Post-induction infliximab trough levels and disease activity in the clinical evolution of pediatric ulcerative colitis.
Adolescent
Child
Colectomy
/ statistics & numerical data
Colitis, Ulcerative
/ blood
Disease Progression
Dose-Response Relationship, Drug
Gastrointestinal Agents
/ administration & dosage
Humans
Infliximab
/ administration & dosage
Infusions, Intravenous
Maintenance Chemotherapy
/ methods
Retrospective Studies
Severity of Illness Index
Treatment Outcome
Young Adult
Infliximab
pediatrics
therapeutic drug monitoring
trough levels
ulcerative colitis
Journal
United European gastroenterology journal
ISSN: 2050-6414
Titre abrégé: United European Gastroenterol J
Pays: England
ID NLM: 101606807
Informations de publication
Date de publication:
05 2020
05 2020
Historique:
pubmed:
28
3
2020
medline:
29
6
2021
entrez:
28
3
2020
Statut:
ppublish
Résumé
Recent adult evidence suggests that infliximab (IFX) trough levels (TL) in patients with severe ulcerative colitis (UC) may be decreased. The aims of our study were to compare post-induction IFX TL of children with severe versus moderate UC and to evaluate short- and long-term outcomes. In this single-center retrospective study, children with a diagnosis of UC starting IFX with a Pediatric Ulcerative Colitis Activity Index (PUCAI) ≥35 and with available post-induction TL were recruited. UC characteristics, IFX dosage and interval, primary non-response, IFX failure, and surgery after 24 months were collected. Post induction TL, anti-IFX antibodies, and laboratory evaluations at the time of starting IFX were also acquired. A total of 90 children were enrolled, of whom 39 (43.3%) were classified as severe UC and 51 (56.6%) as moderate UC. Median post-induction IFX TL were lower in severe UC versus moderate group (5.5 vs 10.3; Children starting IFX with severe UC showed lower post-induction TL and poor disease outcomes. Achieving adequate TL was associated with better efficacy outcomes.
Sections du résumé
BACKGROUND AND AIMS
Recent adult evidence suggests that infliximab (IFX) trough levels (TL) in patients with severe ulcerative colitis (UC) may be decreased. The aims of our study were to compare post-induction IFX TL of children with severe versus moderate UC and to evaluate short- and long-term outcomes.
METHODS
In this single-center retrospective study, children with a diagnosis of UC starting IFX with a Pediatric Ulcerative Colitis Activity Index (PUCAI) ≥35 and with available post-induction TL were recruited. UC characteristics, IFX dosage and interval, primary non-response, IFX failure, and surgery after 24 months were collected. Post induction TL, anti-IFX antibodies, and laboratory evaluations at the time of starting IFX were also acquired.
RESULTS
A total of 90 children were enrolled, of whom 39 (43.3%) were classified as severe UC and 51 (56.6%) as moderate UC. Median post-induction IFX TL were lower in severe UC versus moderate group (5.5 vs 10.3;
CONCLUSIONS
Children starting IFX with severe UC showed lower post-induction TL and poor disease outcomes. Achieving adequate TL was associated with better efficacy outcomes.
Identifiants
pubmed: 32213038
doi: 10.1177/2050640620912877
pmc: PMC7226697
doi:
Substances chimiques
Gastrointestinal Agents
0
Infliximab
B72HH48FLU
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
425-435Références
Gastroenterology. 2008 Oct;135(4):1114-22
pubmed: 18725221
J Clin Gastroenterol. 2016 Oct;50(9):733-41
pubmed: 26535480
Gastroenterology. 2009 Oct;137(4):1250-60; quiz 1520
pubmed: 19596014
Clin Gastroenterol Hepatol. 2016 Apr;14(4):543-9
pubmed: 26681486
Inflamm Bowel Dis. 2015 Jan;21(1):182-97
pubmed: 25222660
Clin Gastroenterol Hepatol. 2015 Feb;13(2):336-8
pubmed: 25285408
J Crohns Colitis. 2018 Nov 15;12(11):1316-1325
pubmed: 30239644
J Pediatr Gastroenterol Nutr. 2014 Jun;58(6):795-806
pubmed: 24231644
Gastroenterology. 2007 Aug;133(2):423-32
pubmed: 17681163
Gastroenterology. 2010 Jun;138(7):2282-91
pubmed: 20193683
Inflamm Bowel Dis. 2019 Jun 18;25(7):1169-1186
pubmed: 30605549
Aliment Pharmacol Ther. 2013 Aug;38(3):294-302
pubmed: 23786158
Clin Gastroenterol Hepatol. 2007 Jan;5(1):103-10
pubmed: 17142106
J Crohns Colitis. 2019 Dec 10;13(12):1518-1526
pubmed: 31120524
Gastroenterology. 2017 Sep;153(3):835-857.e6
pubmed: 28774547
Aliment Pharmacol Ther. 2017 Mar;45(5):617-630
pubmed: 28074618
J Pediatr Gastroenterol Nutr. 2018 Aug;67(2):292-310
pubmed: 30044358
Gastroenterology. 2019 Oct;157(4):985-996.e2
pubmed: 31194979
Lancet. 2012 Dec 1;380(9857):1909-15
pubmed: 23063316
Inflamm Bowel Dis. 2011 Jun;17(6):1314-21
pubmed: 21560194
Gut. 2008 Mar;57(3):331-8
pubmed: 17981888
Am J Gastroenterol. 2009 Aug;104(8):2080-8
pubmed: 19436273
J Pediatr Gastroenterol Nutr. 2019 Jun;68(6):847-853
pubmed: 30633108
AAPS J. 2017 Jan;19(1):161-171
pubmed: 27600137
Inflamm Bowel Dis. 2016 Oct;22(10):2410-7
pubmed: 27537053
Clin Gastroenterol Hepatol. 2019 Feb;17(3):502-509.e1
pubmed: 29944926
Aliment Pharmacol Ther. 2016 Jun;43(12):1293-9
pubmed: 27091119
N Engl J Med. 2005 Dec 8;353(23):2462-76
pubmed: 16339095
Gut. 2018 Feb;67(2):237-243
pubmed: 28053054
Inflamm Bowel Dis. 2013 Feb;19(2):370-7
pubmed: 22570259
Gut. 2016 Feb;65(2):249-55
pubmed: 25670812
J Pediatr Gastroenterol Nutr. 2018 Oct;67(4):507-512
pubmed: 29901557
J Crohns Colitis. 2016 May;10(5):619-25
pubmed: 26763722
Dig Liver Dis. 2015 Jun;47(6):455-9
pubmed: 25733340
Gastroenterology. 2015 Aug;149(2):350-5.e2
pubmed: 25917786