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Safety and effectiveness of rituximab in patients with rheumatoid arthritis following an inadequate response to 1 prior tumor necrosis factor inhibitor: the RESET Trial
- Source :
- The Journal of rheumatology. 38(12)
- Publication Year :
- 2011
-
Abstract
- Objective.To evaluate the safety and effectiveness of rituximab (RTX) in combination with methotrexate in patients with active rheumatoid arthritis (RA) after failure of a single tumor necrosis factor-α (TNF-α) inhibitor. Changes in patient-reported outcomes after primary treatment or retreatment with RTX and factors determining retreatment in clinical practice were also evaluated.Methods.In this phase 3b open-label, multicenter trial, patients received 2 slow infusions of RTX 1000 mg 14 days apart after premedication (primary treatment). Patients with a clinically relevant response could receive retreatment between 24 and 48 weeks. The primary endpoint was evaluation of safety. Secondary outcomes were safety of retreatment, effectiveness of primary treatment and retreatment, and changes in patient-reported outcomes after primary treatment or retreatment.Results.Of 120 patients enrolled at 36 centers and receiving primary RTX treatment, 77 received retreatment, 112 completed the 24-week primary treatment period, and 25 completed the 48-week primary treatment and retreatment period following a single course of RTX. The most common adverse events were mild to moderate nausea, vomiting, nasopharyngitis, and headache. No infections or infusion reactions were considered life-threatening. At 24 weeks, 58%, 27%, and 7% of patients achieved American College of Rheumatology 20, 50, and 70 improvements, respectively, and similar improvements were seen after retreatment.Conclusion.RTX was well tolerated, with a low incidence of infusion reactions and infections. Efficacy results, including enhanced response in rheumatoid factor-positive patients, were comparable to those reported in the literature. Based on its efficacy and safety profile and retreatment schedule, RTX is an attractive treatment option for patients that have not responded to a single TNF-α inhibitor.
- Subjects :
- Adult
Male
medicine.medical_specialty
Nausea
Immunology
Arthritis, Rheumatoid
Antibodies, Monoclonal, Murine-Derived
Rheumatology
Multicenter trial
Internal medicine
medicine
Clinical endpoint
Immunology and Allergy
Humans
Prospective Studies
Adverse effect
Aged
business.industry
Tumor Necrosis Factor-alpha
Middle Aged
medicine.disease
Surgery
Methotrexate
Treatment Outcome
Rheumatoid arthritis
Antirheumatic Agents
Rituximab
Premedication
Drug Therapy, Combination
Female
medicine.symptom
business
medicine.drug
Subjects
Details
- ISSN :
- 0315162X
- Volume :
- 38
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- The Journal of rheumatology
- Accession number :
- edsair.doi.dedup.....33721337f9f9be222a76c5c3a6a4dd85