Switch from biosimilar infliximab CT-P13 to biosimilar infliximab SB-2 in the long-term maintenance therapy in IBD patients – prospective observational study

Q4 Medicine
Milan Lukáš, Veronika Hrubá, Jindra Reissigová, K. Černá, N. Machková, D. Ďuricová, M. Kolář, Lea Čermáková
{"title":"Switch from biosimilar infliximab CT-P13 to biosimilar infliximab SB-2 in the long-term maintenance therapy in IBD patients – prospective observational study","authors":"Milan Lukáš, Veronika Hrubá, Jindra Reissigová, K. Černá, N. Machková, D. Ďuricová, M. Kolář, Lea Čermáková","doi":"10.48095/ccgh2023336","DOIUrl":null,"url":null,"abstract":"Introduction: Therapeutical switch from originator to biosimilar infliximab has been proved as effective and safety procedure. We have a few information about non-medical swich from one biosimilar to the another biosimilar infiximab. Aim: This is a prospective observational study from one tercial IBD center, performed in 2021 and 2022 which was focused on efficacy and safety after switch from infliximab CT-P13 to infliximab SB-2 in patients with IBD. Methods: The cohort group comprised with 287 patients with IBD who have been consecutively treated with infliximab CT-P13 and they were switched to infliximab SB-2. All the re cruited patients were in clinical and biological sustained remission at mean for 6 months before the switch. Results: We proved that persistence on infliximab SB-2 therapy after the switch was 86.4% of treated patients, no significant changes in clinical inflammatory activities and biological parameters have been detected after the switch. The therapy termination due to side effects or loss of response in 39 patients (13.9%) has been detected due to lost of clinical response, side effects or lost of follow-up. No higher immunogenicity after the switch was found. Conclusion: Non-medical switch from one biosimilar infliximab (CT-P13) to another one (SB-2) was not associated with higher risks of disease destabilisation or immunogenicity. Keywords inflammatory bowel disease, biosimilar infliximab CT-P13, biosimilar infliximab SB-2, therapeutical switch","PeriodicalId":38577,"journal":{"name":"Gastroenterologie a Hepatologie","volume":"16 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gastroenterologie a Hepatologie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.48095/ccgh2023336","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Therapeutical switch from originator to biosimilar infliximab has been proved as effective and safety procedure. We have a few information about non-medical swich from one biosimilar to the another biosimilar infiximab. Aim: This is a prospective observational study from one tercial IBD center, performed in 2021 and 2022 which was focused on efficacy and safety after switch from infliximab CT-P13 to infliximab SB-2 in patients with IBD. Methods: The cohort group comprised with 287 patients with IBD who have been consecutively treated with infliximab CT-P13 and they were switched to infliximab SB-2. All the re cruited patients were in clinical and biological sustained remission at mean for 6 months before the switch. Results: We proved that persistence on infliximab SB-2 therapy after the switch was 86.4% of treated patients, no significant changes in clinical inflammatory activities and biological parameters have been detected after the switch. The therapy termination due to side effects or loss of response in 39 patients (13.9%) has been detected due to lost of clinical response, side effects or lost of follow-up. No higher immunogenicity after the switch was found. Conclusion: Non-medical switch from one biosimilar infliximab (CT-P13) to another one (SB-2) was not associated with higher risks of disease destabilisation or immunogenicity. Keywords inflammatory bowel disease, biosimilar infliximab CT-P13, biosimilar infliximab SB-2, therapeutical switch
从生物类似药英夫利昔单抗CT-P13到生物类似药英夫利昔单抗SB-2在IBD患者长期维持治疗中的转换——前瞻性观察研究
从原药到生物仿制药英夫利昔单抗的治疗转换已被证明是有效和安全的程序。我们有一些关于从一种生物仿制药到另一种生物仿制药的非医学转换的信息。目的:这是一项来自一家IBD中心的前瞻性观察性研究,于2021年和2022年进行,重点是IBD患者从英夫利昔单抗CT-P13切换到英夫利昔单抗SB-2后的疗效和安全性。方法:队列组由287例IBD患者组成,这些患者连续接受英夫利昔单抗CT-P13治疗,然后切换到英夫利昔单抗SB-2。所有重新招募的患者在转换前平均6个月处于临床和生物学持续缓解状态。结果:我们证明切换后坚持英夫利昔单抗SB-2治疗的患者占86.4%,切换后未检测到临床炎症活动和生物学参数的明显变化。39例(13.9%)患者因无临床反应、无副作用或无随访而终止治疗。转换后没有发现更高的免疫原性。结论:从一种英夫利昔单抗生物仿制药(CT-P13)到另一种生物仿制药(SB-2)的非医疗转换与疾病不稳定或免疫原性的高风险无关。炎症性肠病;英夫利昔单抗生物仿制药CT-P13;英夫利昔单抗生物仿制药SB-2
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Gastroenterologie a Hepatologie
Gastroenterologie a Hepatologie Medicine-Gastroenterology
CiteScore
0.40
自引率
0.00%
发文量
32
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信