TY - JOUR
T1 - Infliximab in young paediatric IBD patients
T2 - it is all about the dosing
AU - on behalf of the Paediatric IBD Porto Group of ESPGHAN
AU - Jongsma, Maria M.E.
AU - Winter, Dwight A.
AU - Huynh, Hien Q.
AU - Norsa, Lorenzo
AU - Hussey, Seamus
AU - Kolho, Kaija Leena
AU - Bronsky, Jiri
AU - Assa, Amit
AU - Cohen, Shlomi
AU - Lev-Tzion, Raffi
AU - Van Biervliet, Stephanie
AU - Rizopoulos, Dimitris
AU - de Meij, Tim G.J.
AU - Shouval, Dror S.
AU - Wine, Eytan
AU - Wolters, Victorien M.
AU - Martinez-Vinson, Christine
AU - de Ridder, Lissy
N1 - Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - 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
AB - 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
KW - Anti-TNF
KW - Biologics
KW - Clinical pharmacology
KW - Crohn’s disease
KW - Gastroenterology
KW - Paediatric
KW - Ulcerative colitis
UR - http://www.scopus.com/inward/record.url?scp=85089569797&partnerID=8YFLogxK
U2 - 10.1007/s00431-020-03750-0
DO - 10.1007/s00431-020-03750-0
M3 - Article
C2 - 32813123
AN - SCOPUS:85089569797
SN - 0340-6199
VL - 179
SP - 1935
EP - 1944
JO - European Journal of Pediatrics
JF - European Journal of Pediatrics
IS - 12
ER -