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“难治性”类风湿关节炎:当前的立场和下一步的考虑。

'Difficult to treat' rheumatoid arthritis: current position and considerations for next steps.

机构信息

Kellgren centre for Rheumatology, Manchester University NHS Foundation Trust, Manchester, UK.

Centre for Musculoskeletal Research, School of Biological Sciences, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK

出版信息

RMD Open. 2022 Jul;8(2). doi: 10.1136/rmdopen-2022-002387.

Abstract

The European Alliance of Associations for Rheumatology recently defined difficult to treat (D2T) rheumatoid arthritis (RA) and provided points to consider in its management. This review summarises the key concepts of D2T-RA that underpinned this recent guidance. D2T-RA is primarily characterised by failure of at least two different mechanism of action biologic/targeted synthetic disease-modifying antirheumatic drug (DMARDs) with evidence of active/progressive disease. The basis for progressive disease, however, is not limited to clear inflammatory joint pathology, capturing wider contributors to treatment cycling such as comorbidity, obesity and fibromyalgia. This means D2T-RA comprises a heterogeneous population, with a proportion within this exhibiting bona fide treatment-refractory disease. The management points to consider, however, emphasise the importance of checking for the presence of inflammatory pathology before further treatment change. This review suggests additional considerations in the definition of D2T-RA, the potential value in identifying D2T traits and intervening before the development of D2T-RA state and the need for real world evidence of targeted synthetic DMARD in this population to compare to recent trial data. Finally, the review asks whether the presence of D2T-RA implies a failure to treat effectively from the outset, and the need for pharmacological and non-pharmacological management approaches to address the wider D2T-RA population effectively.

摘要

欧洲风湿病协会联盟最近定义了难治性(D2T)类风湿关节炎(RA),并提供了在其管理中需要考虑的要点。这篇综述总结了最近这一指南所依据的 D2T-RA 的关键概念。D2T-RA 的主要特征是至少两种不同作用机制的生物/靶向合成疾病修饰抗风湿药物(DMARDs)治疗失败,且有疾病活动/进展的证据。然而,进展性疾病的基础不仅限于明确的炎症性关节病理学,还包括治疗循环中更广泛的促成因素,如合并症、肥胖和纤维肌痛。这意味着 D2T-RA 包含一个异质人群,其中一部分表现出真正的治疗抵抗性疾病。然而,需要考虑的管理要点强调了在进一步治疗改变之前检查是否存在炎症性病理的重要性。这篇综述提出了 D2T-RA 定义中的其他考虑因素,在 D2T-RA 状态出现之前识别 D2T 特征并进行干预的潜在价值,以及在这一人群中需要靶向合成 DMARD 的真实世界证据,以与最近的试验数据进行比较。最后,这篇综述询问 D2T-RA 的存在是否意味着从一开始就未能有效治疗,以及是否需要药理学和非药理学管理方法来有效治疗更广泛的 D2T-RA 人群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b208/9335059/f4ee410fde53/rmdopen-2022-002387f01.jpg

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