对长期接受 TNF-α 抑制剂治疗的类风湿关节炎患者的疾病活动进行为期 48 个月的监测:临床结果预测时间以及生物仿制药与生物原研药的性能对比。

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2024-03-01 Epub Date: 2024-01-31 DOI:10.1007/s40261-024-01341-7
Matteo Colina, Micheline Khodeir, Roberto Rimondini, Marco Valentini, Federica Campomori, Stefania Corvaglia, Gabriele Campana
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引用次数: 0

摘要

背景和目的:肿瘤坏死因子-α抑制剂对类风湿性关节炎患者的长期治疗会导致疾病活动的初步变化,而这种变化可以预测后期的治疗反应。这项观察性和回顾性研究旨在确定,在类风湿关节炎久治不愈的情况下,何时可以预测治疗反应,同时比较原始生物制剂和生物仿制药的疗效:共招募了1598名患者,他们接受了原生物制剂阿达木单抗和依那西普或生物仿制药的治疗。对患者进行了为期48个月的监测,每6个月测量一次疾病活动评分(28关节疾病活动评分、简化疾病活动指数和临床疾病活动指数):在依那西普与生物仿制药(GP2015/SB4)以及阿达木单抗与生物仿制药(GP2017)患者组中,未观察到疾病活动水平的差异。在治疗的前18个月中,所有治疗方法的所有评分都明显下降,24个月后达到最低值,并持续48个月:我们得出的结论是,阿达木单抗和依那西普的生物仿制药与其原研药相比具有同等的长期疗效,而且使用肿瘤坏死因子-α抑制剂(原研药和生物仿制药)6个月后的疾病活动水平可以预测长期类风湿关节炎患者4年后的治疗反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Forty-Eight-Month Monitoring of Disease Activity in Patients with Long-Standing Rheumatoid Arthritis Treated with TNF-α Inhibitors: Time for Clinical Outcome Prediction and Biosimilar vs Biologic Originator Performance.

Forty-Eight-Month Monitoring of Disease Activity in Patients with Long-Standing Rheumatoid Arthritis Treated with TNF-α Inhibitors: Time for Clinical Outcome Prediction and Biosimilar vs Biologic Originator Performance.

Background and objectives: Long-term treatment of patients with rheumatoid arthritis with tumor necrosis factor-α inhibitors leads to initial changes in disease activity that can predict a late treatment response. This observational and retrospective study aimed to determine when it is possible to foresee the response to therapy in the case of long-standing rheumatoid arthritis comparing also the efficacy of the original biologics with their biosimilars.

Methods: A total of 1598 patients were recruited and treated with the original biologics, adalimumab and etanercept, or with biosimilars. Patients were monitored over a period of 48 months and disease activity scores (28-Joint Disease Activity Score, Simplified Disease Activity Index, and Clinical Disease Activity Index) were measured every 6 months.

Results: No differences in disease activity levels were observed in etanercept versus biosimilars (GP2015/SB4) and adalimumab versus biosimilar (GP2017) patient groups. All scores significantly decreased in all treatments during the first 18 months of therapy, and after 24 months reached a minimum that lasted up to 48 months.

Conclusions: We conclude that biosimilars of adalimumab and etanercept have equivalent effectiveness over a long period of time compared to their originator drugs, and also that the levels of disease activity after 6 months of tumor necrosis factor-α inhibitors (originator drugs and biosimilars) might predict the response to therapy at 4 years in patients with long-standing rheumatoid arthritis.

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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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