Evidence map›Paper›PMID 38011797›Full record

Observational studyJournal of Crohn's & colitis2024

Improved Clinical Outcomes With Early Anti-Tumour Necrosis Factor Alpha Therapy in Children With Newly Diagnosed Crohn's Disease: Real-world Data from the International Prospective PIBD-SETQuality Inception Cohort Study.

Renz C W Klomberg, Hella C van der Wal, Martine A Aardoom, Polychronis Kemos, Dimitris Rizopoulos, Frank M Ruemmele, Mohammed Charrout, Hankje C Escher, Nicholas M Croft, Lissy de Ridder and 1 more

Open access · hybridAbstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Journal of Crohn's & colitis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% of its field
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Observational
  5. [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
    Review
  6. Article
  7. Review
  8. Article
  9. Article
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

11 authors at 15 institutions in 8 countries.

Renz C W KlombergDepartment of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.ORCID 0000-0002-7736-0704
Hella C van der WalDepartment of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.
Martine A AardoomDepartment of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.
Polychronis KemosPediatric Gastroenterology, Centre for Immunobiology, Blizard Institute, Barts and the London School of Medicine, Queen Mary University of London, London, UK.
Dimitris RizopoulosDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0001-9397-0900
Frank M RuemmeleDepartment of Pediatric Gastroenterology, Université Paris Descartes, Sorbonne Paris Cité, Hôpital Necker Enfants Malades, Paris, France.
Mohammed CharroutDelft Bioinformatics Laboratory, Delft University of Technology, Delft, The Netherlands.ORCID 0000-0002-3405-1995
Hankje C EscherDepartment of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.
Nicholas M CroftPediatric Gastroenterology, Centre for Immunobiology, Blizard Institute, Barts and the London School of Medicine, Queen Mary University of London, London, UK.ORCID 0000-0002-1519-6435
Lissy de RidderDepartment of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.
PIBD-SETQuality collaborative group
Erasmus MC - Sophia Children’s Hospital · NLAlder Hey Children's NHS Foundation Trust · GBBirmingham Children's Hospital · GBHebrew University of Jerusalem · ILQueen Mary University of London · GBUniversity of Dundee · GBDelft University of Technology · NLErasmus University Rotterdam · NLHôpital Necker-Enfants Malades · FRMedisch Spectrum Twente · NLNational Center For Child Health and Development · JPRoyal Hospital for Children · GBSheffield Children's Hospital · GBSouthampton Children's Hospital · GBUniversity Children's Hospital, Belgrade · RS

Funding

European Union's Horizon 668023
6 · The paper itself

Abstract

BACKGROUND AND

aimsTreatment guidelines for paediatric Crohn's disease [CD] suggest early use of anti-tumour necrosis factor alpha [anti-TNFα] in high-risk individuals. The aim is to evaluate the effect of early anti-TNF in a real-world cohort.

methodsChildren with newly diagnosed CD were prospectively recruited at 28 participating sites of the international observational PIBD-SETQuality study. Outcomes were compared at 3 months, 1 and 2 years between patients receiving early anti-TNF [<90 days after diagnosis] and those not receiving early anti-TNF. Outcomes included sustained steroid-free remission [SSFR] without treatment intensification [specified as SSFR*] and sustained steroid-free mild/inactive disease without treatment intensification [specified as SSFMI*]. Penalised logistic regression model-based standardisation was applied to estimate the relative risks [RR] of early therapy on outcomes. RRs were estimated for high-risk and low-risk patients, based on presence of predictors of poor outcome [POPOs] and disease activity at diagnosis.

resultsIn total, 331 children (median age 13.9 years [IQR 12.2-15.3]) were enrolled, with 135 [41%] receiving early anti-TNF. At 1 year, patients on early anti-TNF had higher rates of SSFR* [30% vs 14%, p <0.001] and SSFMI* [69% vs 33%, p <0.001], with RRs of 2.95 [95% CI 1.63-5.36] and 4.67 [95% CI 2.46-8.87], respectively. At 1 year, the RRs for SSFMI* were higher, and statistically significant in high-risk patients, i.e. those with moderate/severe disease compared with mild/inactive disease at diagnosis (5.50 [95% CI 2.51-12.05] vs 2.91 [95% CI 0.92-9.11]), and those with any POPO compared with no POPO (5.05 [95% CI 2.45-10.43] vs 3.41 [95% CI 0.54-21.7]).

conclusionIn this cohort of children with newly-diagnosed CD, early anti-TNF demonstrated superior effectiveness in high-risk patients.

Indexed as

Crohn DiseaseTumor Necrosis Factor-alphaAdalimumabAdolescentChildChild, PreschoolFemaleGastrointestinal AgentsHumansInfliximabMaleProspective StudiesRemission InductionSeverity of Illness IndexTreatment OutcomeAdalimumabGastrointestinal AgentsInfliximabTumor Necrosis Factor-alphaBiologicsearly treatmentinflammatory bowel diseaserisk-stratification

Identifiers

PMID38011797
PMCPMC11140629
OpenAlexW4389099356

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.