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      Infliximab in young paediatric IBD patients: it is all about the dosing

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          Abstract

          Infliximab (IFX) is administered intravenously using weight-based dosing (5 mg/kg) in inflammatory bowel disease (IBD) patients. Our hypothesis is that especially young children need a more intensive treatment regimen than the current weight-based dose administration. We aimed to assess IFX pharmacokinetics (PK), based on existing therapeutic drug monitoring (TDM) data in IBD patients < 10 years. TDM data were collected retrospectively in 14 centres. Children treated with IFX were included if IFX was started as IBD treatment at age < 10 years (young patients, YP) and PK data were available. Older IBD patients aged 10–18 years were used as controls (older patients, OP). Two hundred and fifteen paediatric inflammatory bowel disease (PIBD) patients were eligible for the study (110 < 10 year; 105 ≥ 10 years). Median age was 8.3 years (IQR 6.9–8.9) in YP compared with 14.3 years (IQR 12.8–15.6) in OP at the start of IFX. At the start of maintenance treatment, 72% of YP had trough levels below therapeutic range (< 5.4 μg/mL). After 1 year of scheduled IFX maintenance treatment, YP required a significantly higher dose per 8 weeks compared with OP (YP; 9.0 mg/kg (IQR 5.0–12.9) vs. OP; 5.5 mg/kg (IQR 5.0–9.3); p < 0.001). The chance to develop antibodies to infliximab was relatively lower in OP than YP (0.329 (95% CI − 1.2 to − 1.01); p < 0.001), while the overall duration of response to IFX was not significantly different (after 2 years 53% ( n = 29) in YP vs. 58% ( n = 45) in OP; p = 0.56).

          Conclusion: Intensification of the induction scheme is suggested for PIBD patients aged < 10 years.

          What is Known?

          •Infliximab trough levels of paediatric IBD patients are influenced by several factors as dosing scheme, antibodies and inflammatory markers.

          •In 4.5–30% of the paediatric IBD patients, infliximab treatment was stopped within the first year.

          What is New?

          •The majority of young PIBD (< 10 years) have inadequate IFX trough levels at the start of maintenance treatment.

          •Young PIBD patients (< 10 years) were in need of a more intensive treatment regimen compared with older paediatric patients during 1 year of IFX treatment.

          •The chance to develop antibodies to infliximab was relatively higher in young PIBD patients (< 10 years).

          Electronic supplementary material

          The online version of this article (10.1007/s00431-020-03750-0) contains supplementary material, which is available to authorized users.

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          Most cited references32

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          Infliximab, azathioprine, or combination therapy for Crohn's disease.

          The comparative efficacy and safety of infliximab and azathioprine therapy alone or in combination for Crohn's disease are unknown. In this randomized, double-blind trial, we evaluated the efficacy of infliximab monotherapy, azathioprine monotherapy, and the two drugs combined in 508 adults with moderate-to-severe Crohn's disease who had not undergone previous immunosuppressive or biologic therapy. Patients were randomly assigned to receive an intravenous infusion of 5 mg of infliximab per kilogram of body weight at weeks 0, 2, and 6 and then every 8 weeks plus daily oral placebo capsules; 2.5 mg of oral azathioprine per kilogram daily plus a placebo infusion on the standard schedule; or combination therapy with the two drugs. Patients received study medication through week 30 and could continue in a blinded study extension through week 50. Of the 169 patients receiving combination therapy, 96 (56.8%) were in corticosteroid-free clinical remission at week 26 (the primary end point), as compared with 75 of 169 patients (44.4%) receiving infliximab alone (P=0.02) and 51 of 170 patients (30.0%) receiving azathioprine alone (P<0.001 for the comparison with combination therapy and P=0.006 for the comparison with infliximab). Similar numerical trends were found at week 50. At week 26, mucosal healing had occurred in 47 of 107 patients (43.9%) receiving combination therapy, as compared with 28 of 93 patients (30.1%) receiving infliximab (P=0.06) and 18 of 109 patients (16.5%) receiving azathioprine (P<0.001 for the comparison with combination therapy and P=0.02 for the comparison with infliximab). Serious infections developed in 3.9% of patients in the combination-therapy group, 4.9% of those in the infliximab group, and 5.6% of those in the azathioprine group. Patients with moderate-to-severe Crohn's disease who were treated with infliximab plus azathioprine or infliximab monotherapy were more likely to have a corticosteroid-free clinical remission than those receiving azathioprine monotherapy. (ClinicalTrials.gov number, NCT00094458.) 2010 Massachusetts Medical Society
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            Pediatric modification of the Montreal classification for inflammatory bowel disease: the Paris classification.

            Crohn's disease and ulcerative colitis are complex disorders with some shared and many unique predisposing genes. Accurate phenotype classification is essential in determining the utility of genotype-phenotype correlation. The Montreal Classification of IBD has several weaknesses with respect to classification of children. The dynamic features of pediatric disease phenotype (change in disease location and behavior over time, growth failure) are not sufficiently captured by the current Montreal Classification. Focusing on facilitating research in pediatric inflammatory bowel disease (IBD), and creating uniform standards for defining IBD phenotypes, an international group of pediatric IBD experts met in Paris, France to develop evidence-based consensus recommendations for a pediatric modification of the Montreal criteria. Important modifications developed include classifying age at diagnosis as A1a (0 to 40 years), distinguishing disease above the distal ileum as L4a (proximal to ligament of Treitz) and L4b (ligament of Treitz to above distal ileum), allowing both stenosing and penetrating disease to be classified in the same patient (B2B3), denoting the presence of growth failure in the patient at any time as G(1) versus G(0) (never growth failure), adding E4 to denote extent of ulcerative colitis that is proximal to the hepatic flexure, and denoting ever severe ulcerative colitis during disease course by S1. These modifications are termed the Paris Classification. By adhering to the Montreal framework, we have not jeopardized or altered the ability to use this classification for adult onset disease or by adult gastroenterologists. Copyright © 2010 Crohn's & Colitis Foundation of America, Inc.
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              • Article: not found

              Induction and maintenance infliximab therapy for the treatment of moderate-to-severe Crohn's disease in children.

              The REACH study evaluated the safety and efficacy of infliximab in children with moderately to severely active Crohn's disease. Patients (n = 112) with a Pediatric Crohn's Disease Activity Index (PCDAI) score >30 received infliximab 5 mg/kg at weeks 0, 2, and 6. Patients responding to treatment at week 10 were randomized to infliximab 5 mg/kg every 8 or 12 weeks through week 46. A concurrent immunomodulator was required. Clinical response (decrease from baseline in the PCDAI score > or =15 points; total score < or =30) and clinical remission (PCDAI score < or =10 points) were evaluated at weeks 10, 30, and 54. At week 10, 99 of 112 (88.4%) patients responded to infliximab (95% confidence interval: [82.5%, 94.3%]) and 66 of 112 (58.9%) patients achieved clinical remission (95% confidence interval: [49.8%, 68.0%]). At week 54, 33 of 52 (63.5%) and 29 of 52 (55.8%) patients receiving infliximab every 8 weeks did not require dose adjustment and were in clinical response and clinical remission, respectively, compared with 17 of 51 (33.3%) and 12 of 51 (23.5%) patients receiving treatment every 12 weeks (P = .002 and P < .001, respectively). Pediatric patients responding to an induction regimen of infliximab were more likely to be in clinical response and remission at week 54 without dose adjustment when their maintenance therapy was given every 8 weeks rather than every 12 weeks. Allowing for dose intensification in the case of relapse, remission rates, but not response rates, at week 54 were superior with every 8-week dosing compared with every 12-week dosing.
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                Author and article information

                Contributors
                m.jongsma@erasmusmc.nl
                d.winter@cjgrijnmond.nl
                Hien.Huynh@ualberta.ca
                lonorsa@hotmail.com
                seamus.hussey@ucd.ie
                kaija-leena.kolho@helsinki.fi
                jiri.bronsky@gmail.com
                amitas@clalit.org.il
                shlomico@tlvmc.gov.il
                raffilv@szmc.org.il
                Stephanie.VanBiervliet@uzgent.be
                d.rizopoulos@erasmusmc.nl
                t.demeij@amsterdamumc.nl
                Dror.shouval@gmail.com
                wine@ualberta.ca
                v.m.wolters@umcutrecht.nl
                christine.martinez-vinson@aphp.fr
                l.deridder@erasmusmc.nl
                Journal
                Eur J Pediatr
                Eur J Pediatr
                European Journal of Pediatrics
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0340-6199
                1432-1076
                19 August 2020
                19 August 2020
                2020
                : 179
                : 12
                : 1935-1944
                Affiliations
                [1 ]GRID grid.416135.4, Department of Paediatric Gastroenterology, , Erasmus Medical Center/Sophia Children’s Hospital, ; Rotterdam, The Netherlands
                [2 ]GRID grid.17089.37, Division of Paediatric Gastroenterology and Nutrition, Edmonton Paediatric IBD Clinic (EPIC), , University of Alberta, ; Edmonton, Canada
                [3 ]GRID grid.412134.1, ISNI 0000 0004 0593 9113, Department of Paediatric Gastroenterology Hepatology and Nutrition, , Hôpital Necker-Enfants-Malades, ; Paris, France
                [4 ]GRID grid.417322.1, ISNI 0000 0004 0516 3853, Department of Paediatric Gastroenterology, , Our Lady’s Children’s Hospital and RCSI, ; Dublin, Ireland
                [5 ]GRID grid.7737.4, ISNI 0000 0004 0410 2071, Department of Paediatric Gastroenterology, Tampere University Hospital and University of Tampere, Tampere, Finland and Children’s Hospital, , University of Helsinki, ; Helsinki, Finland
                [6 ]GRID grid.412826.b, ISNI 0000 0004 0611 0905, Department of Paediatrics, Gastroenterology and Nutrition Unit, , University Hospital Motol, ; Prague, Czech Republic
                [7 ]GRID grid.12136.37, ISNI 0000 0004 1937 0546, Institute of Paediatric Gastroenterology, Schneider Children’s Hospital, affiliated to the Sackler Faculty of Medicine, , Tel Aviv University, ; Tel Aviv, Israel
                [8 ]GRID grid.12136.37, ISNI 0000 0004 1937 0546, Paediatric Gastroenterology unit, Dana-Dwek Children’s Hospital, Tel Aviv Sourasky Medical Center and the Sackler Faculty of Medicine, , Tel Aviv University, ; Tel Aviv, Israel
                [9 ]GRID grid.415593.f, ISNI 0000 0004 0470 7791, Department of Paediatric Gastroenterology, , Shaare Zedek Medical Center, ; Jerusalem, Israel
                [10 ]GRID grid.410566.0, ISNI 0000 0004 0626 3303, Department of Paediatric Gastroenterology, , Universitair Ziekenhuis, ; Ghent, Belgium
                [11 ]GRID grid.5645.2, ISNI 000000040459992X, Department of Biostatistics, , Erasmus Medical Center, ; Rotterdam, The Netherlands
                [12 ]Department of Paediatric Gastroenterology, Amsterdam UMC - Vrije Universiteit/Emma Children’s Hospital, Amsterdam, The Netherlands
                [13 ]GRID grid.12136.37, ISNI 0000 0004 1937 0546, Paediatric Gastroenterology Unit, Edmond and Lily Safra Children’s Hospital Sheba Medical Center, Ramat Gan, and Sackler Faculty of Medicine, , Tel Aviv University, ; Tel Aviv, Israel
                [14 ]Department of Paediatric Gastroenterology, Utrecht Medical Center/Wilhelmina Children’s Hospital, Utrecht, The Netherlands
                [15 ]GRID grid.413235.2, ISNI 0000 0004 1937 0589, Department of Paediatric Gastroenterology, , Hôpital Robert Debré, ; Paris, France
                Author notes

                Communicated by Peter de Winter

                Article
                3750
                10.1007/s00431-020-03750-0
                7666662
                32813123
                66da5b94-1b0e-49fc-a380-6c406506495c
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 13 April 2020
                : 16 July 2020
                : 21 July 2020
                Funding
                Funded by: University Medical Center Rotterdam (Erasmus MC)
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2020

                Pediatrics
                crohn’s disease,ulcerative colitis,anti-tnf,clinical pharmacology,paediatric,gastroenterology,biologics

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