Temporal Trends in the Use of Biological Agents in Patients with Inflammatory Bowel Disease: Real-World Data from a Tertiary Inflammatory Bowel Disease Greek Center During a 5-Year Period.

IF 2.9 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Journal of Clinical Medicine Pub Date : 2025-02-18 DOI:10.3390/jcm14041357
Panagiotis Markopoulos, Aikaterini Gaki, Georgios Kokkotis, Konstantina Chalakatevaki, Nikolaos Kioulos, Vasso Kitsou, Constantinos Tsitsigiannis, Michael Gizis, Paraskevi Prapa, Stamatina-Lydia Chatzinikolaou, Efrosini Laoudi, Ioannis Koutsounas, Giorgos Bamias
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Abstract

Background/Objectives: Therapeutic management of inflammatory bowel diseases (IBD) is rapidly evolving in the era of novel biological therapies. However, real-world data relating to the usage trends and treatment persistence remain inconsistent. This study aimed to investigate trends in biological use, dose intensification, and treatment persistence in IBD patients, who received treatment in a large tertiary center in Greece. Methods: Patients with IBD who underwent at least one biological treatment between 2018 and 2022 were included in this retrospective study. Data on patients' demographics, type of disease, use of biologicals, dose intensification, and treatment persistence were analyzed for time trends. Results: Data from 409 patients with IBD (mean age 39 (range 17-87), female 51%, 56.9% CD, mean duration of disease: 9.3 years) were included in the study. The number of patients on biologics was raised from 133 in 2018 to 368 in 2022 (a 28.1% yearly increase), while the percentage of patients who were treated with anti-TNF biosimilars increased to >60% of the total anti-TNF population in 2022. We observed a gradual increase in non-anti-TNF therapies in bio-naïve patients, in particular vedolizumab (46% of all biologicals in UC; 16% in CD) and ustekinumab (16.3% of all biologicals in UC, 31% in CD). The 3-year persistence rate of IFX was 64% in CD and 56% in UC, whereas it was 61% for ADA in CD. Dose intensification of anti-TNF was efficient in >50% of CD patients and >30% of UC patients; however, the majority of patients who required dose escalation within the first year eventually became unresponsive. The 3-year persistence of vedolizumab as a first-line treatment was 82% for CD and 69% for UC, respectively. The 3-year persistence of ustekinumab as first-line treatment for CD was 65%. No significant differences regarding the efficacy of anti-TNF, ustekinumab, or vedolizumab were detected when they were used as first-line treatments for Crohn's disease; similarly, no significant differences were detected between infliximab and vedolizumab as first-line treatments for UC. Conclusions: There was a gradual increase in the use of biologicals, including biosimilars, between the years 2018-2022, reflecting adherence to current guidance with adoption of an early escalation strategy. Newer, post-anti-TNF biologics such as vedolizumab and ustekinumab have been rapidly incorporated into therapeutic approaches for both CD and UC.

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炎症性肠病患者使用生物制剂的时间趋势:来自希腊三级炎症性肠病中心5年期间的真实世界数据
背景/目的:在新型生物疗法时代,炎症性肠病(IBD)的治疗管理正在迅速发展。然而,有关使用趋势和治疗持续性的真实数据仍然不一致。本研究旨在调查在希腊一家大型三级医疗中心接受治疗的IBD患者的生物使用、剂量强化和治疗持续性的趋势。方法:回顾性研究纳入2018年至2022年间至少接受过一次生物治疗的IBD患者。对患者的人口统计学、疾病类型、生物制剂的使用、剂量强化和治疗持续性等数据进行了时间趋势分析。结果:409例IBD患者(平均年龄39岁(17-87岁),女性占51%,CD占56.9%,平均病程9.3年)的数据被纳入研究。接受生物制剂治疗的患者数量从2018年的133人增加到2022年的368人(年增长率为28.1%),而接受抗tnf生物类似药治疗的患者比例在2022年增加到抗tnf总人群的60%。我们观察到bio-naïve患者的非抗tnf治疗逐渐增加,特别是vedolizumab(占UC所有生物制剂的46%;ustekinumab(占UC所有生物制剂的16.3%,占CD的31%)。IFX在CD中的3年持续率为64%,UC中的为56%,而ADA在CD中的3年持续率为61%。抗tnf剂量强化对50%的CD患者和30%的UC患者有效;然而,大多数需要在第一年内增加剂量的患者最终变得无反应。vedolizumab作为一线治疗的3年持续性分别为CD的82%和UC的69%。ustekinumab作为CD一线治疗的3年持续性为65%。抗肿瘤坏死因子、ustekinumab或vedolizumab作为克罗恩病的一线治疗时,其疗效未发现显著差异;同样,英夫利昔单抗和维多单抗作为UC的一线治疗也没有显著差异。结论:在2018-2022年期间,包括生物仿制药在内的生物制剂的使用逐渐增加,这反映了采用早期升级策略对现行指南的遵守。较新的抗肿瘤坏死因子后生物制剂,如vedolizumab和ustekinumab,已迅速纳入CD和UC的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Medicine
Journal of Clinical Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
5.70
自引率
7.70%
发文量
6468
审稿时长
16.32 days
期刊介绍: Journal of Clinical Medicine (ISSN 2077-0383), is an international scientific open access journal, providing a platform for advances in health care/clinical practices, the study of direct observation of patients and general medical research. This multi-disciplinary journal is aimed at a wide audience of medical researchers and healthcare professionals. Unique features of this journal: manuscripts regarding original research and ideas will be particularly welcomed.JCM also accepts reviews, communications, and short notes. There is no limit to publication length: our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible.
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