TY - JOUR
T1 - Prognosis of pediatric ulcerative colitis after infliximab failure
T2 - A multicenter registry-based cohort study
AU - Nambu, Ryusuke
AU - Kudo, Takahiro
AU - Tachibana, Nao
AU - Shimizu, Hirotaka
AU - Mizuochi, Tatsuki
AU - Kato, Sawako
AU - Inoue, Mikihiro
AU - Kumagai, Hideki
AU - Ishige, Takashi
AU - Kunisaki, Reiko
AU - Noguchi, Atsuko
AU - Yodoshi, Toshifumi
AU - Hagiwara, Shin Ichiro
AU - Nishimata, Shigeo
AU - Kakuta, Fumihiko
AU - Saito, Takeshi
AU - Iwama, Itaru
AU - Hirano, Yuri
AU - Shimizu, Toshiaki
AU - Arai, Katsuhiro
AU - Hara, Tomoko
AU - Jimbo, Keisuke
AU - Takaki, Yugo
AU - Nakayama, Yoshiko
AU - Uchida, Keiichi
AU - Yokoyama, Koji
AU - Ogashiwa, Tsuyoshi
N1 - Publisher Copyright:
© 2023 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.
PY - 2024/2
Y1 - 2024/2
N2 - Background and Aim: Even with increasing numbers of biologic agents available for management of ulcerative colitis (UC), infliximab (IFX) retains an important place in treatment of pediatric patients with this disease. As few reports have addressed outcomes in pediatric UC patients who had to discontinue IFX, we examined clinical course and prognosis after IFX failure in pediatric UC. Methods: A prospective cohort study of pertinent cases enrolled in the Japanese Pediatric Inflammatory Bowel Disease Registry between 2012 and 2020 was conducted to determine outcomes for pediatric UC patients who received IFX but required its discontinuation during follow-up (IFX failure). Results: Of the 301 pediatric UC patients in the registry, 75 were treated with IFX; in 36 of these, IFX was discontinued during follow-up. Severity of UC at onset and absence of concomitant immunomodulator therapy were significant risk factors for IFX failure (P = 0.005 and P = 0.02, respectively). The cumulative colectomy rate after IFX failure was 41.3% at 1 year and 47.5% at 2 years. Colectomy was significantly more frequent when IFX was discontinued before June 1, 2018, than when IFX was discontinued later (P = 0.013). This difference likely involves availability of additional biologic agents for treatment of UC beginning in mid-2018 (P = 0.005). Conclusion: In pediatric UC patients, approximately 50% underwent colectomy during a 2-year interval following IFX failure. Prognosis after IFX failure appeared to improve with availability of new biologic agents and small-molecule drugs in mid-2018.
AB - Background and Aim: Even with increasing numbers of biologic agents available for management of ulcerative colitis (UC), infliximab (IFX) retains an important place in treatment of pediatric patients with this disease. As few reports have addressed outcomes in pediatric UC patients who had to discontinue IFX, we examined clinical course and prognosis after IFX failure in pediatric UC. Methods: A prospective cohort study of pertinent cases enrolled in the Japanese Pediatric Inflammatory Bowel Disease Registry between 2012 and 2020 was conducted to determine outcomes for pediatric UC patients who received IFX but required its discontinuation during follow-up (IFX failure). Results: Of the 301 pediatric UC patients in the registry, 75 were treated with IFX; in 36 of these, IFX was discontinued during follow-up. Severity of UC at onset and absence of concomitant immunomodulator therapy were significant risk factors for IFX failure (P = 0.005 and P = 0.02, respectively). The cumulative colectomy rate after IFX failure was 41.3% at 1 year and 47.5% at 2 years. Colectomy was significantly more frequent when IFX was discontinued before June 1, 2018, than when IFX was discontinued later (P = 0.013). This difference likely involves availability of additional biologic agents for treatment of UC beginning in mid-2018 (P = 0.005). Conclusion: In pediatric UC patients, approximately 50% underwent colectomy during a 2-year interval following IFX failure. Prognosis after IFX failure appeared to improve with availability of new biologic agents and small-molecule drugs in mid-2018.
UR - https://www.scopus.com/pages/publications/85178958428
UR - https://www.scopus.com/inward/citedby.url?scp=85178958428&partnerID=8YFLogxK
U2 - 10.1111/jgh.16431
DO - 10.1111/jgh.16431
M3 - Article
C2 - 38058020
AN - SCOPUS:85178958428
SN - 0815-9319
VL - 39
SP - 312
EP - 318
JO - Journal of Gastroenterology and Hepatology (Australia)
JF - Journal of Gastroenterology and Hepatology (Australia)
IS - 2
ER -