Evidence map›Paper›PMID 32813123›Full record

ArticleEuropean journal of pediatrics2020

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

Maria M E Jongsma, Dwight A Winter, Hien Q Huynh, Lorenzo Norsa, Seamus Hussey, Kaija-Leena Kolho, Jiri Bronsky, Amit Assa, Shlomi Cohen, Raffi Lev-Tzion and 9 more

Abstract read
In one paragraph

Article in European journal of pediatrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 5 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 5 syntheses or guidelines pooled it.

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  13. [Research progress on biologics and therapeutic drug monitoring in pediatric inflammatory bowel disease].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Maria M E JongsmaDepartment of Paediatric Gastroenterology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.
Dwight A WinterDepartment of Paediatric Gastroenterology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.
Hien Q HuynhDivision of Paediatric Gastroenterology and Nutrition, Edmonton Paediatric IBD Clinic (EPIC), University of Alberta, Edmonton, Canada.
Lorenzo NorsaDepartment of Paediatric Gastroenterology Hepatology and Nutrition, Hôpital Necker-Enfants-Malades, Paris, France.
Seamus HusseyDepartment of Paediatric Gastroenterology, Our Lady's Children's Hospital and RCSI, Dublin, Ireland.
Kaija-Leena KolhoDepartment of Paediatric Gastroenterology, Tampere University Hospital and University of Tampere, Tampere, Finland and Children's Hospital, University of Helsinki, Helsinki, Finland.
Jiri BronskyDepartment of Paediatrics, Gastroenterology and Nutrition Unit, University Hospital Motol, Prague, Czech Republic.
Amit AssaInstitute of Paediatric Gastroenterology, Schneider Children's Hospital, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Shlomi CohenPaediatric Gastroenterology unit, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center and the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Raffi Lev-TzionDepartment of Paediatric Gastroenterology, Shaare Zedek Medical Center, Jerusalem, Israel.
Stephanie Van BiervlietDepartment of Paediatric Gastroenterology, Universitair Ziekenhuis, Ghent, Belgium.
Dimitris RizopoulosDepartment of Biostatistics, Erasmus Medical Center, Rotterdam, The Netherlands.
Tim G J de MeijDepartment of Paediatric Gastroenterology, Amsterdam UMC - Vrije Universiteit/Emma Children's Hospital, Amsterdam, The Netherlands.
Dror S ShouvalPaediatric 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.
Eytan WineDivision of Paediatric Gastroenterology and Nutrition, Edmonton Paediatric IBD Clinic (EPIC), University of Alberta, Edmonton, Canada.
Victorien M WoltersDepartment of Paediatric Gastroenterology, Utrecht Medical Center/Wilhelmina Children's Hospital, Utrecht, The Netherlands.
Christine Martinez-VinsonDepartment of Paediatric Gastroenterology, Hôpital Robert Debré, Paris, France.
Lissy de RidderDepartment of Paediatric Gastroenterology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands. l.deridder@erasmusmc.nl.
Paediatric IBD Porto Group of ESPGHAN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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).

Indexed as

Gastrointestinal AgentsInflammatory Bowel DiseasesInfliximabChildChild, PreschoolFemaleHumansMaleRetrospective StudiesGastrointestinal AgentsInfliximabAnti-TNFBiologicsClinical pharmacologyCrohn’s diseaseGastroenterologyPaediatricUlcerative colitis

Identifiers

PMID32813123
PMCPMC7666662

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.