[Predictors of efficacy, mucosal healing and dose intensification during the first year of adalimumab therapy in patients with luminal and fistulizing Crohn's disease. National data from Hungary]

Orv Hetil. 2011 Sep 4;152(36):1433-42. doi: 10.1556/OH.2011.29200.
[Article in Hungarian]

Abstract

Adalimumab is a fully human monoclonal antibody targeting tumor necrosis factor with proven efficacy in the treatment of Crohn's disease in clinical trials. The aim of the present study was to investigate the predictors of medium term clinical efficacy and mucosal healing during adalimumab therapy in patients with Crohn's disease in specialized centers approved for biological therapy in Hungary.

Methods: Data of 201 Crohn's disease patients were prospectively captured (male/female: 112/89, median age: 24 years, duration: 8 years). Previous infliximab therapy was given in 97 (48.3%) patients, concomitant steroids in 41.3% and azathioprine in 69.2% (combined: 26.4%) of patients.

Results: Overall clinical response and remission rates at 24 and 52 weeks were 78% and 52%, and 69.4% and 44.4%, respectively. Endoscopic improvement and healing was achieved in 43.1% and 23.6%, respectively. In a logistic regression model, clinical efficacy and normalized C-reactive protein at week 12, need for combined immunosuppression at induction, shorter disease duration and smoking were identified as independent predictors for 12-month clinical outcome, while normalized C-reactive protein at week 12, clinical remission at week 24, frequency of previous relapses and smoking were associated to endoscopic improvement/healing. Dose intensification to weekly dosing was needed in 16.4%. Parallel azathioprine therapy and clinical remission at week 12 was inversely associated to dose escalation to weekly dosing.

Conclusion: Clinical efficacy and normalized C-reactive protein at week 12, need for combined immunosuppression, luminal disease and smoking are predictors for medium term clinical efficacy/mucosal healing during adalimumab therapy, while parallel azathioprine therapy may decrease the probability for dose escalation.

Publication types

  • English Abstract
  • Multicenter Study

MeSH terms

  • Adalimumab
  • Adult
  • Anti-Inflammatory Agents / administration & dosage*
  • Anti-Inflammatory Agents / pharmacology*
  • Antibodies, Monoclonal / administration & dosage*
  • Antibodies, Monoclonal / pharmacology*
  • Antibodies, Monoclonal, Humanized
  • Azathioprine / administration & dosage
  • Azathioprine / pharmacology
  • Biomarkers / blood
  • C-Reactive Protein / metabolism
  • Crohn Disease / complications
  • Crohn Disease / drug therapy*
  • Crohn Disease / pathology
  • Crohn Disease / physiopathology
  • Female
  • Follow-Up Studies
  • Humans
  • Hungary
  • Immunosuppressive Agents / administration & dosage
  • Immunosuppressive Agents / pharmacology
  • Intestinal Fistula / etiology*
  • Intestinal Mucosa / drug effects*
  • Kaplan-Meier Estimate
  • Logistic Models
  • Male
  • Odds Ratio
  • Predictive Value of Tests
  • Recurrence
  • Smoking / adverse effects
  • Time Factors
  • Treatment Outcome
  • Wound Healing / drug effects*

Substances

  • Anti-Inflammatory Agents
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Biomarkers
  • Immunosuppressive Agents
  • C-Reactive Protein
  • Adalimumab
  • Azathioprine