Tildrakizumab Treatment Patterns in Adults With Moderate-to-Severe Plaque Psoriasis: A Retrospective Analysis From the Canadian Patient Support Program.

IF 3.5 3区 医学 Q1 DERMATOLOGY
Dermatology and Therapy Pub Date : 2025-08-01 Epub Date: 2025-05-29 DOI:10.1007/s13555-025-01434-x
Vimal H Prajapati, Nicole Bellefontaine, Devi Gopalan, Rommel Mangaser, Pak Chan, Maxwell B Sauder
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引用次数: 0

Abstract

Introduction: Tildrakizumab is an anti-interleukin-23 p19 monoclonal antibody approved in several countries to treat adult patients with moderate-to-severe plaque psoriasis who are candidates for phototherapy or systemic therapy. Limited data are available on tildrakizumab treatment patterns in clinical practice. The Canadian tildrakizumab patient support program (PSP), which provides personalized reimbursement, financial aid, and injection training support for disease management, was used in this study to evaluate real-world persistence and adherence to tildrakizumab.

Methods: This retrospective, observational study used data collected in the Canadian tildrakizumab PSP database between August 4, 2021, and August 1, 2023. Adult (≥18 years) patients with moderate-to-severe plaque psoriasis who enrolled in the PSP and received ≥6 months of treatment with tildrakizumab before August 1, 2023, were included. Data up to Week 52 following treatment initiation were analyzed. Persistence was defined as the number of days until treatment discontinuation. Adherence was measured as the proportion of days covered (PDC) from treatment initiation to treatment discontinuation or study cutoff, with PDC ≥80% indicating high adherence.

Results: The study included 813 patients with a mean ± standard deviation (SD) age of 49.6 ± 15.9 years; 55.0% (447/813) were male, and 92.7% (754/813) were biologic-naïve when initiating tildrakizumab. Patients received tildrakizumab treatment for a mean ± SD of 329.6 ± 55.0 days. After 1 year, 88.0% of patients were persistent on treatment. Adherence was also high, with mean ± SD PDC being 97.5% ± 8.9% and 93.5% of patients having PDC ≥80%. Eighty-five patients discontinued treatment, primarily because of switching to other therapies. Common adverse outcomes included treatment misuse (18.9%), disease flare (8.2%), and treatment discontinuation (7.4%).

Conclusion: Persistence and adherence to tildrakizumab were high through 52 weeks of treatment among patients with moderate-to-severe plaque psoriasis enrolled in the Canadian PSP.

Tildrakizumab治疗成人中至重度斑块性银屑病的模式:来自加拿大患者支持计划的回顾性分析
Tildrakizumab是一种抗白细胞介素- 23p19单克隆抗体,已在多个国家批准用于治疗中度至重度斑块性银屑病的成人患者,这些患者是光疗或全身治疗的候选人。在临床实践中,关于tildrakizumab治疗模式的数据有限。加拿大tildrakizumab患者支持项目(PSP)为疾病管理提供个性化报销、经济援助和注射培训支持,该项目在本研究中用于评估tildrakizumab在现实世界中的持久性和依从性。方法:这项回顾性观察性研究使用了2021年8月4日至2023年8月1日期间在加拿大tildrakizumab PSP数据库中收集的数据。纳入了在2023年8月1日前接受了≥6个月tildrakizumab治疗的成人(≥18岁)中度至重度斑块性银屑病患者。分析治疗开始后第52周的数据。持续时间定义为直到停止治疗的天数。依从性以从治疗开始到治疗停止或研究结束的覆盖天数(PDC)的比例来衡量,PDC≥80%表示高依从性。结果:纳入813例患者,平均±标准差(SD)年龄49.6±15.9岁;55.0%(447/813)为男性,92.7%(754/813)在开始使用tildrakizumab时为biologic-naïve。患者接受tildrakizumab治疗的平均±SD为329.6±55.0天。1年后,88.0%的患者坚持治疗。依从性也很高,平均±SD PDC为97.5%±8.9%,93.5%的患者PDC≥80%。85名患者停止治疗,主要是因为改用其他疗法。常见的不良结局包括治疗不当(18.9%)、疾病爆发(8.2%)和停止治疗(7.4%)。结论:在加拿大PSP研究中,接受52周治疗的中重度斑块型银屑病患者中,tildrakizumab的持久性和依从性很高。
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来源期刊
Dermatology and Therapy
Dermatology and Therapy Medicine-Dermatology
CiteScore
6.00
自引率
8.80%
发文量
187
审稿时长
6 weeks
期刊介绍: Dermatology and Therapy is an international, open access, peer-reviewed, rapid publication journal (peer review in 2 weeks, published 3–4 weeks from acceptance). The journal is dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of dermatological therapies. Studies relating to diagnosis, pharmacoeconomics, public health and epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to all clinical aspects of dermatology, such as skin pharmacology; skin development and aging; prevention, diagnosis, and management of skin disorders and melanomas; research into dermal structures and pathology; and all areas of aesthetic dermatology, including skin maintenance, dermatological surgery, and lasers. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports/case series, trial protocols, and short communications. Dermatology and 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 quality research, which may be considered of insufficient interest by other journals. The journal appeals to a global audience and receives submissions from all over the world.
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