Prediction of treatment failure during infliximab induction therapy in inflammatory bowel disease patients based on pharmacokinetic and pharmacodynamic modeling

被引:5
|
作者
Kimura, Koji [1 ]
Yoshida, Atsushi [2 ]
Katagiri, Fumihiko [1 ]
Takayanagi, Risa [1 ]
Yamada, Yasuhiko [1 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Pharm, Dept Clin Evaluat Drug Efficacy, 1432-1 Horinouchi, Hachioji, Tokyo 1920392, Japan
[2] Ofuna Chuo Hosp, Ctr Gastroenterol & Inflammatory Bowel Dis, 6-2-24 Ofuna, Kamakura, Kanagawa 2470056, Japan
关键词
CROHNS-DISEASE; SERUM INFLIXIMAB; 5-AMINOSALICYLIC ACID; RHEUMATOID-ARTHRITIS; MAINTENANCE THERAPY; ULCERATIVE-COLITIS; EFFICACY; ASSOCIATION; ANTIBODIES; REMISSION;
D O I
10.1016/j.ejps.2020.105317
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: In infliximab (IFX) treatment for Crohn's disease (CD) and ulcerative colitis (UC), it is difficult to predict treatment failure during the induction phase. In the present study for optimal IFX treatment, we attempted to estimate serum IFX concentration and clinical response in individual patients during the induction phase to predict the indication of therapeutic effect and the possibility of treatment failure in the maintenance phase. Methods: We estimated pharmacokinetic and pharmacodynamic (PK/PD) parameters and predicted the serum IFX concentration and clinical response using a PK/PD model and Markov chain Monte Carlo Bayesian analysis method during the induction phase. Then, we determined whether the indication of therapeutic effect between predicted and observed clinical response were matched during the maintenance phase. Results: Data obtained from 15 patients were analyzed. The correlation between predicted and observed values of serum IFX concentration (Pearson product-moment correlation coefficient, 0.700; P < 0.0001, n = 68) and clinical response of CD patients (0.790; P < 0.0001, n = 25) and UC patients (0.702; P = 0.0004, n = 21) were significantly high. The indication of therapeutic effect at the final time point of each patient (from day 115 to day 203) were successfully predicted in 14 of 15 patients (93.3%). Conclusions: This study presents prediction of serum IFX concentration and clinical response in individual patients during induction therapy, with presumption of the indication of therapeutic effect and the treatment failure in the maintenance phase. Our results show the possibility of optimizing IFX therapy during the induction phase. © 2020 Elsevier B.V.
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页数:11
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