Success and safety of high infliximab trough levels in inflammatory bowel disease

Scand J Gastroenterol. 2018 Aug;53(8):940-946. doi: 10.1080/00365521.2018.1486882. Epub 2018 Jul 10.

Abstract

Objective: A prospective trial suggests target infliximab trough levels of 3-7 μg/mL, yet data on additional therapeutic benefits and safety of higher trough levels are scarce.

Aim: To explore whether high infliximab trough levels (≥7 μg/mL) are more effective and still safe.

Material and methods: In this cohort study of 183 patients (109 Crohn's disease and 74 ulcerative colitis) on infliximab maintenance treatment at a tertiary referral center we correlated fecal calprotectin and C-reactive protein to trough levels (426 samples) at different time points during treatment. Rates of infections were compared in quadrimesters (four-month periods) with high trough levels to quadrimesters with trough levels <7 μg/mL during 420 patient-years.

Results: Fecal calprotectin and C-reactive protein (median [interquartile range]) were lower in patients with high trough levels (fecal calprotectin 66 mg/kg [30-257]; C-reactive protein 3 mg/L [3-3]) compared to trough levels below 7 μg/mL (fecal calprotectin 155 mg/kg [72-474]; C-reactive protein 3 mg/L [3-14.5]) (p < .001). High trough levels were superior also after excluding samples with trough levels <3 μg/mL from analysis. No differences in rates of infections were observed in quadrimesters with high trough levels (16/129 [12.4%]) compared to quadrimesters with trough levels <7 μg/mL (32/344 [9.3%]) (p = .32). Maintaining high trough levels resulted in 32% (interquartile range: 2-54%) increase of infliximab consumption.

Conclusion: High infliximab trough levels provide better control of inflammation in inflammatory bowel disease without increasing the risk of infection.

Keywords: Therapeutic drug monitoring; combination treatment; cost-effectiveness; infliximab-induced skin manifestations; switch.

MeSH terms

  • Adolescent
  • Adult
  • Biomarkers / analysis*
  • C-Reactive Protein / analysis
  • Cost-Benefit Analysis
  • Drug Monitoring / methods*
  • Feces / chemistry
  • Female
  • Humans
  • Inflammatory Bowel Diseases / drug therapy*
  • Infliximab / administration & dosage*
  • Infliximab / pharmacokinetics
  • Leukocyte L1 Antigen Complex / analysis
  • Logistic Models
  • Male
  • Multivariate Analysis
  • Prospective Studies
  • Remission Induction
  • Slovenia
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Young Adult

Substances

  • Biomarkers
  • Leukocyte L1 Antigen Complex
  • Tumor Necrosis Factor-alpha
  • C-Reactive Protein
  • Infliximab