Optimization of infliximab therapy in inflammatory bowel disease using a dashboard approach-an Indian experience

被引:10
作者
Dave, Mihika B. [1 ]
Dherai, Alpa J. [1 ]
Desai, Devendra C. [2 ]
Mould, Diane R. [3 ]
Ashavaid, Tester F. [1 ]
机构
[1] PD Hinduja Hosp & MRC, Dept Biochem, Veer Savarkar Marg, Mumbai 400016, Maharashtra, India
[2] PD Hinduja Hosp & MRC, Dept Gastroenterol, Veer Savarkar Marg, Mumbai 400016, Maharashtra, India
[3] Project Res Inc, Phoenixville, PA USA
关键词
Inflammatory bowel disease; Infliximab; Antidrug antibody; Therapeutic drug monitoring; Bayesian dashboard; CROHNS-DISEASE; TROUGH LEVELS; PHARMACOKINETICS; BIOLOGICS; ASSOCIATION; MANAGEMENT; ALBUMIN;
D O I
10.1007/s00228-020-02975-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose Infliximab (IFX) therapy in inflammatory bowel disease (IBD) is associated with loss of response in half the patients, due to complex pharmacokinetic and immunological factors. Dashboard's Bayesian algorithms use information from model and individual multivariate determinants of IFX concentration and can predict dose and dosing interval. Aim To compare measured IFX concentrations in our laboratory with values predicted by iDose dashboard system and report its efficacy in managing patients not responding to conventional dosing schedule. Method Clinical history, demographic details, and laboratory findings such as albumin and C-reactive protein (CRP) data of IBD patients (n= 30; median age 23 years (IQR: 14.25 - 33.5)) referred for IFX drug monitoring in our laboratory from November 2017 to November 2019 were entered in iDose software. The IFX concentration predicted by iDose based on this information was compared with that measured in our laboratory. In addition, a prospective dashboard-guided dosing was prescribed in 11 of these 30 patients not responding to conventional dosing and was followed to assess their clinical outcome. Result IFX monitoring in our 30 patients had shown therapeutic concentration in 12, supratherapeutic in 2 and subtherapeutic concentration in 16 patients. The iDose predicted concentration showed concordance in 21 of these 30 patients. Of 11 patients managed with iDose-assisted prospective dosing, 8 achieved clinical remission, 2 showed partial response, and one developed antibodies. Conclusion Retrospective data analysis showed concordance between laboratory measured and iDose-predicted IFX level in 70% of patients. iDose-assisted management achieved clinical remission and cost reduction.
引用
收藏
页码:55 / 62
页数:8
相关论文
共 39 条
  • [31] Shah Swarup A. V., 2018, Drug Metabolism and Personalized Therapy, V33, P57, DOI 10.1515/dmpt-2017-0038
  • [32] EVALUATION OF METHODS FOR ESTIMATING POPULATION PHARMACOKINETIC PARAMETERS .1. MICHAELIS-MENTEN MODEL - ROUTINE CLINICAL PHARMACOKINETIC DATA
    SHEINER, LB
    BEAL, SL
    [J]. JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1980, 8 (06): : 553 - 571
  • [33] Dashboard driven vs. conventional dosing of infliximab in inflammatory bowel disease patients: the PRECISION trial
    Strik, A.
    Berends, S.
    Mould, D.
    Mathot, R.
    Ponsioen, C.
    van den Brande, J.
    Jansen, J.
    Hoekman, D.
    Brandse, J.
    Lowenberg, M.
    D'Haens, G.
    [J]. JOURNAL OF CROHNS & COLITIS, 2019, 13 : S63 - S63
  • [34] Su HY, 2017, TRANSL GASTROENT HEP, V2, DOI 10.21037/tgh.2017.12.05
  • [35] Circulating Interleukin 6 and Albumin, and Infliximab Levels Are Good Predictors of Recovering Efficacy After Dose Escalation Infliximab Therapy in Patients with Loss of Response to Treatment for Crohn's Disease: A Prospective Clinical Trial
    Suzuki, Yasuo
    Matsui, Toshiyuki
    Ito, Hiroaki
    Ashida, Toshifumi
    Nakamura, Shiro
    Motoya, Satoshi
    Matsumoto, Takayuki
    Sato, Noriko
    Ozaki, Kunihiko
    Watanabe, Mamoru
    Hibi, Toshifumi
    [J]. INFLAMMATORY BOWEL DISEASES, 2015, 21 (09) : 2114 - 2122
  • [36] Trough Concentrations of Infliximab Guide Dosing for Patients With Inflammatory Bowel Disease
    Vande Casteele, Niels
    Ferrante, Marc
    Van Assche, Gert
    Ballet, Vera
    Compernolle, Griet
    Van Steen, Kristel
    Simoens, Steven
    Rutgeerts, Paul
    Gils, Ann
    Vermeire, Severine
    [J]. GASTROENTEROLOGY, 2015, 148 (07) : 1320 - +
  • [37] Biologic Concentration Testing in Inflammatory Bowel Disease
    Vaughn, Byron P.
    Sandborn, William J.
    Cheifetz, Adam S.
    [J]. INFLAMMATORY BOWEL DISEASES, 2015, 21 (06) : 1435 - 1442
  • [38] Xu Z, 2012, CLIN PHARM DRUG DEV, V1, P203, DOI DOI 10.1177/2160763X12454673
  • [39] Incidence of suboptimal response to tumor necrosis factor antagonist therapy in inflammatory bowel disease in newly industrialised countries: The EXPLORE study
    Yamamoto-Furusho, Jesus K.
    Al Harbi, Othman
    Armuzzi, Alessandro
    Chan, Webber
    de Leon, Enrique Ponce
    Qian, Jiaming
    Shapina, Marina
    Toruner, Murat
    Tu, Chia-Hung
    Ye, Byong Duk
    Guennec, Morgane
    Sison, Cecilia
    Demuth, Dirk
    Fadeeva, Olga
    Khan, Qasim M. Rana
    [J]. DIGESTIVE AND LIVER DISEASE, 2020, 52 (08) : 869 - 877