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生物疗法在实现炎症性肠病治疗目标方面的有效性;来自中东地区的真实世界数据(ENROLL研究)。

Effectiveness of biologic therapies in achieving treatment targets in inflammatory bowel disease; real-world data from the Middle East (ENROLL study).

作者信息

Shehab Mohammad, Alfadhli Ahmad, Abdullah Israa, Alostad Wrood, Marei Alaa, Alrashed Fatema

机构信息

Department of Internal Medicine, Mubarak Al-Kabeer University Hospital, As Sālimīyah, Kuwait.

Department of Translational Research, Dasman Institute, Kuwait City, Kuwait.

出版信息

Front Pharmacol. 2024 Oct 16;15:1388043. doi: 10.3389/fphar.2024.1388043. eCollection 2024.

Abstract

BACKGROUND

Real-world data assessing the effectiveness of biologics in patients with inflammatory bowel disease (IBD) in the Middle East are not well-established. In our study, we evaluated the effectiveness of biologic therapies in achieving clinical and endoscopic outcomes in biologic-naïve patients with IBD.

DESIGN

A retrospective chart review was conducted at two tertiary care gastroenterology centers using electronic medical records of patients with moderate-to-severe IBD. The study period was from October 2017 to October 2023. Patients who were on infliximab, adalimumab, ustekinumab, or vedolizumab for 12 months were included in the analysis. The primary outcomes were the percentage of IBD-related hospitalizations or surgeries, achieving steroid-free remission, and endoscopic remission.

RESULTS

A total of 422 patients were included in the study, of whom 264 (62.5%) patients had Crohn's disease (CD) and 158 (39%) had ulcerative colitis (UC). In patients with CD, endoscopic remission was attained in 51 (52%) of the patients on adalimumab, 38 (53%) of the patients on infliximab, 34 (56%) of the patients on ustekinumab, and 16 (51%) of the patients on vedolizumab. In patients with UC, endoscopic remission was attained in 40 (56%) of the patients on infliximab, 26 (61%) of the patients on adalimumab, 8 (55%) of the patients on ustekinumab, and 11 (53%) of the patients on vedolizumab.

CONCLUSION

adalimumab, infliximab, ustekinumab, and vedolizumab were all effective in achieving clinical and endoscopic clinical outcomes in IBD in both UC and CD. The findings of this study suggest that the efficacy of biologics in a Middle Eastern population is similar to that in a Western population.

摘要

背景

评估生物制剂对中东地区炎症性肠病(IBD)患者有效性的真实世界数据尚不充分。在我们的研究中,我们评估了生物制剂疗法在初治IBD患者中实现临床和内镜结果的有效性。

设计

在两家三级医疗胃肠病中心进行了一项回顾性病历审查,使用中重度IBD患者的电子病历。研究期间为2017年10月至2023年10月。接受英夫利昔单抗、阿达木单抗、乌司奴单抗或维多珠单抗治疗12个月的患者纳入分析。主要结局是IBD相关住院或手术的百分比、实现无类固醇缓解和内镜缓解。

结果

共有422例患者纳入研究,其中264例(62.5%)为克罗恩病(CD)患者,158例(39%)为溃疡性结肠炎(UC)患者。在CD患者中,接受阿达木单抗治疗的患者中有51例(52%)实现内镜缓解,接受英夫利昔单抗治疗的患者中有38例(53%),接受乌司奴单抗治疗的患者中有34例(56%),接受维多珠单抗治疗的患者中有16例(51%)。在UC患者中,接受英夫利昔单抗治疗的患者中有40例(56%)实现内镜缓解,接受阿达木单抗治疗的患者中有26例(61%),接受乌司奴单抗治疗的患者中有8例(55%),接受维多珠单抗治疗的患者中有11例(53%)。

结论

阿达木单抗、英夫利昔单抗、乌司奴单抗和维多珠单抗在UC和CD的IBD患者中实现临床和内镜临床结果方面均有效。本研究结果表明,生物制剂在中东人群中的疗效与西方人群相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d39c/11521928/2254d83f3cd2/fphar-15-1388043-g001.jpg

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