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Review article: applying pharmacokinetics to optimise dosing of anti-TNF biologics in acute severe ulcerative colitis

期刊

ALIMENTARY PHARMACOLOGY & THERAPEUTICS
卷 41, 期 11, 页码 1094-1103

出版社

WILEY
DOI: 10.1111/apt.13175

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资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health [K23DK09483]
  2. National Institutes of Health Child Health Research Career Development Award [K12HD028827]

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BackgroundAcute severe ulcerative colitis (ASUC), the most aggressive presentation of ulcerative colitis (UC), occurs in 15% of adults and children with UC. First line therapy with intravenous corticosteroids is ineffective in half of adults and one-third of children. Therapeutic monoclonal antibodies against TNF (anti-TNF therapy) are emerging as a common treatment for ASUC due to their similar efficacy to calcineurin inhibitors and more favourable adverse effect profile. AimTo comprehensively review the evidence for anti-TNF therapy for ASUC in children and adults with regard to outcomes and pharmacokinetics. MethodsPubMed and recent conference proceedings were searched using the terms ulcerative colitis', acute severe ulcerative colitis', anti-TNF', pharmacokinetics' and the generic names of specific anti-TNF agents. ResultsOutcomes after anti-TNF therapy for ASUC remain suboptimal with about one half of children and adults undergoing colectomy. While several randomised controlled trials have demonstrated the efficacy of anti-TNF therapy for ambulatory patients with moderate to severely active UC, patients in these studies were less ill than those with ASUC. Patients with ASUC may exhibit more rapid clearance of anti-TNF biologics due to pharmacokinetic mechanisms influenced by disease severity. ConclusionsConventional weight-based dosing effective in patients with moderately to severely active UC, may not be equally effective in those with acute severe ulcerative colitis. Personalised anti-TNF dosing strategies, which integrate patient factors and early measures of pharmacokinetics and response, hold promise for ensuring sustained drug exposure and maximising early mucosal healing in patients with acute severe ulcerative colitis.

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