Literature DB >> 31787605

Reasons for Biologic and Targeted Synthetic Disease-modifying Antirheumatic Drug Cessation and Persistence of Second-line Treatment in a Rheumatoid Arthritis Dataset.

Peter Youssef1, Bruno Marcal1, Peter Button1, Matt Truman1, Paul Bird1, Hedley Griffiths1, Lynden Roberts1, Kathleen Tymms1, Geoff Littlejohn1.   

Abstract

OBJECTIVE: To provide real-world evidence about the reasons why Australian rheumatologists cease biologic (b) and targeted synthetic (ts) disease-modifying antirheumatic drugs (DMARD) when treating patients with rheumatoid arthritis (RA), and to assess (1) the primary failure rate for first-line treatment, and (2) the persistence on second-line treatments in patients who stopped first-line tumor necrosis factor inhibitors (TNFi).
METHODS: This is a multicenter retrospective, noninterventional study of patients with RA enrolled in the Australian Optimising Patient outcome in Australian RheumatoLogy (OPAL) dataset with a start date of b/tsDMARD between August 1, 2010, and June 30, 2017. Primary failure was defined as stopping treatment within 6 months of treatment initiation.
RESULTS: Data from 7740 patients were analyzed; 6914 patients received first-line b/tsDMARD. First-line treatment was stopped in 3383 (49%) patients; 1263 (37%) were classified as primary failures. The most common reason was "lack of efficacy" (947/2656, 36%). Of the patients who stopped first-line TNFi, 43% (1111/2560) received second-line TNFi, which resulted in the shortest median time to stopping second-line treatment (11 months, 95% CI 9-12) compared with non-TNFi. The longest second-line median treatment duration after first-line TNFi was for patients receiving rituximab (39 months, 95% CI 27-74).
CONCLUSION: A large proportion of patients who stopped first-line TNFi therapy received another TNFi despite evidence for longer treatment persistence on second-line b/tsDMARD with a different mode of action. Lack of efficacy was recorded as the most common reason for making a switch in first-line treatment of patients with RA.

Entities:  

Year:  2019        PMID: 31787605     DOI: 10.3899/jrheum.190535

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  4 in total

1.  Prediction of sustained biologic and targeted synthetic DMARD-free remission in rheumatoid arthritis patients.

Authors:  Theresa Burkard; Ross D Williams; Enriqueta Vallejo-Yagüe; Thomas Hügle; Axel Finckh; Diego Kyburz; Andrea M Burden
Journal:  Rheumatol Adv Pract       Date:  2021-11-13

2.  Interruptions of biological and targeted synthetic disease-modifying antirheumatic drugs in rheumatoid arthritis: a descriptive cohort study assessing trends in patient characteristics in Switzerland.

Authors:  Theresa Burkard; Enriqueta Vallejo-Yagüe; Thomas Hügle; Axel Finckh; Andrea Michelle Burden
Journal:  BMJ Open       Date:  2022-03-15       Impact factor: 2.692

3.  Real-world effectiveness of biological therapy in patients with rheumatoid arthritis: Systematic review and meta-analysis.

Authors:  Caroline Tianeze de Castro; Mariana Jorge de Queiroz; Flavia Caixeta Albuquerque; Celmário Castro Brandão; Leticia Farias Gerlack; Daniella Cristina Rodrigues Pereira; Sandra Castro Barros; Wenderson Walla Andrade; Ediane de Assis Bastos; Jessé de Nobrega Batista Azevedo; Roberto Carreiro; Mauricio Lima Barreto; Djanilson Barbosa Dos Santos
Journal:  Front Pharmacol       Date:  2022-08-11       Impact factor: 5.988

4.  Patterns of biologic and targeted-synthetic disease-modifying antirheumatic drug use in rheumatoid arthritis in Australia.

Authors:  Ashley Fletcher; Marissa Lassere; Lyn March; Catherine Hill; Claire Barrett; Graeme Carroll; Rachelle Buchbinder
Journal:  Rheumatology (Oxford)       Date:  2022-10-06       Impact factor: 7.046

  4 in total

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