Frontiers in Immunology (Feb 2024)

Comparison of endoscopic healing and durability between infliximab originator and CT-P13 in pediatric patients with inflammatory bowel disease

  • Eun Sil Kim,
  • Sujin Choi,
  • Sujin Choi,
  • Byung-Ho Choe,
  • Byung-Ho Choe,
  • Sowon Park,
  • Yeoun Joo Lee,
  • Sang Jun Sohn,
  • Soon Chul Kim,
  • Ki Soo Kang,
  • Kunsong Lee,
  • Jung Ok Shim,
  • Yu Bin Kim,
  • Suk Jin Hong,
  • Suk Jin Hong,
  • Yoo Min Lee,
  • Hyun Jin Kim,
  • So Yoon Choi,
  • Ju Young Kim,
  • Yoon Lee,
  • Ji-Sook Park,
  • Ji-Sook Park,
  • Jae Young Kim,
  • Dae Yong Yi,
  • Ji Hyuk Lee,
  • Kwang-Hae Choi,
  • Kwang-Hae Choi,
  • Hyo-Jeong Jang,
  • Hyo-Jeong Jang,
  • In Sook Jeong,
  • Ben Kang,
  • Ben Kang

DOI
https://doi.org/10.3389/fimmu.2024.1284181
Journal volume & issue
Vol. 15

Abstract

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Background and aimsFavourable clinical data were published on the efficacy of CT-P13, the first biosimilar of infliximab (IFX), in pediatric inflammatory bowel disease (IBD); however, few studies have compared the effect on endoscopic healing (EH) and drug retention rate between the IFX originator and CT-P13. Therefore, we aimed to compare EH and the drug retention rate between the IFX originator and CT-P13.MethodsChildren with Crohn’s disease (CD) and ulcerative colitis (UC)/IBD-unclassified (IBD-U) at 22 medical centers were enrolled, with a retrospective review conducted at 1-year and last follow-up. Clinical remission, EH and drug retention rate were evaluated.ResultsWe studied 416 pediatric patients with IBD: 77.4% had CD and 22.6% had UC/IBD-U. Among them, 255 (61.3%) received the IFX originator and 161 (38.7%) received CT-P13. No statistically significant differences were found between the IFX originator and CT-P13 in terms of corticosteroid-free remission and adverse events. At 1-year follow-up, EH rates were comparable between them (CD: P=0.902, UC: P=0.860). The estimated cumulative cessation rates were not significantly different between the two groups. In patients with CD, the drug retention rates were 66.1% in the IFX originator and 71.6% in the CT-P13 group at the maximum follow-up period (P >0.05). In patients with UC, the drug retention rates were 49.8% in the IFX originator and 56.3% in the CT-P13 group at the maximum follow-up period (P >0.05).ConclusionsThe IFX originator and CT-P13 demonstrated comparable therapeutic response including EH, clinical remission, drug retention rate and safety in pediatric IBD.

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