OUP accepted manuscript
Autor: | Benazir Saleem, Lynda Bailey, Shouvik Dass, Paul Emery, Andrew Melville, L. Garcia-Montoya, Maya H Buch, Yuzaiful Md Yusof, John Fitton |
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Rok vydání: | 2021 |
Předmět: |
030203 arthritis & rheumatology
0301 basic medicine medicine.medical_specialty business.industry Hazard ratio Biosimilar medicine.disease Comorbidity Discontinuation 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Rheumatology Rheumatoid arthritis Internal medicine Medicine Pharmacology (medical) Rituximab In patient business Adverse effect medicine.drug |
Zdroj: | Rheumatology. |
ISSN: | 1462-0332 1462-0324 |
DOI: | 10.1093/rheumatology/keaa834 |
Popis: | Objective To evaluate the impact of non-medical switch from rituximab originator (RTX-O) to biosimilar (RTX-B) in patients with RA. Methods Between October 2017 and October 2019, all patients on RTX-O in our centre requiring re-treatment were switched to RTX-B unless declined by the patient or specified by the treating clinician. Switch strategy effectiveness was assessed retrospectively using DAS28-CRP(3) and RTX retention, with patients remaining on RTX-O as a comparator group. Results The number of patients switching to RTX-B was 255/337 (75.7%) while 82 (24.3%) remained on RTX-O. There was no difference in DAS28-CRP(3) 4 months post-RTX-B switch vs the same time point post-RTX-O previous cycle (paired data available in 60%). Eighteen-month retention estimates were 75.6% (95% CI: 69.4, 80.7%) for RTX-B group and 82.3% (95% CI: 70.4, 89.8%) for RTX-O [adjusted hazard ratio 1.52 (95% CI: 0.85, 2.73)]. The number of patients who discontinued RTX-B for loss of effectiveness (LOE) was 42/255 (16.5%), five (2.0%) for adverse effects (AEs). Risk of RTX-B discontinuation was associated with comorbidities and ≥2 previous biologic DMARDs. Risk of adverse outcome RTX cessation was associated with comorbidities, and reduced risk with number of previous RTX-O cycles and pre-switch cycle B cell depletion. The number of patients who switched back to RTX-O was 34/255 (13.3%) (LOE: 30, AEs: 4), while 13/255 (5.1%) started other biologic/targeted synthetic DMARDs. Of patients who switched back for LOE, 28/30 remained on RTX-O at a mean 7.7 months follow-up. Conclusion Non-medical switch to RTX-B was largely effective. Factors associated with RTX-B discontinuation, including comorbidities, previous biologic DMARDs, and RTX-O treatment history, may inform switch decisions. Most patients who switched back to RTX-O for LOE remained on treatment at short-term follow-up. |
Databáze: | OpenAIRE |
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