Trough serum infliximab: a predictive factor of clinical outcome for infliximab treatment in acute ulcerative colitis
| Autor: | A H Steinhart, Cynthia H. Seow, Sandra Irwin, Gordon R. Greenberg, Mark S. Silverberg, A Newman |
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| Rok vydání: | 2009 |
| Předmět: |
Adult
Male musculoskeletal diseases medicine.medical_specialty Adolescent medicine.medical_treatment Colonoscopy Lower risk Risk Assessment Gastroenterology Drug Administration Schedule Cohort Studies Young Adult Gastrointestinal Agents immune system diseases Internal medicine Humans Medicine Colitis skin and connective tissue diseases Colectomy Aged Gastrointestinal agent medicine.diagnostic_test business.industry Remission Induction Antibodies Monoclonal Middle Aged Prognosis medicine.disease Ulcerative colitis Infliximab Surgery stomatognathic diseases Treatment Outcome Acute Disease Antibody Formation Cohort Colitis Ulcerative Female Drug Monitoring business medicine.drug |
| Zdroj: | Gut. 59:49-54 |
| ISSN: | 0017-5749 |
| Popis: | Antibodies to infliximab reduce serum infliximab with loss of clinical benefit, but undetectable trough serum concentrations of infliximab may occur without antibody formation. The relationship between trough serum infliximab and clinical outcomes was evaluated in acute ulcerative colitis.In a cohort of 115 patients with ulcerative colitis treated with three-dose induction followed by scheduled maintenance infliximab, rates of clinical remission, colectomy, antibodies to infliximab and trough serum infliximab were determined.Rates of remission were 32% at week 10 and 37% at week 54. Colectomy occurred in 40% of patients, at a median of 5.3 (IQR 1.9-12.1) months. Detectable trough serum infliximab was present in 39% of patients and, among patients with undetectable infliximab, 41% were antibody positive and 20% were antibody negative. For antibody-positive and antibody-negative patients, rates of remission (18% vs 14%), endoscopic improvement (25% vs 35%) and colectomy (52% vs 59%) were not different. A detectable serum infliximab was associated with higher rates of remission (69% vs 15%; p0.001) and endoscopic improvement (76% vs 28%, p0.001). An undetectable serum infliximab predicted an increased risk for colectomy (55% vs 7%, OR 9.3; 95% CI 2.9 to 29.9; p0.001). Concurrent immunosuppression was not associated with clinical outcomes.For patients with ulcerative colitis treated with infliximab, a detectable trough serum infliximab predicts clinical remission, endoscopic improvement and a lower risk for colectomy. An undetectable trough serum infliximab, irrespective of antibody status, is associated with less favourable outcomes. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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