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10.1016/j.cgh.2020.02.033

http://scihub22266oqcxt.onion/10.1016/j.cgh.2020.02.033
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32109630!ä!32109630

suck abstract from ncbi


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pmid32109630      Clin+Gastroenterol+Hepatol 2021 ; 19 (1): 111-118.e10
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  • Peak Concentrations of Ustekinumab After Intravenous Induction Therapy Identify Patients With Crohn s Disease Likely to Achieve Endoscopic and Biochemical Remission #MMPMID32109630
  • Hanzel J; Zdovc J; Kurent T; Sever N; Javornik K; Tuta K; Kozelj M; Smrekar N; Novak G; Stabuc B; Dreesen E; Thomas D; Vovk T; Grabnar I; Drobne D
  • Clin Gastroenterol Hepatol 2021[Jan]; 19 (1): 111-118.e10 PMID32109630show ga
  • BACKGROUND & AIMS: Little is known about the relationship between ustekinumab exposure during the first 2 weeks of treatment and outcomes of patients with Crohn's disease (CD). We investigated the relationship between serum concentrations of ustekinumab during the first 2 weeks of treatment and endoscopic and biochemical remission in patients with CD. METHODS: In a prospective observational study, we measured concentrations of ustekinumab in serum samples from 41 consecutive patients who started treatment with ustekinumab (approximately 6 mg/kg, intravenously, then 90 mg every 8 weeks), due to endoscopic markers of active CD, at a single center from October 2017 through January 2019. We measured ustekinumab exposure parameters during the first 2 weeks (peak concentration measured immediately after intravenous infusion, week 2 concentration, and area under the curve through week 2). We investigated the correlation between these parameters and endoscopic remission (simple endoscopic score for CD scores of 3 or less without ulceration, assessed centrally) and biochemical remission (level of fecal calprotectin below 100 mg/kg) using the Mann-Whitney U test. RESULTS: Endoscopic remission was achieved in 10 patients (24.4%) at week 24; biochemical remission was achieved in 17 patients (41.5%) at week 8, 17 patients (41.5%) at week 16, and 21 patients (51.2%) at week 24. Peak concentrations associated with endoscopic remission (area under the receiver operating characteristic curve, 0.717; 95% CI, 0.517-0.916); 6 of 13 patients (46%) with peak concentrations above 105 mug/mL (upper tercile) achieved endoscopic remission, compared with only 1 of 14 patients (7%) with peak concentrations below 88 mug/mL (lower tercile). All exposure parameters during the first 2 weeks were associated with biochemical remission. There was no significant difference between the associations of peak concentrations, week-2 concentrations, area under the curve through week 2, or later exposure measures (at weeks 4 and 8) with biochemical or endoscopic remission. CONCLUSIONS: In a prospective study, we found that serum concentrations of ustekinumab as early as 1 hour after intravenous infusion might be used to identify patients with CD most likely to achieve endoscopic remission. This early measurement might be used to optimize treatment of CD.
  • |*Crohn Disease/drug therapy[MESH]
  • |*Ustekinumab/therapeutic use[MESH]
  • |Humans[MESH]
  • |Induction Chemotherapy[MESH]
  • |Prospective Studies[MESH]
  • |Remission Induction[MESH]


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