4.7 Review

Review article: a clinician's guide for therapeutic drug monitoring of infliximab in inflammatory bowel disease

期刊

ALIMENTARY PHARMACOLOGY & THERAPEUTICS
卷 38, 期 5, 页码 447-459

出版社

WILEY-BLACKWELL
DOI: 10.1111/apt.12407

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资金

  1. Abbott
  2. Alba
  3. Axcan
  4. Bristol Myers Squibb
  5. Centocor
  6. Ferring
  7. GSK
  8. Genentec
  9. Merck
  10. Millennium
  11. Novartis
  12. Otsuka
  13. Proctor Gamble
  14. Roche
  15. VSL#3
  16. UCB Pharma
  17. Centocor Inc
  18. Millennium Pharmaceuticals
  19. Janssen Canada
  20. Prometheus Laboratories
  21. Abbott Laboratories
  22. Amgen
  23. AstraZeneca
  24. Aptalis
  25. Biogen Idec
  26. Bristol-Myers Squibb
  27. ChemoCentryx
  28. Eisai Medical Research Inc
  29. Elan Pharmaceuticals
  30. Genetech
  31. GlaxoSmithKline
  32. Janssen
  33. Merck Sharp and Dohme Corp
  34. Takeda
  35. Ocera Therapeutics Inc.
  36. Otsuka America Pharmaceutical
  37. Pfizer
  38. Shire Pharmaceuticals
  39. Schering-Plough
  40. Synta Pharmaceuticals Corp
  41. Teva
  42. Warner Chilcott
  43. AbbVie
  44. Janssen Inc.
  45. Prometheus Labs
  46. MSD
  47. Zealand Pharma
  48. Millenium/Takeda
  49. Abbott/AbbVie
  50. Genentech
  51. Glaxo Smith Kline
  52. Procter and Gamble Pharmaceuticals
  53. ActoGeniX
  54. CombinatoRx
  55. Elan/Biogen
  56. Protein Design Labs
  57. Tillotts
  58. Wyeth

向作者/读者索取更多资源

Background Tumour necrosis factor (TNF)-antagonists have an established role in the treatment of inflammatory bowel diseases (IBDs), however, subtherapeutic drug levels and the formation of anti-drug antibodies (ADAs) may decrease their efficacy. Aim The evidence supporting the use of therapeutic drug monitoring (TDM) based clinical algorithms for infliximab (IFX) and their role in clinical practice will be discussed. Methods The literature was reviewed to identify relevant articles on the measurement of IFX levels and antibodies-to-infliximab. Results Treatment algorithms for IBD have evolved from episodic monotherapy used in patients refractory to all other treatments, to long-term combination therapy initiated early in the disease course. Improved remission rates have been observed with this paradigm shift, nevertheless many patients ultimately lose response to therapy. Although empiric dose optimization or switching agents constitute the current standard of care for secondary failure, these interventions have not been applied in an evidence-based manner and are probably not cost-effective. Multiple TDM-based algorithms have been developed to identify patients that may benefit from measurement of IFX and ADA levels to guide adjustments to therapy. Conclusions Therapeutic drug monitoring offers a rational approach to the management of secondary failure to IFX. This concept has gained momentum based on evidence from case series, cohort studies and post-hoc analyses of randomised controlled trials.

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