Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical Practice

Plain Language Summary Rheumatoid arthritis (RA) is a chronic autoimmune disease that can lead to joint damage and disability. The steroid prednisone is a fast-acting and effective treatment for RA and is often prescribed alongside disease-modifying antirheumatic drugs (DMARDs). The health risks ass...

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Main Authors: Dimitrios A. Pappas, Carol J. Etzel, Steve Zlotnick, Jennie Best, Taylor Blachley, Joel M. Kremer
Format: Article
Language:English
Published: Adis, Springer Healthcare 2019-06-01
Series:Rheumatology and Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1007/s40744-019-0162-6
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author Dimitrios A. Pappas
Carol J. Etzel
Steve Zlotnick
Jennie Best
Taylor Blachley
Joel M. Kremer
author_facet Dimitrios A. Pappas
Carol J. Etzel
Steve Zlotnick
Jennie Best
Taylor Blachley
Joel M. Kremer
author_sort Dimitrios A. Pappas
collection DOAJ
description Plain Language Summary Rheumatoid arthritis (RA) is a chronic autoimmune disease that can lead to joint damage and disability. The steroid prednisone is a fast-acting and effective treatment for RA and is often prescribed alongside disease-modifying antirheumatic drugs (DMARDs). The health risks associated with the long-term use of prednisone have led to recommendations to minimize prednisone dose and duration of treatment. Few studies have examined the extent to which biologic DMARDs allow rheumatologists to reduce or discontinue the use of prednisone. The objective of this study was to evaluate changes in prednisone dose while receiving tocilizumab (TCZ) in patients with RA seen in routine US clinical practice. Patients who were enrolled in the Corrona RA registry and were beginning treatment with TCZ were included. Changes in prednisone use were evaluated 12 months after starting treatment. Of patients receiving prednisone at study initiation, 30.6% had discontinued prednisone over 12 months; among patients receiving > 7.5 mg of prednisone at the time of TCZ initiation, 63.0% discontinued prednisone or decreased the dose by ≥ 5 mg over 12 months. In secondary analyses, 29.7% of patients receiving prednisone at study initiation had discontinued prednisone over 6 months; among those receiving > 7.5 mg of prednisone at baseline, 51.3% discontinued or decreased the dose by ≥ 5 mg over 6 months. Changes in prednisone use and improvement in disease activity over 6 and 12 months were comparable between patients who initiated TCZ monotherapy or combination therapy with other DMARDs.
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spelling doaj.art-b8f8960d51e74f3291b1367e51554c6d2022-12-22T01:30:38ZengAdis, Springer HealthcareRheumatology and Therapy2198-65762198-65842019-06-016342143310.1007/s40744-019-0162-6Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical PracticeDimitrios A. Pappas0Carol J. Etzel1Steve Zlotnick2Jennie Best3Taylor Blachley4Joel M. Kremer5Columbia UniversityCorrona, LLCGenentech, IncGenentech, IncCorrona, LLCCorrona, LLCPlain Language Summary Rheumatoid arthritis (RA) is a chronic autoimmune disease that can lead to joint damage and disability. The steroid prednisone is a fast-acting and effective treatment for RA and is often prescribed alongside disease-modifying antirheumatic drugs (DMARDs). The health risks associated with the long-term use of prednisone have led to recommendations to minimize prednisone dose and duration of treatment. Few studies have examined the extent to which biologic DMARDs allow rheumatologists to reduce or discontinue the use of prednisone. The objective of this study was to evaluate changes in prednisone dose while receiving tocilizumab (TCZ) in patients with RA seen in routine US clinical practice. Patients who were enrolled in the Corrona RA registry and were beginning treatment with TCZ were included. Changes in prednisone use were evaluated 12 months after starting treatment. Of patients receiving prednisone at study initiation, 30.6% had discontinued prednisone over 12 months; among patients receiving > 7.5 mg of prednisone at the time of TCZ initiation, 63.0% discontinued prednisone or decreased the dose by ≥ 5 mg over 12 months. In secondary analyses, 29.7% of patients receiving prednisone at study initiation had discontinued prednisone over 6 months; among those receiving > 7.5 mg of prednisone at baseline, 51.3% discontinued or decreased the dose by ≥ 5 mg over 6 months. Changes in prednisone use and improvement in disease activity over 6 and 12 months were comparable between patients who initiated TCZ monotherapy or combination therapy with other DMARDs.http://link.springer.com/article/10.1007/s40744-019-0162-6PrednisoneRegistryRheumatoid arthritisTocilizumab
spellingShingle Dimitrios A. Pappas
Carol J. Etzel
Steve Zlotnick
Jennie Best
Taylor Blachley
Joel M. Kremer
Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical Practice
Rheumatology and Therapy
Prednisone
Registry
Rheumatoid arthritis
Tocilizumab
title Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical Practice
title_full Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical Practice
title_fullStr Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical Practice
title_full_unstemmed Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical Practice
title_short Patterns of Prednisone Use in Patients with Rheumatoid Arthritis Initiating Treatment with Tocilizumab in Routine US Clinical Practice
title_sort patterns of prednisone use in patients with rheumatoid arthritis initiating treatment with tocilizumab in routine us clinical practice
topic Prednisone
Registry
Rheumatoid arthritis
Tocilizumab
url http://link.springer.com/article/10.1007/s40744-019-0162-6
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