• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

炎症性肠病靶向治疗的使用趋势:ENEIDA的TRENDY研究

Trends in Targeted Therapy Usage in Inflammatory Bowel Disease: TRENDY Study of ENEIDA.

作者信息

Gómez-Labrador Celia, Ricart Elena, Iborra Marisa, Iglesias Eva, Martín-Arranz María Dolores, de Castro Luisa, De Francisco Ruth, García-Alonso Francisco Javier, Sanahuja Ana, Gargallo-Puyuelo Carla J, Mesonero Francisco, Casanova María José, Mañosa Míriam, Rivero Montserrat, Calvo Marta, Sierra-Ausin Mónica, González-Muñoza Carlos, Calvet Xavier, García-López Santiago, Guardiola Jordi, Arias García Lara, Márquez-Mosquera Lucía, Gutiérrez Ana, Zabana Yamile, Navarro-Llavat Mercè, Lorente Poyatos Rufo, Piqueras Marta, Torrealba Leyanira, Bermejo Fernando, Ponferrada-Díaz Ángel, Pérez-Calle José L, Barreiro-de Acosta Manuel, Tejido Coral, Cabriada José Luis, Marín-Jiménez Ignacio, Roncero Óscar, Ber Yolanda, Fernández-Salazar Luis, Camps Aler Blau, Lucendo Alfredo J, Llaó Jordina, Bujanda Luis, Muñoz Villafranca Carmen, Domènech Eugeni, Chaparro María, Gisbert Javier P

机构信息

Gastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid and Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), 28006 Madrid, Spain.

Gastroenterology Unit, Hospital Clinic of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) and CIBEREHD, 08036 Barcelona, Spain.

出版信息

Pharmaceutics. 2024 May 8;16(5):629. doi: 10.3390/pharmaceutics16050629.

DOI:10.3390/pharmaceutics16050629
PMID:38794292
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11124941/
Abstract

Markers that allow for the selection of tailored treatments for individual patients with inflammatory bowel diseases (IBD) are yet to be identified. Our aim was to describe trends in real-life treatment usage. For this purpose, patients from the ENEIDA registry who received their first targeted IBD treatment (biologics or tofacitinib) between 2015 and 2021 were included. A subsequent analysis with Machine Learning models was performed. The study included 10,009 patients [71% with Crohn's disease (CD) and 29% with ulcerative colitis (UC)]. In CD, anti-TNF (predominantly adalimumab) were the main agents in the 1st line of treatment (LoT), although their use declined over time. In UC, anti-TNF (mainly infliximab) use was predominant in 1st LoT, remaining stable over time. Ustekinumab and vedolizumab were the most prescribed drugs in 2nd and 3rd LoT in CD and UC, respectively. Overall, the use of biosimilars increased over time. Machine Learning failed to identify a model capable of predicting treatment patterns. In conclusion, drug positioning is different in CD and UC. Anti-TNF were the most used drugs in IBD 1st LoT, being adalimumab predominant in CD and infliximab in UC. Ustekinumab and vedolizumab have gained importance in CD and UC, respectively. The approval of biosimilars had a significant impact on treatment.

摘要

能够为炎症性肠病(IBD)个体患者选择量身定制治疗方案的标志物尚未确定。我们的目的是描述实际治疗使用情况的趋势。为此,纳入了ENEIDA注册中心在2015年至2021年间接受首次靶向IBD治疗(生物制剂或托法替布)的患者。随后进行了机器学习模型分析。该研究纳入了10009名患者[71%为克罗恩病(CD),29%为溃疡性结肠炎(UC)]。在CD中,抗TNF(主要是阿达木单抗)是一线治疗(LoT)的主要药物,不过其使用随时间有所下降。在UC中,抗TNF(主要是英夫利昔单抗)在一线治疗中占主导地位,且随时间保持稳定。乌司奴单抗和维多珠单抗分别是CD和UC二线及三线治疗中处方最多的药物。总体而言,生物类似药的使用随时间增加。机器学习未能识别出能够预测治疗模式的模型。总之,CD和UC中的药物定位有所不同。抗TNF是IBD一线治疗中使用最多的药物,在CD中以阿达木单抗为主,在UC中以英夫利昔单抗为主。乌司奴单抗和维多珠单抗分别在CD和UC中变得越来越重要。生物类似药的获批对治疗产生了重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/d12f8a06fae0/pharmaceutics-16-00629-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/e7822611df62/pharmaceutics-16-00629-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/4b17c5706c95/pharmaceutics-16-00629-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/6584259bb294/pharmaceutics-16-00629-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/d12f8a06fae0/pharmaceutics-16-00629-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/e7822611df62/pharmaceutics-16-00629-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/4b17c5706c95/pharmaceutics-16-00629-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/6584259bb294/pharmaceutics-16-00629-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e27/11124941/d12f8a06fae0/pharmaceutics-16-00629-g004.jpg

相似文献

1
Trends in Targeted Therapy Usage in Inflammatory Bowel Disease: TRENDY Study of ENEIDA.炎症性肠病靶向治疗的使用趋势:ENEIDA的TRENDY研究
Pharmaceutics. 2024 May 8;16(5):629. doi: 10.3390/pharmaceutics16050629.
2
Superior treatment persistence with ustekinumab in Crohn's disease and vedolizumab in ulcerative colitis compared with anti-TNF biological agents: real-world registry data from the Persistence Australian National IBD Cohort (PANIC) study.与抗 TNF 生物制剂相比,乌司奴单抗治疗克罗恩病和维得利珠单抗治疗溃疡性结肠炎的持续治疗效果更好:来自真实世界的澳大利亚国家 IBD 队列(PANIC)研究的持久性注册数据。
Aliment Pharmacol Ther. 2021 Aug;54(3):292-301. doi: 10.1111/apt.16436. Epub 2021 Jun 20.
3
Drug utilization of biologic therapy in Crohn's disease and ulcerative colitis: a population-based Danish cohort study 2015-2020.2015-2020 年丹麦基于人群的队列研究:生物治疗在克罗恩病和溃疡性结肠炎中的药物利用情况。
Scand J Gastroenterol. 2023 Jul;58(7):726-736. doi: 10.1080/00365521.2023.2173988. Epub 2023 Feb 21.
4
Comparative effectiveness of second-line biological therapies for ulcerative colitis and Crohn's disease in patients with prior failure of anti-tumour necrosis factor treatment.对比在抗肿瘤坏死因子治疗失败的患者中,二线生物治疗药物对于溃疡性结肠炎和克罗恩病的疗效。
BMC Gastroenterol. 2022 Mar 27;22(1):143. doi: 10.1186/s12876-022-02225-w.
5
10 years of biologic use patterns in patients with inflammatory bowel disease: treatment persistence, switching and dose intensification - a nationwide population-based study.炎症性肠病患者生物制剂使用模式的10年:治疗持续性、转换和剂量强化——一项基于全国人口的研究
Therap Adv Gastroenterol. 2023 Sep 29;16:17562848231201728. doi: 10.1177/17562848231201728. eCollection 2023.
6
Real-World Treatment Patterns and Physician Preferences for Biologics in Moderate-to-Severe Inflammatory Bowel Disease: Retrospective Chart Review in Europe.中重度炎症性肠病生物制剂的真实世界治疗模式及医生偏好:欧洲的回顾性病历审查
Crohns Colitis 360. 2022 Jan 27;4(1):otac001. doi: 10.1093/crocol/otac001. eCollection 2022 Jan.
7
8
Effectiveness of vedolizumab and ustekinumab as second biologic agent in achieving target outcomes in tumor necrosis factor antagonists experienced patients with inflammatory bowel disease (enroll-ex study).维多珠单抗和优特克单抗作为第二种生物制剂在肿瘤坏死因子拮抗剂治疗失败的炎症性肠病患者中实现目标结局的有效性(ENROLL-EX研究)
Front Pharmacol. 2023 Oct 9;14:1243080. doi: 10.3389/fphar.2023.1243080. eCollection 2023.
9
First-line biologic treatment of inflammatory bowel disease during the first 12 months after diagnosis from 2010 to 2016: a Norwegian nationwide registry study.2010 年至 2016 年诊断后 12 个月内炎症性肠病的一线生物治疗:一项挪威全国登记研究。
Scand J Gastroenterol. 2021 Oct;56(10):1163-1168. doi: 10.1080/00365521.2021.1955147. Epub 2021 Jul 28.
10
Budget Impact of Adding Vedolizumab to a Health Plan Formulary as Another First-Line Biologic Option for Ulcerative Colitis and Crohn's Disease.将维多珠单抗添加到健康计划处方中作为溃疡性结肠炎和克罗恩病的另一种一线生物制剂选择的预算影响
Am Health Drug Benefits. 2018 Jul;11(5):253-262.

本文引用的文献

1
Real-world outcomes of switching from adalimumab originator to adalimumab biosimilar in patients with inflammatory bowel disease: The ADA-SWITCH study.炎症性肠病患者从阿达木单抗原研药转换为阿达木单抗生物类似药的真实世界结局:ADA-SWITCH 研究。
Aliment Pharmacol Ther. 2023 Jul;58(1):60-70. doi: 10.1111/apt.17525. Epub 2023 Apr 23.
2
The cost of inflammatory bowel disease in high-income settings: a Lancet Gastroenterology & Hepatology Commission.高收入国家炎症性肠病的成本:柳叶刀胃肠病学与肝脏病学委员会报告
Lancet Gastroenterol Hepatol. 2023 May;8(5):458-492. doi: 10.1016/S2468-1253(23)00003-1. Epub 2023 Mar 2.
3
Drug utilization of biologic therapy in Crohn's disease and ulcerative colitis: a population-based Danish cohort study 2015-2020.
2015-2020 年丹麦基于人群的队列研究:生物治疗在克罗恩病和溃疡性结肠炎中的药物利用情况。
Scand J Gastroenterol. 2023 Jul;58(7):726-736. doi: 10.1080/00365521.2023.2173988. Epub 2023 Feb 21.
4
Ustekinumab versus adalimumab for induction and maintenance therapy in biologic-naive patients with moderately to severely active Crohn's disease: a multicentre, randomised, double-blind, parallel-group, phase 3b trial.乌司奴单抗与阿达木单抗用于生物初治中重度活动型克罗恩病患者诱导缓解和维持治疗的比较:一项多中心、随机、双盲、平行分组、3b 期临床试验。
Lancet. 2022 Jun 11;399(10342):2200-2211. doi: 10.1016/S0140-6736(22)00688-2.
5
Emerging role of biosimilars in the clinical care of inflammatory bowel disease patients.生物类似药在炎症性肠病患者临床治疗中的新作用。
World J Clin Cases. 2022 May 16;10(14):4327-4333. doi: 10.12998/wjcc.v10.i14.4327.
6
How to Choose the Biologic Therapy in a Bio-naïve Patient with Inflammatory Bowel Disease.如何为初治的炎症性肠病患者选择生物治疗方法。
J Clin Med. 2022 Feb 4;11(3):829. doi: 10.3390/jcm11030829.
7
The Future of Precision Medicine to Predict Outcomes and Control Tissue Remodeling in Inflammatory Bowel Disease.精准医学在预测炎症性肠病结局和控制组织重塑中的未来。
Gastroenterology. 2022 Apr;162(5):1525-1542. doi: 10.1053/j.gastro.2021.09.077. Epub 2022 Jan 4.
8
Trends in the use of biologicals and their treatment outcomes among patients with inflammatory bowel diseases - a Danish nationwide cohort study.炎症性肠病患者使用生物制剂及其治疗结果的趋势-一项丹麦全国队列研究。
Aliment Pharmacol Ther. 2022 Mar;55(5):541-557. doi: 10.1111/apt.16723. Epub 2021 Dec 8.
9
Primary Failure to an Anti-TNF Agent in Inflammatory Bowel Disease: Switch (to a Second Anti-TNF Agent) or Swap (for Another Mechanism of Action)?炎症性肠病中抗TNF药物的原发性失效:更换(为第二种抗TNF药物)还是替换(为另一种作用机制的药物)?
J Clin Med. 2021 Nov 15;10(22):5318. doi: 10.3390/jcm10225318.
10
AGA Technical Review on the Medical Management of Moderate to Severe Luminal and Perianal Fistulizing Crohn's Disease.AGA 技术评论:中重度肠腔和肛旁瘘管型克罗恩病的医学管理
Gastroenterology. 2021 Jun;160(7):2512-2556.e9. doi: 10.1053/j.gastro.2021.04.023.