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.

biologics early treatment inflammatory bowel disease risk-stratification

Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
27 Nov 2023
Historique:
received: 05 09 2023
medline: 28 11 2023
pubmed: 28 11 2023
entrez: 27 11 2023
Statut: aheadofprint

Résumé

Treatment guidelines for paediatric Crohn's disease (CD) suggest early use of anti-tumour necrosis factor alpha (anti-TNF) in high-risk individuals. The aim is to evaluate the effect of early anti-TNF in a real-world cohort. Children 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. In 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 to 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 to no POPO (5.05 [95%CI 2.45-10.43] vs. 3.41 [95%CI 0.54-21.7]). In this cohort of children with newly-diagnosed CD, early anti-TNF demonstrated superior effectiveness in high-risk patients.

Sections du résumé

BACKGROUND & AIMS OBJECTIVE
Treatment guidelines for paediatric Crohn's disease (CD) suggest early use of anti-tumour necrosis factor alpha (anti-TNF) in high-risk individuals. The aim is to evaluate the effect of early anti-TNF in a real-world cohort.
METHODS METHODS
Children 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.
RESULTS RESULTS
In 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 to 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 to no POPO (5.05 [95%CI 2.45-10.43] vs. 3.41 [95%CI 0.54-21.7]).
CONCLUSION CONCLUSIONS
In this cohort of children with newly-diagnosed CD, early anti-TNF demonstrated superior effectiveness in high-risk patients.

Identifiants

pubmed: 38011797
pii: 7452723
doi: 10.1093/ecco-jcc/jjad197
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation.

Auteurs

Renz C W Klomberg (RCW)

Department of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.

Hella C van der Wal (HC)

Department of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.

Martine A Aardoom (MA)

Department of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.

Polychronis Kemos (P)

Pediatric Gastroenterology, Centre for Immunobiology, Blizard Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.

Dimitris Rizopoulos (D)

Department of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.

Frank M Ruemmele (FM)

Department of Pediatric Gastroenterology, Université Paris Descartes, Sorbonne Paris Cité, APHP, Hôpital Necker Enfants Malades, Paris, France.

Mohammed Charrout (M)

Delft Bioinformatics Lab, Delft University of Technology, Delft, the Netherlands.

J C Escher (JC)

Department of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.

Nicholas M Croft (NM)

Pediatric Gastroenterology, Centre for Immunobiology, Blizard Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kingdom.

Lissy de Ridder (L)

Department of Pediatric Gastroenterology, Sophia Children's Hospital, Rotterdam, The Netherlands.

Ivan D Milovanovich (ID)

Department of Gastroenterology, Hepatology, and Endoscopy, University Children's Hospital, Belgrade, Serbia.

James J Ashton (JJ)

Department of Paediatric Gastroenterology, Southampton Children's Hospital, Southampton, United Kingdom, Human Genetics and Genomic Medicine, University of Southampton, Southampton, United Kingdom.

Paul Henderson (P)

Department of Paediatric Gastroenterology and Nutrition, Royal Hospital for Children and Young People, Edinburgh, United Kingdom, Child Life and Health, University of Edinburgh, Edinburgh, United Kingdom.

Oren Ledder (O)

Juliet Keidan Institute of Paediatric Gastroenterology and Nutrition, Shaare Zedek Medical Center, Hebrew University of Jerusalem, Jerusalem, Israel.

Tim G J de Meij (TGJ)

Department of Pediatric Gastroenterology, Emma Children's Hospital, Amsterdam UMC, Amsterdam, the Netherlands.

Richard Hansen (R)

Clinical Reader in Child Health, Department of Child Health, Division of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, Scotland, Department of Paediatric Gastroenterology, Royal Hospital for Children, Glasgow, Scotland.

Thalia Z Hummel (TZ)

Department of Paediatric Gastroenterology, Medisch Spectrum Twente, Enschede, the Netherlands.

Katsuhiro Arai (K)

Division of Gastroenterology, National Center for Child Health and Development, Tokyo, Japan.

Astor Rodrigues (A)

Department of Paediatric Gastroenterology, Oxford Children's Hospital, Oxford, United Kingdom.

Fiona Cameron (F)

Department of Pediatric Gastroenterology, Hepatology and Nutrition, Alder Hey Children's NHS Foundation Trust, Liverpool, United Kingdom.

Sibylle Koletzko (S)

Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, LMU Munich, Munich, Germany, Department of Pediatrics, Gastroenterology and Nutrition, School of Medicine Collegium Medicum University of Warmia and Mazury, Olsztyn, Poland.

Rafeeq Muhammed (R)

Department of Paediatric Gastroenterology, Birmingham Children's Hospital, Birmingham, United Kingdom.

Natalia Nedelkopoulou (N)

Department of Paediatric Gastroenterology, Sheffield Children's Hospital, Sheffield, United Kingdom.

Classifications MeSH