4.7 Article

Randomised clinical trial: deep remission in biologic and immunomodulator naive patients with Crohn's disease - a SONIC post hoc analysis

期刊

ALIMENTARY PHARMACOLOGY & THERAPEUTICS
卷 41, 期 8, 页码 734-746

出版社

WILEY
DOI: 10.1111/apt.13139

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资金

  1. Abbott Laboratories
  2. Abbvie
  3. Aesca
  4. Janssen Biotech, Inc.
  5. Falk Pharma GmbH
  6. MSD
  7. AstraZeneca
  8. Merck Sharpe and Dohme
  9. Menarini
  10. Genesis
  11. Millenium/Takeda
  12. Santarus
  13. Prometheus
  14. Salix Pharmaceuticals
  15. Pfizer
  16. Bristol Myers Squibb
  17. Merck Research Laboratories
  18. UCB Pharma
  19. ActoGeniX NV
  20. AGI Therapeutics Inc
  21. Alba Therapeutics Corp
  22. Albireo
  23. Alfa Wasserman
  24. Amgen
  25. AM-Pharma BV
  26. Anaphore
  27. Astellas
  28. AthersysInc
  29. Atlantic Healthcare Ltd
  30. Aptalis
  31. BioBalance Corp
  32. BoehringerIngelheim
  33. Bristol-Myers Squibb
  34. Celgene
  35. Celek Pharmaceuticals
  36. Cellerix SL
  37. Cerimon Pharmaceuticals
  38. ChemoCentryx
  39. CoMentis
  40. Cosmo Technologies
  41. Coronado Biosciences
  42. Cytokine Pharmasciences
  43. Eagle Pharmaceuticals
  44. EnGeneInc
  45. Eli Lilly
  46. Enteromedics
  47. Exagen Diagnostics Inc
  48. Ferring Pharmaceuticals
  49. Flexio Therapeutics Inc
  50. Funxional Therapeutics Ltd
  51. Genzyme Corp
  52. Gilead Sciences
  53. Given Imaging
  54. GlaxoSmithKline
  55. Human Genome Sciences
  56. Ironwood Pharmaceuticals
  57. KaloBios Pharmaceuticals
  58. Lexicon Pharmaceuticals
  59. Lycera Corp
  60. Meda Pharmaceuticals
  61. Merck Serono
  62. Millenium Pharmaceuticals
  63. Nisshin Kyorin Pharmaceuticals
  64. Novo Nordisk
  65. NPS Pharmaceuticals
  66. Optimer Pharmaceuticals
  67. Orexigen Therapeutics Inc
  68. PDL Biopharma
  69. Procter and Gamble
  70. Prometheus Laboratories
  71. ProtAb Ltd
  72. Purgenesis Technologies Inc
  73. RelypsaInc
  74. Roche
  75. Salient Pharmaceuticals
  76. Schering Plough
  77. Shire Pharmaceuticals
  78. Sigmoid Pharma Ltd
  79. Sirtris Pharmaceuticals
  80. SLA Pharma UK Ltd
  81. Targacept
  82. Teva Pharmaceuticals
  83. Therakos
  84. TilliottsPharma AG
  85. TxCell SA
  86. Viamet Pharmaceuticals
  87. Vascular Biogenics Ltd
  88. Warner Chilcott UK Ltd
  89. Wyeth
  90. Genentech
  91. Janssen Pharmaceutical Research & Development, LLC
  92. Milennium Pharmaceuticals
  93. Novartis
  94. Johnson Johnson

向作者/读者索取更多资源

BackgroundAs treatment goals in Crohn's disease (CD) evolve, targets now include clinical remission (CR), mucosal healing (MH) and biological remission [C-reactive protein normalisation (CRPnorm)]. AimsTo evaluate the association of baseline factors and treatment with the achievement of different composite remission parameters at week 26. MethodsThis post hoc analysis of the SONIC trial evaluated different composite remission measures at week 26 in a subgroup of patients with Crohn's disease activity index (CDAI) scores, CRP, and endoscopic data available at baseline and week 26 (N=188). Assessed composite remission measures were: CR (CDAI<150) and MH (absence of any mucosal ulcerations), previously referred to as deep remission;' and alternative composite endpoints: CR+CRPnorm (CRP<0.8mg/dL); CRPnorm+MH; and CR+CRPnorm+MH. ResultsAmong analysed patients, 136/188 (72.3%) achieved CR and 90/188 (47.9%) achieved MH at week 26. All composite outcomes were significantly greater (Bonferroni significance level, P0.016) with combination therapy (i.e. infliximab and azathioprine; 52.3-63.6%) vs. azathioprine monotherapy (12.9-29.0%; p 0.005 for all comparisons). Composite remission rates including MH were significantly greater with combination therapy (52.3-56.9%) vs. infliximab (25.6-32.3%; P0.015 for all comparisons except CRPnorm+MH, P=0.017) and vs. azathioprine monotherapy (12.9-20.4%; P0.002 for all comparisons). Median serum trough infliximab concentrations among patients who achieved MH or CR+MH were greater when compared with those among patients who did not achieve MH (P=0.018) or CR+MH (P=0.053). Among the subgroup of patients with early Crohn's disease, MH alone or in combination with composite remission criteria significantly improved clinical outcomes of patients who received combination therapy. ConclusionsCombination therapy was more effective in achieving various composite remission measures vs. azathioprine or infliximab monotherapy. These data illustrate that deep remission' is achievable with combination therapy in a high percentage of patients with early Crohn's disease. ClinicalTrials.gov number: NCT00094458.

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