Biologic and Glucocorticoid Use after Methotrexate Initiation in Patients with Rheumatoid Arthritis

Objective. Biologic therapies can improve disease control for patients with rheumatoid arthritis (RA) but may be both overused and underused. We aimed to identify predictors of greater use of biologic therapies and to identify factors associated with persistent glucocorticoid use. Methods. Using national US Veteran’s Affairs databases 2005–2016, we identified patients with RA receiving a first-ever prescription of methotrexate (MTX), requiring ≥ 6 months of baseline data. We evaluated predictors of biologic therapy initiation within 2 years of starting MTX and factors associated with baseline and persistent glucocorticoid use at 6–12 months using multivariable models. Results. Among 17,415 patients starting MTX, 3263 patients received biologic therapy within 2 years (20.6% 2-yr incidence). In adjusted analyses, biologic use was substantially lower in older patients [e.g., aHR 0.20 (95% CI 0.16, 0.26) for patients ≥ 80 vs < 50] and patients with more comorbidities [aHR 0.79 (95% CI 0.72, 0.87) for Charlson score ≥ 3 vs < 3]. Patients with heart failure [aHR 0.68 (95% CI 0.54, 0.84)], cancer [aHR 0.78 (95% CI 0.66, 0.92)], or who were nonwhite [aHR 0.79 (95% CI 0.72, 0.87)] were also less likely to receive a biologic. In contrast, baseline and persistent glucocorticoid use was similar across age groups and more common in patients with greater comorbidity. Conclusion. Biologic therapy is initiated less frequently in patients with RA who are older, have more comorbidities, and who are nonwhite. While biologics may be avoided in older and sicker patients because of safety concerns, glucocorticoid use is similar regardless of age and is more frequent in patients with comorbidities, with implications for patient outcomes.

[1]  C. Spivey,et al.  A Retrospective Analysis of Corticosteroid Utilization Before Initiation of Biologic DMARDs Among Patients with Rheumatoid Arthritis in the United States , 2018, Rheumatology and Therapy.

[2]  J. O'dell,et al.  It is the Best of Treatments, It is the Worst of Treatments: The Continuing Love‐Hate Relationship With Glucocorticoids in Rheumatoid Arthritis , 2017, Arthritis care & research.

[3]  R. Desai,et al.  Factors associated with initial or subsequent choice of biologic disease-modifying antirheumatic drugs for treatment of rheumatoid arthritis , 2017, Arthritis Research & Therapy.

[4]  H. Sayles,et al.  Utilization of Care Outside the Veterans Affairs Health Care System by US Veterans With Rheumatoid Arthritis , 2017, Arthritis care & research.

[5]  T. Mikuls,et al.  Persistence With Conventional Triple Therapy Versus a Tumor Necrosis Factor Inhibitor and Methotrexate in US Veterans With Rheumatoid Arthritis , 2017, Arthritis care & research.

[6]  R. Sruamsiri,et al.  Treatment patterns of rheumatoid arthritis in Japanese hospitals and predictors of the initiation of biologic agents , 2017, Current medical research and opinion.

[7]  K. Michaud,et al.  Changes in Body Mass Related to the Initiation of Disease‐Modifying Therapies in Rheumatoid Arthritis , 2016, Arthritis & rheumatology.

[8]  Charles King,et al.  2015 American College of Rheumatology Guideline for the Treatment of Rheumatoid Arthritis , 2016, Arthritis & rheumatology.

[9]  K. Roback,et al.  Physician Preferences and Variations in Prescription of Biologic Drugs for Rheumatoid Arthritis: A Register‐Based Study of 4,010 Patients in Sweden , 2015, Arthritis care & research.

[10]  M. Dougados,et al.  Treatment Patterns of Multimorbid Patients with Rheumatoid Arthritis: Results from an International Cross-sectional Study , 2015, The Journal of Rheumatology.

[11]  R. Hansen,et al.  Predictors of Treatment Initiation with Tumor Necrosis Factor-α Inhibitors in Patients with Rheumatoid Arthritis , 2014, Journal of managed care & specialty pharmacy.

[12]  K. Rascati,et al.  Factors Associated With The Initiation Of Biologic Disease Modifying Antirheumatic Drugs In Texas Medicaid Patients With Rheumatoid Arthritis , 2014 .

[13]  Z. Mulla,et al.  Concomitant chronic pulmonary diseases and their association with hospital outcomes in patients with anaphylaxis and other allergic conditions: a cohort study , 2013, BMJ Open.

[14]  R. Caporali,et al.  The role of low-dose glucocorticoids for rheumatoid arthritis in the biologic era. , 2013, Clinical and experimental rheumatology.

[15]  B. Ng,et al.  Factors associated with methotrexate dosing and therapeutic decisions in veterans with rheumatoid arthritis , 2013, Clinical Rheumatology.

[16]  A. Reimold,et al.  Merging Veterans Affairs rheumatoid arthritis registry and pharmacy data to assess methotrexate adherence and disease activity in clinical practice , 2011, Arthritis care & research.

[17]  W. Dixon,et al.  The association between systemic glucocorticoid therapy and the risk of infection in patients with rheumatoid arthritis: systematic review and meta-analyses , 2011, Arthritis research & therapy.

[18]  Sebastian Schneeweiss,et al.  A combined comorbidity score predicted mortality in elderly patients better than existing scores. , 2011, Journal of clinical epidemiology.

[19]  Jeffrey N Katz,et al.  Validation of rheumatoid arthritis diagnoses in health care utilization data , 2011, Arthritis research & therapy.

[20]  Tsutomu Takeuchi,et al.  EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2016 update , 2010, Annals of the rheumatic diseases.

[21]  John Wong,et al.  EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs , 2010, Annals of the rheumatic diseases.

[22]  D. Solomon,et al.  Physician preference motivates the use of anti–tumor necrosis factor therapy independent of clinical disease activity , 2010, Arthritis care & research.

[23]  K. Anstrom,et al.  Pattern and predictors of the initiation of biologic agents for the treatment of rheumatoid arthritis in the United States: an analysis using a large observational data bank. , 2009, Clinical therapeutics.

[24]  H. Quan,et al.  Coding Algorithms for Defining Comorbidities in ICD-9-CM and ICD-10 Administrative Data , 2005, Medical care.

[25]  B. Gage,et al.  Accuracy of ICD-9-CM Codes for Identifying Cardiovascular and Stroke Risk Factors , 2005, Medical care.

[26]  T. Mikuls,et al.  Use of Biologic Therapy in Racial Minorities With Rheumatoid Arthritis From 2 US Health Care Systems , 2017, Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases.

[27]  Raveendhara R. Bannuru,et al.  American College of Rheumatology Guideline for the Treatment of Rheumatoid Arthritis , 2015 .

[28]  J. Listing,et al.  The risk of infections associated with rheumatoid arthritis, with its comorbidity and treatment. , 2013, Rheumatology.

[29]  Mary K Goldstein,et al.  Accuracy of computerized outpatient diagnoses in a Veterans Affairs general medicine clinic. , 2002, The American journal of managed care.