影响日本银屑病患者使用生物制剂坚持治疗的因素:利用保险理赔数据库进行的真实世界研究。

IF 3.5 3区 医学 Q1 DERMATOLOGY
Dermatology and Therapy Pub Date : 2024-11-01 Epub Date: 2024-10-15 DOI:10.1007/s13555-024-01274-1
Celine Miyazaki, Junya Masuda, Phiona I-Ching Tsai, Hidehisa Saeki
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引用次数: 0

摘要

导言:对于包括银屑病(PsO)在内的慢性疾病而言,生物制剂治疗的不良持续性可能导致不理想的健康结果和更大的经济负担。在日本,评估银屑病患者生物制剂治疗持续性因素的研究非常有限。我们在真实世界环境中评估了银屑病患者的生物制剂治疗持续率(中位治疗时间和总体治疗存活率)和相关因素:这项对日本医疗数据中心(JMDC)数据库中保险理赔记录的回顾性分析纳入了年龄≥18岁、接受过生物制剂治疗的PsO患者[国际疾病分类(ICD)代码:L40.x]。利用2016年至2020年的数据,按生物制剂类别和单个生物制剂(英夫利昔单抗、阿达木单抗、乌斯替库单抗、古谢库单抗、secukinumab、ixekizumab和brodalumab)分析了生物制剂无经验患者(在索引中启动首个生物制剂)和生物制剂有经验患者的治疗持续率。采用卡普兰-梅耶生存率(治疗持续率)和多变量考克斯比例危险回归(预测因素)分析:共纳入了 1528 名 PsO 患者(平均年龄 47.4 岁)。在接受评估的生物制剂中,英夫利西单抗的中位治疗时间最长(33.6个月),而布达鲁单抗的中位治疗时间最短(9.7个月)。在接受评估的生物制剂中,古舍库单抗的1年治疗存活率最高(83%),而布达鲁单抗最低(45%)。有生物治疗经验的患者的中位治疗时间略长于无生物治疗经验的患者(22.8 个月对 18.1 个月)。性别[男性;危险比(HR)0.84,p = 0.016]和特定的PsO诊断代码,如L40.0(寻常型PsO;HR 0.69;p = 0.006)、L40.1(全身脓疱型PsO;HR 0.75;p = 0.034)和L40.9(未指定的PsO;HR 0.72;p = 0.001),是预测治疗持续性的因素。同时,年龄和Charlson综合指数评分分别与阿达木单抗和英夫利西单抗的治疗持续性显著相关:结论:在接受评估的生物制剂中,英夫利西单抗的中位治疗时间最长,古谢库单抗的1年治疗存活率最高。性别和特定的 PsO 诊断代码会影响总体治疗持续时间。这些发现可为实际临床环境中的PsO长期治疗计划提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Affecting Treatment Persistence in Japanese Patients with Psoriasis Prescribed Biologics: A Real-World Study Using an Insurance Claim Database.

Introduction: Poor persistence to biologics can result in suboptimal health outcomes and increased economic burden for chronic conditions, including psoriasis (PsO). In Japan, studies evaluating factors responsible for biologic treatment persistence in patients with PsO are limited. We assessed biologic treatment persistence (median treatment duration and overall treatment survival) and associated factors in patients with PsO in a real-world setting.

Methods: This retrospective analysis of insurance claims records from the Japan Medical Data Center (JMDC) database included patients with PsO [International Classification of Diseases (ICD) code: L40.x] ≥ 18 years of age who had received biologic treatment. Treatment persistence was analyzed using data from 2016 to 2020 by biologic class and by individual biologics (infliximab, adalimumab, ustekinumab, guselkumab, secukinumab, ixekizumab, and brodalumab) in bio-naïve (who initiate first biologic at index) and bio-experienced patients. Kaplan-Meier survival (treatment persistence), and multivariate Cox proportional hazard regression (predictive factors) analyses were used.

Results: Overall, 1528 patients with PsO were included (mean age 47.4 years). Infliximab had the longest median treatment duration (33.6 months), while brodalumab had the shortest (9.7 months) among biologics evaluated. Of the biologics evaluated, 1-year treatment survival was highest with guselkumab (83%), and lowest with brodalumab (45%). Bio-experienced patients showed slightly longer median treatment duration than bio-naïve patients (22.8 versus 18.1 months). Factors predictive of treatment persistence were sex [male; hazard ratio (HR) 0.84, p = 0.016] and specific PsO diagnostic codes, such as L40.0 (PsO vulgaris; HR 0.69; p = 0.006), L40.1 (generalized pustular PsO; HR 0.75; p = 0.034), and L40.9 (PsO unspecified; HR 0.72; p = 0.001). Meanwhile, age and Charlson Comorbidity Index score were significantly associated with adalimumab and infliximab treatment persistence, respectively.

Conclusion: Among biologics evaluated, infliximab had the longest median treatment duration, and guselkumab had the highest 1-year treatment survival. Sex and specific PsO diagnostic codes influenced overall treatment persistence. These findings could inform long-term treatment plans for PsO in real-world clinical settings.

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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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