Real-World Long-Term Persistence and Surgical Procedure-Free Period Among Bio-naïve Patients with Crohn’s Disease and Fistula Initiated on Ustekinumab

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Advances in Therapy Pub Date : 2024-08-20 DOI:10.1007/s12325-024-02963-1
Maryia Zhdanava, Sumesh Kachroo, Porpong Boonmak, Sabree Burbage, Aditi Shah, Patrick Lefebvre, Caroline Kerner, Dominic Pilon
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Abstract

Introduction

Fistula is a common complication of Crohn’s disease (CD). Treatment with biologics has been associated with fistula healing. Long-term persistence is an important factor for a chronic inflammatory process such as fistula. This study described 24-month persistence and time-to-surgery endpoints among bio-naïve patients with CD and intestinal fistula who were initiated on ustekinumab.

Methods

Adults with CD and any enteric or perianal fistula initiated on ustekinumab (index date) between September 23, 2016, and March 2, 2022, were selected from the IQVIA PharMetrics® Plus database and followed up to 24 months. Persistence on ustekinumab (no gaps in days of supply of > 120 days) and composite endpoints of being persistent while on monotherapy and persistent while corticosteroid free were also assessed. The date of surgery was defined as the date of first claim for any CD-related surgeries. Persistence and time-to-surgery endpoints were assessed from the index date until the earliest of discontinuation (event), immunomodulator or other biologic use (event), corticosteroid use (event), date of surgery (event), 24-month follow-up or data end (censoring) using Kaplan-Meier analyses.

Results

The sample included 445 patients (mean age: 42.8 years; 56.6% female). The most common type of fistula was anal fistula (36.0%). At 24 months after ustekinumab initiation, 64.2% of patients remained persistent (95% confidence interval [CI] 55.8–71.4). Furthermore, 53.3% of patients were persistent while on monotherapy (95% CI 45.1–60.7), and 45.6% of patients were persistent while being corticosteroid free (95% CI 36.9–53.8). At 24 months, 22.8% (95% CI 17.0–30.3) of patients underwent any CD-related surgery.

Conclusion

This study quantified long-term persistence on ustekinumab among bio-naïve patients with CD and fistula. Over half of patients initiated on ustekinumab were persistent and persistent while on monotherapy 24 months after initiation. Time-to-surgery estimate was comparable to existing evidence. These findings support ustekinumab as a treatment option for long-term management of CD with fistula.

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克罗恩病和瘘管的生物无效患者开始使用乌司替库单抗后的长期疗效和无手术期的实际情况。
简介:瘘管是克罗恩病(CD)的常见并发症:瘘管是克罗恩病(CD)的常见并发症。使用生物制剂治疗与瘘管愈合有关。长期持续性是瘘管等慢性炎症过程的一个重要因素。本研究描述了开始使用乌司替尼的CD和肠瘘患者24个月的持续性和手术时间终点:从IQVIA PharMetrics® Plus数据库中选取2016年9月23日至2022年3月2日期间开始使用乌司替库单抗(指标日期)的CD合并任何肠瘘或肛周瘘的成人患者,随访24个月。此外,还评估了持续服用乌司替库单抗的情况(供应天数间隔未超过 120 天),以及持续服用单药和持续服用无皮质类固醇药物的复合终点。手术日期定义为首次申请 CD 相关手术的日期。采用卡普兰-梅耶尔分析法评估了从指数日期到停药(事件)、使用免疫调节剂或其他生物制剂(事件)、使用皮质类固醇(事件)、手术日期(事件)、24 个月随访或数据结束(剔除)最早日期的持续性和手术时间终点:样本包括 445 名患者(平均年龄:42.8 岁;56.6% 为女性)。最常见的瘘管类型是肛瘘(36.0%)。在开始使用乌司替库单抗 24 个月后,64.2% 的患者瘘管仍然存在(95% 置信区间 [CI] 55.8-71.4)。此外,53.3%的患者在接受单药治疗时病情仍在持续(95% 置信区间 [CI] 45.1-60.7),45.6%的患者在不使用皮质类固醇时病情仍在持续(95% 置信区间 [CI] 36.9-53.8)。24个月时,22.8%(95% CI 17.0-30.3)的患者接受了任何与CD相关的手术:这项研究对CD合并瘘管的生物无效患者长期服用乌司替尼的情况进行了量化。在开始使用乌司替库单抗的患者中,超过半数的患者在开始使用单药治疗 24 个月后仍在坚持使用乌司替库单抗。估计的手术时间与现有证据相当。这些研究结果支持将乌司替库单抗作为CD合并瘘管长期治疗的一种治疗选择。
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
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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