4.6 Article

Implications of Infliximab Treatment Failure and Influence of Personalized Treatment on Patient-reported Health-related Quality of Life and Productivity Outcomes in Crohn's Disease

Journal

JOURNAL OF CROHNS & COLITIS
Volume 9, Issue 11, Pages 1032-1042

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ecco-jcc/jjv139

Keywords

IBD; infliximab; loss of response; quality of life; work; productivity; activity; indirect costs

Funding

  1. Aase and Ejnar Danielsen's Foundation
  2. Beckett Foundation
  3. Danish Biotechnology Program
  4. Danish Colitis-Crohn Society
  5. Danish Medical Association Research Foundation
  6. Frode V. Nyegaard and Wife's Foundation
  7. Health Science Research Foundation of Region of Copenhagen
  8. Herlev Hospital Research Council
  9. Lundbeck Foundation
  10. P. Carl Petersen's Foundation
  11. Ole Ostergaard Thomsen's Research Foundation
  12. Jorn Brynskov's Research Foundation

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Background: 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. Methods: 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. Results: 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. Conclusion: 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.

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