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Infliximab in young paediatric IBD patients: it is all about the dosing.
Jongsma, Maria M E; Winter, Dwight A; Huynh, Hien Q; Norsa, Lorenzo; Hussey, Seamus; Kolho, Kaija-Leena; Bronsky, Jiri; Assa, Amit; Cohen, Shlomi; Lev-Tzion, Raffi; Van Biervliet, Stephanie; Rizopoulos, Dimitris; de Meij, Tim G J; Shouval, Dror S; Wine, Eytan; Wolters, Victorien M; Martinez-Vinson, Christine; de Ridder, Lissy.
Afiliação
  • Jongsma MME; Department of Paediatric Gastroenterology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Winter DA; Department of Paediatric Gastroenterology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Huynh HQ; Division of Paediatric Gastroenterology and Nutrition, Edmonton Paediatric IBD Clinic (EPIC), University of Alberta, Edmonton, Canada.
  • Norsa L; Department of Paediatric Gastroenterology Hepatology and Nutrition, Hôpital Necker-Enfants-Malades, Paris, France.
  • Hussey S; Department of Paediatric Gastroenterology, Our Lady's Children's Hospital and RCSI, Dublin, Ireland.
  • Kolho KL; Department of Paediatric Gastroenterology, Tampere University Hospital and University of Tampere, Tampere, Finland and Children's Hospital, University of Helsinki, Helsinki, Finland.
  • Bronsky J; Department of Paediatrics, Gastroenterology and Nutrition Unit, University Hospital Motol, Prague, Czech Republic.
  • Assa A; Institute of Paediatric Gastroenterology, Schneider Children's Hospital, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Cohen S; Paediatric Gastroenterology unit, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center and the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Lev-Tzion R; Department of Paediatric Gastroenterology, Shaare Zedek Medical Center, Jerusalem, Israel.
  • Van Biervliet S; Department of Paediatric Gastroenterology, Universitair Ziekenhuis, Ghent, Belgium.
  • Rizopoulos D; Department of Biostatistics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • de Meij TGJ; Department of Paediatric Gastroenterology, Amsterdam UMC - Vrije Universiteit/Emma Children's Hospital, Amsterdam, The Netherlands.
  • Shouval DS; Paediatric Gastroenterology Unit, Edmond and Lily Safra Children's Hospital Sheba Medical Center, Ramat Gan, and Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Wine E; Division of Paediatric Gastroenterology and Nutrition, Edmonton Paediatric IBD Clinic (EPIC), University of Alberta, Edmonton, Canada.
  • Wolters VM; Department of Paediatric Gastroenterology, Utrecht Medical Center/Wilhelmina Children's Hospital, Utrecht, The Netherlands.
  • Martinez-Vinson C; Department of Paediatric Gastroenterology, Hôpital Robert Debré, Paris, France.
  • de Ridder L; Department of Paediatric Gastroenterology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands. l.deridder@erasmusmc.nl.
Eur J Pediatr ; 179(12): 1935-1944, 2020 Dec.
Article em En | MEDLINE | ID: mdl-32813123
ABSTRACT
Infliximab (IFX) is administered intravenously using weight-based dosing (5 mg/kg) in inflammatory bowel disease (IBD) patients. Our hypothesis is that especially young children need a more intensive treatment regimen than the current weight-based dose administration. We aimed to assess IFX pharmacokinetics (PK), based on existing therapeutic drug monitoring (TDM) data in IBD patients < 10 years. TDM data were collected retrospectively in 14 centres. Children treated with IFX were included if IFX was started as IBD treatment at age < 10 years (young patients, YP) and PK data were available. Older IBD patients aged 10-18 years were used as controls (older patients, OP). Two hundred and fifteen paediatric inflammatory bowel disease (PIBD) patients were eligible for the study (110 < 10 year; 105 ≥ 10 years). Median age was 8.3 years (IQR 6.9-8.9) in YP compared with 14.3 years (IQR 12.8-15.6) in OP at the start of IFX. At the start of maintenance treatment, 72% of YP had trough levels below therapeutic range (< 5.4 µg/mL). After 1 year of scheduled IFX maintenance treatment, YP required a significantly higher dose per 8 weeks compared with OP (YP; 9.0 mg/kg (IQR 5.0-12.9) vs. OP; 5.5 mg/kg (IQR 5.0-9.3); p < 0.001). The chance to develop antibodies to infliximab was relatively lower in OP than YP (0.329 (95% CI - 1.2 to - 1.01); p < 0.001), while the overall duration of response to IFX was not significantly different (after 2 years 53% (n = 29) in YP vs. 58% (n = 45) in OP; p = 0.56).

Conclusion:

Intensification of the induction scheme is suggested for PIBD patients aged < 10 years. What is Known? •Infliximab trough levels of paediatric IBD patients are influenced by several factors as dosing scheme, antibodies and inflammatory markers. •In 4.5-30% of the paediatric IBD patients, infliximab treatment was stopped within the first year. What is New? •The majority of young PIBD (< 10 years) have inadequate IFX trough levels at the start of maintenance treatment. •Young PIBD patients (< 10 years) were in need of a more intensive treatment regimen compared with older paediatric patients during 1 year of IFX treatment. •The chance to develop antibodies to infliximab was relatively higher in young PIBD patients (< 10 years).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Doenças Inflamatórias Intestinais / Infliximab Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Gastrointestinais / Doenças Inflamatórias Intestinais / Infliximab Idioma: En Ano de publicação: 2020 Tipo de documento: Article