Factors Influencing Selection of First Add-on Disease-Modifying Therapy for Rheumatoid Arthritis after Starting Methotrexate

Author(s)

Huang Y1, Agarwal S2, Chen H3, Johnson ML3, Chatterjee S4, Aparasu RR3
1University of Houston, College of Pharmacy, houston, TX, USA, 2Baylor College of Medicine, Houston, TX, USA, 3University of Houston, College of Pharmacy, Houston, TX, USA, 4Boehringer-Ingelheim, Ridgefield, CT, USA

OBJECTIVES: Disease-modifying anti-rheumatic drugs (DMARD) are often added to methotrexate (MTX) for managing rheumatoid arthritis (RA). This study examined the factors associated with the first add-on DMARD for RA patients receiving MTX.

METHODS: This retrospective cohort study involved DMARD-naïve patients aged ≥18 with RA initiating MTX (index date) between July 1st 2012-Dec 30th 2013, from the MarketScan Claims data. Patients had continuous enrollment for the 6-month pre-index period, and the addition of conventional synthetic (cs) DMARDs, tumor necrosis factor inhibitors (TNFi), biological (b) DMARDs, or non-TNFi bDMARDs was assessed during 1-year post-index period. Combination therapy was defined as having an MTX prescription within the first 30 days after DMARD initiation. A multivariable logistic regression analysis was used to examine the factors associated with the addition of TNFi versus csDMARD. A second multivariable regression evaluated the factors associated with adding any biologics by combining TNFi and non-TNF biologics to bDMARD.

RESULTS: Among 2,665 DMARD-naïve RA patients initiating MTX, majority were added TNFi (550 (58%)), followed by csDMARD (352 (37%)) and non-TNF biologics (40 (4%)). Most of the patients receiving combination therapy were females (79%), from South (46%), and with preferred provider organization (PPO) plan (64.%). Enabling factors of PPO (odds ratio (OR) [95% confidence interval (CI)], 1.40 [1.03-1.89]), need factors of chronic pulmonary disease (1.73[1.02-2.96]), liver disease (4.11 [1.46-11.61]), glucocorticoid injection (1.44 [1.03-2.01]), human leukocyte antigen gene test (1.61 [1.01-2.56]), Elixhauser index (0.93 [0.88-0.98]) and antibodies to mutated citrullinated vimentin test (0.54 [0.30-0.99]) were associated with adding a TNFi. The second model additionally found that enabling factor of metropolitan statistical area (1.49 [1.03-2.16]) was associated with adding any biologics.

CONCLUSIONS: TNFi are often added to MTX regimen for the management of RA. Both enabling and need factors were associated with the addition of TNFi to MTX therapy for managing RA.

Conference/Value in Health Info

2022-05, ISPOR 2022, Washington, DC, USA

Value in Health, Volume 25, Issue 6, S1 (June 2022)

Code

HSD133

Topic

Epidemiology & Public Health, Study Approaches

Topic Subcategory

Safety & Pharmacoepidemiology

Disease

Musculoskeletal Disorders

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