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Review
. 2018 Aug 20:9:275-284.
doi: 10.2147/PROM.S147286. eCollection 2018.

Sarilumab: patient-reported outcomes in rheumatoid arthritis

Affiliations
Review

Sarilumab: patient-reported outcomes in rheumatoid arthritis

Chiara Crotti et al. Patient Relat Outcome Meas. .

Abstract

In the last few decades, strategies for the management of rheumatoid arthritis (RA) have been increasingly oriented toward more comprehensive control of the disease, taking into account even RA extra-articular manifestations, comorbidities, and the patient's perception about the disease. The need for improving the shared decision-making process suggested by European League Against Rheumatism recommendations is leading to an increasing interest in the role of patient-reported outcomes (PROs) beside the usual more objective criteria for defining clinical response based on disease-activity composite indices. Measurement of such PROs as pain or fatigue may be significantly influenced by mood disorders often complicating RA, the pathogenesis of which is deeply interconnected with phlogistic processes mediated by proinflammatory cytokines. IL6 is a pleiotropic mediator involved in neuroendocrine and neuropsychological processes, besides its well known effects on immune, cardiovascular, and metabolic systems. Therefore, there is a growing body of evidence about the efficacy of IL6 blockade in PRO improvement in RA patients. Sarilumab is a monoclonal antibody binding both soluble and membrane-bound IL6Rα, inhibiting the IL6-mediated signaling pathway with favorable efficacy and safety profile. This review analyzes the importance of PROs in strategies for the management of RA and the pathogenic mechanisms linking IL6 with the patient's perception of the disease. Moreover, the main findings from sarilumab randomized controlled trials are summarized in detail, emphasizing the potential role of this IL6 blocker in the holistic treatment of RA.

Keywords: interleukin-6; patient reported outcome; rheumatoid arthritis; sarilumab.

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Conflict of interest statement

Disclosure EGF has received lecture fees from BMS, Roche, MSD, UCB, Pfizer, and AbbVie. The authors report no other conflicts of interest in this work.

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