Durability of Adalimumab and Infliximab in Children With Crohn’s Disease: A Nationwide Comparison From the epi-IIRN Cohort

Author:

Atia Ohad1ORCID,Friss Chagit1,Focht Gili1,Magen Rimon Ramit2,Ledderman Natan3,Ben-Tov Amir45,Loewenberg Weisband Yiska6,Matz Eran7,Gorelik Yuri8,Chowers Yehuda8,Dotan Iris95,Turner Dan1

Affiliation:

1. Juliet Keidan Institute of Pediatric Gastroenterology Hepatology and Nutrition, Shaare Zedek Medical Center, The Hebrew University of Jerusalem , Israel

2. Pediatric Gastroenterology & Nutrition institute, Ruth Rappaport Children’s Hospital, Rambam Medical Center, Faculty of Medicine , Technion, Haifa , Israel

3. Meuhedet Health Services , Tel-Aviv , Israel

4. Kahn Sagol Maccabi Research and Innovation Center, Maccabi Healthcare Services , Tel-Aviv , Israel

5. The Faculty of Medicine, Tel Aviv University , Israel

6. Clalit Health Services, Clalit Research Institute , Tel-Aviv , Israel

7. Leumit Health Services , Tel-Aviv , Israel

8. Technion Israel Institute of Technology, Department of Gastroenterology, Rambam Healthcare Campus, Bruce Rappaport School of Medicine , Haifa , Israel

9. Division of Gastroenterology, Rabin Medical Center , Petah Tikva , Israel

Abstract

Abstract Background In a nationwide cohort, we aimed to compare the durability of infliximab and adalimumab as first biologic treatment in children with Crohn’s disease (CD), stratified as combotherapy or monotherapy. Methods We used data from the epi-IIRN cohort that includes all patients with inflammatory bowel diseases in Israel. Durability was defined as consistent treatment without surgery or treatment escalation. All comparisons followed stringent propensity-score matching in Cox proportional hazard models. Results Of the 3487 children diagnosed with CD since 2005, 2157 (62%) received biologics (1127 [52%] infliximab, 964 [45%] adalimumab and 52 [2%] vedolizumab as first biologic), representing a higher proportion than that among adults diagnosed during the same time period (5295 of 15 776 [34%]; P < .001). Time from diagnosis to initiation of biologic was shorter in pediatric-onset compared with adult-onset disease (median time during the last 3 years was 2.7 months [interquartile range 1.2-5.4] vs 5.2 months [2.6-8.9]; P < .001). The durability of adalimumab monotherapy after 1 and 5 years from initiation of treatment was better than infliximab monotherapy (79%/54% vs 67%/37%, respectively; n = 452 matched children; hazard ratio [HR], 1.7; 95% confidence interval [CI], 1.3-2.3; P < .001), while in those treated with combotherapy, durability was similar (94%/66% with infliximab vs 90%/54% with adalimumab; n = 100; HR, 1.7; 95% CI, 0.9-3.3; P = .1). Durability was higher in children treated with infliximab combotherapy vs infliximab monotherapy (87%/45% vs 75%/39%; n = 440; HR, 1.4; 95% CI, 1.1-1.8; P = .01). The durability of adalimumab monotherapy was similar to infliximab combotherapy (83%/53% vs 89%/56%, respectively; n = 238; HR, 0.9; 95% CI, 0.7-1.2; P = .4). Conclusion Our results support using adalimumab monotherapy as a first-line biologic in children with CD. When infliximab is used, combotherapy may be advantageous over monotherapy.

Funder

Leona M. and Harry B. Helmsley Charitable Trust

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

Reference40 articles.

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