Yiu Tsz Hong, Ko Yanna, Pudipeddi Aviv, Natale Patrizia, Leong Rupert W
Faculty of Medicine and Health, School of Public Health, The University of Sydney, Sydney, New South Wales, Australia
Western Sydney University, Campbelltown and Camden Hospitals, Sydney, Canterbury Hospital.
BMJ Open. 2023 Oct 3;13(10):e073071. doi: 10.1136/bmjopen-2023-073071.
Biological therapy is a cornerstone of managing moderate-to-severe inflammatory bowel disease (IBD), ulcerative colitis (UC) and Crohn's disease (CD). New biologics have been evolving over the past 20 years and selection of an agent remains challenging.Drug persistence measures the duration of time from initiation to discontinuation of a therapy, which can be a surrogate marker of drug tolerance and efficacy.
The study aimed to compare drug persistence of new generation biologics for the treatment of UC and CD (vedolizumab, ustekinumab, certolizumab, tofacitinib, natalizumab and golimumab) with conventional anti-tumor necroisis factor alphas (anti-TNF alphas) (adalimumab and infliximab) in adult patients with IBD. Results of the study may provide guidance on the preferred first and subsequent lines of biological treatments in patients with IBD.
Search via electronic databases including EMBASE, MEDLINE, PubMed and clinical trial databases will be conducted on 10 March 2023 with eligible studies included from inception of 2017 to 2023. The primary outcomes are 1-year persistence of individual biologics with comparison of new biologics versus conventional anti-TNF alphas. A meta-analysis will be conducted using Review Manager V.5 and outcome will be presented as relative risk. Heterogeneity will be assessed with forest plot, χ and I, followed with sensitivity analysis and subgroup analysis. Finally, the Grading of Recommendations Assessment, Development and Evaluation system will be used to assess the quality of evidence.
Ethical approval is not required as no private information of participants will be used. Results of the present study will be disseminated in a peer-reviewed journal or conference presentation.
CRD42023392236.
生物疗法是治疗中重度炎症性肠病(IBD)、溃疡性结肠炎(UC)和克罗恩病(CD)的基石。在过去20年中,新型生物制剂不断发展,选择一种药物仍然具有挑战性。药物持久性衡量从开始治疗到停止治疗的时间长度,它可以作为药物耐受性和疗效的替代指标。
本研究旨在比较新一代用于治疗UC和CD的生物制剂(维多珠单抗、乌司奴单抗、赛妥珠单抗、托法替布、那他珠单抗和戈利木单抗)与传统抗肿瘤坏死因子α(抗TNFα)制剂(阿达木单抗和英夫利昔单抗)在成年IBD患者中的药物持久性。该研究结果可能为IBD患者首选的一线及后续生物治疗方案提供指导。
将于2023年3月10日通过电子数据库进行检索,包括EMBASE、MEDLINE、PubMed和临床试验数据库,纳入自2017年开始至2023年的符合条件的研究。主要结局是各生物制剂的1年持久性,并比较新型生物制剂与传统抗TNFα制剂。将使用Review Manager V.5进行荟萃分析,结果将以相对风险表示。将通过森林图、χ²和I²评估异质性,随后进行敏感性分析和亚组分析。最后,将使用推荐分级评估、制定和评价系统来评估证据质量。
由于不会使用参与者个人信息,因此无需伦理批准。本研究结果将在同行评审期刊或会议报告中发表。
PROSPERO注册号:CRD42023392236。