questionnaire respectively. Results  Baseline HRQoL burden was representative of moderately to severely active CD. HRQoL, daily activity and work productivity improved in both treatment groups as early as week 6 and were maintained through week 26. Treatment benefits to HRQoL, daily activity and work productivity were similar between the certolizumab pegol q2w vs. q4w groups. Conclusions  Certolizumab pegol therapy results in meaningful improvements in work productivity, daily activities and HRQoL in patients with active CD who previously responded to but either lost response or could not tolerate infliximab (ClinicalTrials.gov number: NCT00308581).
ISSN:0269-2813
1365-2036
DOI:10.1111/j.1365-2036.2010.04568.x