• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

生物类似药治疗类风湿关节炎的历程:通过节省成本和预防反安慰剂效应,实现更好的可及性和良好的疾病控制。

Treatment journey in rheumatoid arthritis with biosimilars: from better access to good disease control through cost savings and prevention of nocebo effects.

机构信息

Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria

Division of Clinical Rheumatology, ASST Gaetano Pini-CTO Institute, Milano, Italy.

出版信息

RMD Open. 2021 Jun;7(2). doi: 10.1136/rmdopen-2021-001637.

DOI:10.1136/rmdopen-2021-001637
PMID:34099538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8186742/
Abstract

Early diagnosis and treatment of rheumatoid arthritis (RA) are of critical importance to halt the progression of the disease. Optimal use of advanced imaging techniques or biomarkers may facilitate early diagnosis of RA. Even though many disease-modifying anti-rheumatic drugs (DMARDs) are available for RA treatment, biological DMARDs (bDMARDs) offer expanding therapeutic options and good outcomes in patients with RA who do not have a sufficient response to conventional synthetic DMARDs. However, high costs of bDMARDs have limited patient access to optimised disease management and increased the cost burden for healthcare systems. The advent of biosimilars led to significant cost savings driven by price competition among the reference products, which could be beneficial for healthcare systems. Healthcare provider (HCP)-patient communication and informed shared decision-making are crucial to prevent the occurrence of a nocebo effect, which results from negative perceptions that patients may have and could lead to less effective outcomes. Research has demonstrated that effective communication between HCPs and patients utilising positive framing can improve acceptance by patients to be initiated on or switched to a biosimilar and can help to integrate biosimilars into routine clinical practice to maximise benefits for patients with RA.

摘要

类风湿关节炎(RA)的早期诊断和治疗对阻止疾病进展至关重要。优化使用先进的影像学技术或生物标志物可能有助于早期诊断 RA。尽管有许多治疗类风湿关节炎的疾病修饰抗风湿药物(DMARDs),但生物 DMARDs(bDMARDs)为对传统合成 DMARDs 反应不足的 RA 患者提供了更多的治疗选择和良好的疗效。然而,bDMARDs 的高成本限制了患者获得优化疾病管理的机会,并增加了医疗保健系统的成本负担。生物类似药的出现带来了显著的成本节约,这是由于参考产品之间的价格竞争所致,这对医疗保健系统可能是有益的。医疗保健提供者(HCP)与患者之间的沟通和知情的共同决策对于预防出现源自于患者负面看法的“反安慰剂效应”至关重要,这可能导致治疗效果不佳。研究表明,HCP 与患者之间使用积极框架的有效沟通可以提高患者对生物类似药的接受度,使其开始使用或转换为生物类似药,并有助于将生物类似药纳入常规临床实践,从而使 RA 患者最大程度受益。

相似文献

1
Treatment journey in rheumatoid arthritis with biosimilars: from better access to good disease control through cost savings and prevention of nocebo effects.生物类似药治疗类风湿关节炎的历程:通过节省成本和预防反安慰剂效应,实现更好的可及性和良好的疾病控制。
RMD Open. 2021 Jun;7(2). doi: 10.1136/rmdopen-2021-001637.
2
Era of biosimilars in rheumatology: reshaping the healthcare environment.生物类似药时代:重塑医疗保健环境。
RMD Open. 2019 May 21;5(1):e000900. doi: 10.1136/rmdopen-2019-000900. eCollection 2019.
3
Budget Impact of Sequential Treatment with Biologics, Biosimilars, and Targeted Synthetic Disease-Modifying Antirheumatic Drugs in Thai Patients with Rheumatoid Arthritis.生物制剂、生物类似药和靶向合成疾病修正抗风湿药物序贯治疗对泰国类风湿关节炎患者的预算影响。
Adv Ther. 2021 Sep;38(9):4885-4899. doi: 10.1007/s12325-021-01867-8. Epub 2021 Aug 9.
4
The safety of emerging biosimilar drugs for the treatment of rheumatoid arthritis.用于治疗类风湿性关节炎的新型生物类似药的安全性。
Expert Opin Drug Saf. 2017 Mar;16(3):289-302. doi: 10.1080/14740338.2017.1273899. Epub 2017 Jan 10.
5
Factors influencing clinician prescribing of disease-modifying anti-rheumatic drugs for inflammatory arthritis: A systematic review and thematic synthesis of qualitative studies.影响临床医生为炎症性关节炎开具疾病修正抗风湿药物的因素:系统评价和定性研究的主题综合分析。
Semin Arthritis Rheum. 2022 Aug;55:151988. doi: 10.1016/j.semarthrit.2022.151988. Epub 2022 Feb 27.
6
Biosimilars for the management of rheumatoid arthritis: economic considerations.用于类风湿性关节炎治疗的生物类似药:经济考量
Expert Rev Clin Immunol. 2015;11 Suppl 1:S43-52. doi: 10.1586/1744666X.2015.1090313.
7
The nocebo effect challenges the non-medical infliximab switch in practice.在实际应用中,反安慰剂效应给英夫利昔单抗的非医学转换带来了挑战。
Eur J Clin Pharmacol. 2018 May;74(5):655-661. doi: 10.1007/s00228-018-2418-4. Epub 2018 Jan 24.
8
Impact of Infliximab and Etanercept Biosimilars on Biological Disease-Modifying Antirheumatic Drugs Utilisation and NHS Budget in the UK.英夫利昔单抗和依那西普生物类似药对英国生物改善型抗风湿药物利用和 NHS 预算的影响。
BioDrugs. 2017 Dec;31(6):533-544. doi: 10.1007/s40259-017-0252-3.
9
To See or NOsee: The Debate on the Nocebo Effect and Optimizing the Use of Biosimilars.见或不见:关于非安慰剂效应的争论和优化生物类似药的使用。
Adv Ther. 2018 Jun;35(6):749-753. doi: 10.1007/s12325-018-0719-8. Epub 2018 Jun 5.
10
Biologic Drugs for Rheumatoid Arthritis in the Context of Biosimilars, Genetics, Epigenetics and COVID-19 Treatment.生物类似药背景下治疗类风湿关节炎的生物制剂、遗传学、表观遗传学与 COVID-19 治疗
Cells. 2021 Feb 4;10(2):323. doi: 10.3390/cells10020323.

引用本文的文献

1
Comparative effectiveness and safety of biosimilars versus reference biologics in rheumatoid arthritis during treatment initiation: a systematic review of real-world evidence.生物类似药与参照生物制品在类风湿关节炎治疗起始阶段的比较有效性和安全性:真实世界证据的系统评价
Int J Clin Pharm. 2025 Jun 25. doi: 10.1007/s11096-025-01956-6.
2
From Conventional to Advanced Therapies: A National Health Registry Report (2016-2022) on DMARDs in Rheumatoid Arthritis Treatment in Turkey.从传统疗法到先进疗法:土耳其类风湿关节炎治疗中改善病情抗风湿药的国家健康注册报告(2016 - 2022年)
Biologics. 2025 May 26;19:331-339. doi: 10.2147/BTT.S507132. eCollection 2025.
3

本文引用的文献

1
The switch from etanercept originator to SB4: data from a real-life experience on tolerability and persistence on treatment in joint inflammatory diseases.从原研依那西普转换为SB4:来自关节炎症性疾病治疗耐受性和持续性真实生活经验的数据。
Ther Adv Musculoskelet Dis. 2020 Oct 13;12:1759720X20964031. doi: 10.1177/1759720X20964031. eCollection 2020.
2
Physicians' perceptions of the uptake of biosimilars: a systematic review.医生对生物类似药采用情况的看法:系统评价。
BMJ Open. 2020 May 5;10(5):e034183. doi: 10.1136/bmjopen-2019-034183.
3
Shift From Adalimumab Originator to Biosimilars in Denmark.
Global, regional and national trends in the epidemiology of rheumatoid arthritis from 1990 to 2021: an age-period-cohort effect analysis of the global burden of disease study 2021.
1990年至2021年类风湿关节炎流行病学的全球、区域和国家趋势:2021年全球疾病负担研究的年龄-时期-队列效应分析
RMD Open. 2025 Apr 12;11(2):e005383. doi: 10.1136/rmdopen-2024-005383.
4
Efficacy, Safety, and Immunogenicity of Biosimilar Adalimumab Advixa® Compared With Reference Product Humira® in Patients With Rheumatoid Arthritis in Bangladesh.在孟加拉国类风湿关节炎患者中,生物类似药阿达木单抗Advixa®与参比产品修美乐®相比的疗效、安全性及免疫原性
Cureus. 2025 Jan 18;17(1):e77638. doi: 10.7759/cureus.77638. eCollection 2025 Jan.
5
Cost-consequence analysis of early vs. delayed natalizumab use in highly active relapsing-remitting multiple sclerosis: a simulation study. natalizumab早期使用与延迟使用在高度活动性复发缓解型多发性硬化症中的成本-后果分析:一项模拟研究
J Neurol. 2025 Jan 17;272(2):153. doi: 10.1007/s00415-024-12723-4.
6
Biosimilars for Rheumatoid Arthritis: Riding the 2023 Wave [Podcast].类风湿关节炎生物类似药:乘上2023年的浪潮 [播客]
Open Access Rheumatol. 2023 Oct 31;15:207-212. doi: 10.2147/OARRR.S443235. eCollection 2023.
7
Switching from One Biosimilar to Another Biosimilar of the Same Reference Biologic: A Systematic Review of Studies.从一种生物类似药切换至同一种参照生物制品的另一种生物类似药:研究的系统评价。
BioDrugs. 2022 Sep;36(5):625-637. doi: 10.1007/s40259-022-00546-6. Epub 2022 Jul 26.
8
Big data analyses and individual health profiling in the arena of rheumatic and musculoskeletal diseases (RMDs).风湿性和肌肉骨骼疾病(RMDs)领域的大数据分析与个人健康档案
Ther Adv Musculoskelet Dis. 2022 Jun 30;14:1759720X221105978. doi: 10.1177/1759720X221105978. eCollection 2022.
9
Factors affecting patient satisfaction related to cost and treatment effectiveness in rheumatoid arthritis: results from the multicenter observational cohort study, FRANK Registry.影响类风湿关节炎患者对成本和治疗效果满意度的因素:来自多中心观察性队列研究 FRANK 注册表的结果。
Arthritis Res Ther. 2022 Feb 22;24(1):53. doi: 10.1186/s13075-022-02746-5.
丹麦阿达木单抗由原研药转为生物类似药。
JAMA Intern Med. 2020 Jun 1;180(6):902-903. doi: 10.1001/jamainternmed.2020.0338.
4
The Future of Biosimilars: Maximizing Benefits Across Immune-Mediated Inflammatory Diseases.生物类似药的未来:最大限度地提高免疫介导的炎症性疾病的获益。
Drugs. 2020 Feb;80(2):99-113. doi: 10.1007/s40265-020-01256-5.
5
EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update.EULAR 推荐的类风湿关节炎治疗策略:2019 年更新版(使用合成和生物疾病修正抗风湿药物)
Ann Rheum Dis. 2020 Jun;79(6):685-699. doi: 10.1136/annrheumdis-2019-216655. Epub 2020 Jan 22.
6
Identifying Key Benefits in European Off-Patent Biologics and Biosimilar Markets: It is Not Only About Price!识别欧洲非专利生物制品和生物类似药市场的关键优势:不仅仅是价格!
BioDrugs. 2020 Apr;34(2):159-170. doi: 10.1007/s40259-019-00395-w.
7
The Danish model for the quick and safe implementation of infliximab and etanercept biosimilars.丹麦快速安全实施英夫利昔单抗和依那西普生物类似药的模式。
Eur J Clin Pharmacol. 2020 Jan;76(1):35-40. doi: 10.1007/s00228-019-02765-3. Epub 2019 Nov 1.
8
Does a mandatory non-medical switch from originator to biosimilar etanercept lead to increase in healthcare use and costs? A Danish register-based study of patients with inflammatory arthritis.从原研药到生物类似药依那西普的强制性非医学转换是否会导致炎症性关节炎患者的医疗保健使用和成本增加?一项丹麦基于登记的研究。
RMD Open. 2019 Aug 12;5(2):e001016. doi: 10.1136/rmdopen-2019-001016. eCollection 2019.
9
The 4-H of Biomarkers in Arthritis: A Lot of Help, Occasional Harm, Some Hype, Increasing Hope.关节炎生物标志物的 4-H:很多帮助,偶尔的危害,一些炒作,越来越有希望。
J Rheumatol. 2019 Jul;46(7):758-763. doi: 10.3899/jrheum.190375.
10
Are we ready to close the discussion on the interchangeability of biosimilars?我们是否已经准备好结束关于生物类似药可互换性的讨论?
Drug Discov Today. 2019 Oct;24(10):1963-1967. doi: 10.1016/j.drudis.2019.06.016. Epub 2019 Jun 26.