Abstract

BackgroundSince persistence to first biological disease modifying anti-rheumatic drugs (bDMARDs) is far from ideal in rheumatoid arthritis (RA) patients, many do receive a second and/or third bDMARD treatment. However, little is known about treatment persistence of the second-line bDMARD and it is specifically unknown whether the mode of action of such a treatment is associated with different persistence rates. We aimed to assess discontinuation-, re-initiation- or continuation-rates of a 2nd bDMARD therapy as well as switching-rates to a third biological DMARD (3rd bDMARD) therapy in RA patients.MethodAnalysis was based on German claims data (2010–2013). Patients were included if they had received at least one prescription for an anti-TNF and at least one follow-up prescription of a 2nd bDMARD different from the first anti-TNF. Patient follow-up started on the date of the first prescription for the 2nd bDMARD and lasted for 12 months or until a patient’s death.Results2667 RA patients received at least one anti-TNF prescription. Of these, 451 patients received a second bDMARD (340 anti-TNF, mean age 52.6 years; 111 non-anti-TNF, mean age 55.9 years).During the follow-up, 28.8% vs. 11.7% of the 2nd anti-TNF vs. non-anti-TNF patients (p < 0.001) switched to a 3rd bDMARD; 14.1% vs. 19.8% (p = 0.179) discontinued without re-start; 3.8% vs.1.8% (p = 0.387) re-started and 53.5 vs. 66.7% (p < 0.050) continued therapy. Patients in the non-anti-TNF group demonstrated longer drug survival (295 days) than patients in the anti-TNF group (264 days; p = 0.016).Independent variables associated with earlier discontinuation (including re-start) or switch were prescription of an anti-TNF as 2nd bDMARD (HR = 1.512) and a higher comorbidity level (CCI, HR = 1.112), whereas previous painkiller medication (HR = 0.629) was associated with later discontinuation or switch.ConclusionsOnly 56.8% of RA patients continued 2nd bDMARD treatment after 12 months; 60% if re-start was included. Non-anti-TNF patients had a higher probability of continuing 2nd bDMARD therapy.

Highlights

  • Since persistence to first biological disease modifying anti-rheumatic drugs is far from ideal in rheumatoid arthritis (RA) patients, many do receive a second and/or third biological DMARD (bDMARD) treatment

  • Independent variables associated with earlier discontinuation or switch were prescription of an anti-Tumour necrosis factor-alpha (TNF) as 2nd bDMARD (HR = 1.512) and a higher comorbidity level (CCI, hazard ratio (HR) = 1.112), whereas previous painkiller medication (HR = 0.629) was associated with later discontinuation or switch

  • Non-anti-TNF patients had a higher probability of continuing 2nd bDMARD therapy

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Summary

Introduction

Since persistence to first biological disease modifying anti-rheumatic drugs (bDMARDs) is far from ideal in rheumatoid arthritis (RA) patients, many do receive a second and/or third bDMARD treatment. We aimed to assess discontinuation-, re-initiation- or continuation-rates of a 2nd bDMARD therapy as well as switching-rates to a third biological DMARD (3rd bDMARD) therapy in RA patients. Current treatment guidelines recommend methotrexate (MTX), a synthetic disease-modifying anti-rheumatic drug (sDMARD), in combination with glucocorticoids to be administered for most newly diagnosed RA patients [5, 6]. If MTX therapy fails to improve symptoms or fails to reach the treatment target, it is recommended to switch to another sDMARD (e.g., sulfasalazine, leflunomide, hydroxychloroquine) or to add a biological DMARD (bDMARD) to MTX therapy. A previous study showed that a substantial proportion of patients receives further lines of biologic treatment after such a discontinuation [15]

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