A Treat-to-Target Strategy Guided by Pan-Enteric Evaluation in Children With Crohn’s Disease Improves Outcomes at 2 Years

Author:

D’Arcangelo Giulia1,Russo Giusy1,Aloi Marina1,Ruggiero Cosimo1,Maccioni Francesca2,Hassan Cesare34,Papoff Paola5,Cohen Stanley Allen6,Oliva Salvatore1ORCID

Affiliation:

1. Pediatric Gastroenterology and Liver Unit, Maternal and Child Health Department, Sapienza University of Rome , Rome , Italy

2. Department of Radiological Sciences, Oncology, and Pathology, Sapienza University of Rome , Rome , Italy

3. Department of Gastroenterology, IRCCS Humanitas Research Hospital , Rozzano , Italy

4. Department of Biomedical Sciences, Humanitas University , Pieve Emanuele , Italy

5. Pediatric Intensive Care Unit, Maternal and Child Health Department, Sapienza University of Rome , Rome , Italy

6. Children’s Center for Digestive Health Care, Children’s Healthcare of Atlanta, and Emory University , Atlanta, Georgia , United States

Abstract

Abstract Background and Aims It is uncertain whether a treat-to-target approach could be an effective strategy for improving outcomes in children with Crohn’s disease (CD). Previously, we reported mucosal healing (MH) and deep remission rates throughout the intestinal tract by performing 3 pan-enteric capsule assessments and using a treat-to-target strategy over 52 weeks in children with CD. This report describes the outcomes of this approach at 104 weeks. Methods Children with known CD who completed the 52-week protocol repeated pan-enteric capsule endoscopy (PCE) at 104 weeks. Results at weeks 52 and 104 were compared, and long-term outcomes between patients, with and without MH, were calculated using an intention-to-treat analysis of clinical relapse, need for steroids, treatment escalation, hospitalization, and surgery. Results Of the previous study cohort of 48 patients, 46 (96%) were available for this extension study (28 [61%] of 46 with MH and 18 [39%] of 46 without MH at 52 weeks). When evaluated at 104 weeks, MH was maintained in 93% of patients with MH at 52 weeks. In the intention-to-treat analysis, complete MH at 52 weeks was associated with reduced risk of steroid use (log-rank P < .0001), treatment escalation (log-rank P < .0001), hospitalization (log-rank P < .0001), and clinical relapse (log-rank P < .0001). Conclusions When a PCE-based, treat-to-target strategy is employed, MH is sustainable (93%) over a 1-year period and is correlated with improved patient outcomes, including reduced need for steroids, treatment escalation, hospitalization, and clinical relapses at 104 weeks. ClinicalTrials.gov number: NCT03161886.

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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