Mechanisms underlying DMARD inefficacy in difficult-to-treat rheumatoid arthritis: a narrative review with systematic literature search

Author:

Roodenrijs Nadia M T1ORCID,Welsing Paco M J1,van Roon Joël1,Schoneveld Jan L M2,van der Goes Marlies C13,Nagy György45,Townsend Michael J6,van Laar Jacob M1ORCID

Affiliation:

1. Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht University , Utrecht

2. Department of Rheumatology, Bravis Hospital , Roosendaal

3. Department of Rheumatology, Meander Medical Center , Amersfoort, The Netherlands

4. Department of Rheumatology & Clinical Immunology

5. Department of Genetics, Cell and Immunobiology, Semmelweis University , Budapest, Hungary

6. Biomarker Discovery OMNI, Genentech Research & Early Development , South San Francisco, CA, USA

Abstract

Abstract Management of RA patients has significantly improved over the past decades. However, a substantial proportion of patients is difficult-to-treat (D2T), remaining symptomatic after failing biological and/or targeted synthetic DMARDs. Multiple factors can contribute to D2T RA, including treatment non-adherence, comorbidities and co-existing mimicking diseases (e.g. fibromyalgia). Additionally, currently available biological and/or targeted synthetic DMARDs may be truly ineffective (‘true’ refractory RA) and/or lead to unacceptable side effects. In this narrative review based on a systematic literature search, an overview of underlying (immune) mechanisms is presented. Potential scenarios are discussed including the influence of different levels of gene expression and clinical characteristics. Although the exact underlying mechanisms remain largely unknown, the heterogeneity between individual patients supports the assumption that D2T RA is a syndrome involving different pathogenic mechanisms.

Funder

AbbVie

Pfizer

Astra Zeneca

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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