Retention rate of TNF inhibitors versus IL-17 inhibitors in ankylosing spondylitis patients with prior biologics experience.

IF 4.6 2区 医学 Q1 Medicine
Jiwon Yang, Bong-Woo Lee, Youngjae Park, Ji Hyeon Ju, Wan-Uk Kim, Sung-Hwan Park, Seung-Ki Kwok, Jennifer Jooha Lee
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引用次数: 0

Abstract

Background: For patients with ankylosing spondylitis (AS) who experience inefficacy or adverse events with biologics, no recommendations exist regarding the preference for class cycling or switching as a second- or higher-line biologics. Previous studies on the drug retention of TNF and IL-17 inhibitors in AS patients with prior biologics exposure have limitations, including relatively short follow-up periods, exclusion of patients with extra-articular manifestations, and a primary focus on second-line treatment. This study aimed to compare the retention rates of TNF and IL-17 inhibitors in AS patients with prior biologics experience, over a relatively longer follow-up period in real clinical practice.

Methods: A total of 148 AS cases receiving either a TNF or IL-17 inhibitor as a second- or higher-line biologic were retrospectively analyzed after propensity score matching. Patient characteristics at the time of cycling or switching and drug retention were compared between the two groups. Subgroup analyses were conducted based on the reasons for drug discontinuation. Cox regression analyses were used to identify the factors associated with drug discontinuation.

Results: The median follow-up period was 31.4 months, and drug survival tended to be lower for IL-17 inhibitors than for TNF inhibitors in the Kaplan-Meier analysis (P = 0.134). The lower retention of IL-17 inhibitors was more pronounced when discontinuations unrelated to treatment failure were censored (P = 0.034) or when used for reasons other than psoriasis aggravation (P = 0.028). However, in multivariable Cox regression, the number of previous biologics (HR: 1.62, 95% CI: 1.17-2.23, P = 0.003) and BASDAI (HR: 1.3, 95% CI: 1.03-1.65, P = 0.030) were significantly associated with drug discontinuation, whereas the class of biologics did not reach statistical significance (HR: 2.11, 95% CI: 0.96-4.63, P = 0.064).

Conclusion: In patients with AS who had prior experience with biologics, the drug retention of TNF inhibitors tended to be higher compared to IL-17 inhibitors in real-world clinical practice. However, the factors significantly associated with higher drug survival were a lower number of previously exposed biologics and a lower BASDAI.

Abstract Image

Abstract Image

TNF抑制剂与IL-17抑制剂在强直性脊柱炎患者既往生物制剂经验中的保留率
背景:对于使用生物制剂无效或发生不良事件的强直性脊柱炎(AS)患者,没有关于首选分级循环或切换为二线或更高线生物制剂的建议。先前对既往生物制剂暴露的AS患者的TNF和IL-17抑制剂药物保留的研究存在局限性,包括随访时间相对较短,排除了有关节外表现的患者,并且主要关注二线治疗。本研究旨在比较具有生物制剂治疗经验的AS患者在相对较长的临床随访期内TNF和IL-17抑制剂的保留率。方法:在倾向评分匹配后,对148例接受TNF或IL-17抑制剂作为二线或二线生物制剂的AS病例进行回顾性分析。比较两组患者在循环或转换时的特征和药物保留情况。根据停药原因进行亚组分析。采用Cox回归分析确定与停药相关的因素。结果:中位随访期为31.4个月,Kaplan-Meier分析显示,IL-17抑制剂的药物生存期往往低于TNF抑制剂(P = 0.134)。当与治疗失败无关的停药(P = 0.034)或因银屑病加重以外的原因使用时(P = 0.028), IL-17抑制剂的保留率较低更为明显。然而,在多变量Cox回归中,既往生物制剂的数量(HR: 1.62, 95% CI: 1.17-2.23, P = 0.003)和BASDAI (HR: 1.3, 95% CI: 1.03-1.65, P = 0.030)与停药有显著相关,而生物制剂的种类(HR: 2.11, 95% CI: 0.96-4.63, P = 0.064)无统计学意义。结论:在先前使用过生物制剂的AS患者中,在现实世界的临床实践中,TNF抑制剂的药物保留率往往高于IL-17抑制剂。然而,与较高的药物生存期显著相关的因素是先前暴露的生物制剂数量较少和BASDAI较低。
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来源期刊
CiteScore
8.60
自引率
2.00%
发文量
261
审稿时长
14 weeks
期刊介绍: Established in 1999, Arthritis Research and Therapy is an international, open access, peer-reviewed journal, publishing original articles in the area of musculoskeletal research and therapy as well as, reviews, commentaries and reports. A major focus of the journal is on the immunologic processes leading to inflammation, damage and repair as they relate to autoimmune rheumatic and musculoskeletal conditions, and which inform the translation of this knowledge into advances in clinical care. Original basic, translational and clinical research is considered for publication along with results of early and late phase therapeutic trials, especially as they pertain to the underpinning science that informs clinical observations in interventional studies.
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