Volume 71, Issue 4 pp. 516-520
Short Communications: Gastroenterology: Inflammatory Bowel Disease

Therapeutic Drug Monitoring-guided High-dose Infliximab for Infantile-onset Inflammatory Bowel Disease

A Case Series

Amit Assa

Amit Assa

Institute of Gastroenterology, Nutrition and Liver Diseases, Schneider Children's Medical Center, Petach Tikva

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv

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Lev Dorfman

Corresponding Author

Lev Dorfman

Institute of Gastroenterology, Nutrition and Liver Diseases, Schneider Children's Medical Center, Petach Tikva

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv

Address correspondence and reprint requests to Lev Dorfman, MD, Institute of Gastroenterology, Nutrition and Liver Disease, Schneider Children's Medical Center of Israel, 14 Kaplan Street. Petach-Tikva 4920235, Israel (e-mail: [email protected]).Search for more papers by this author
Dror S. Shouval

Dror S. Shouval

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv

Pediatric Gastroenterology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat-Gan

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Raanan Shamir

Raanan Shamir

Institute of Gastroenterology, Nutrition and Liver Diseases, Schneider Children's Medical Center, Petach Tikva

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv

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Shlomi Cohen

Shlomi Cohen

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv

Pediatric Gastroenterology Unit, “Dana-Dwek” Children's Hospital, Tel-Aviv Sourasky Medical Center, Tel Aviv, Israel

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First published: 06 July 2020
Citations: 13

Drs Amit Assa and Lev Dorfman contributed equally to the study and are co-first authors.

The authors report no conflicts of interest.

ABSTRACT

Very early-onset inflammatory bowel disease (IBD) and specifically infantile-onset IBD patients, are characterized by high rates of extensive colonic involvement and decreased response rate to standard therapeutic regimens, including infliximab (IFX). We present a case series of 4 patients with infantile-onset IBD achieving clinical and biologic remission, after treatment with therapeutic drug monitoring (TDM)-guided accelerated high-dose IFX therapy. All patients were treated with accelerated high-dose IFX induction of up to 22 mg/kg. In 3 of these patients, accelerated high-dose IFX was used following failure of intensified standard dose induction. All patients achieved remission following re-induction.

We suggest that children with infantile-onset IBD may require a TDM-guided accelerated high-dose IFX induction and maintenance treatment in order to achieve and maintain remission. Personalized approach in these patients is essential in order to prevent underdosing and to avoid inappropriate interpretation of treatment failure.

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