OBJECTIVES: To compare the effectiveness and safety of rituximab alone or in combination with either methotrexate or leflunomide. METHODS: 10 European registries submitted anonymised datasets with baseline, 3, 6, 9 and 12-month clinical data from patients who started rituximab. RESULTS: 1195 patients were treated with rituximab plus methotrexate, 177 with rituximab plus leflunomide and 505 with rituximab alone. Significantly more patients achieved a European League Against Rheumatism good response at 6 months when treated with rituximab plus leflunomide (29.1%) compared with rituximab plus methotrexate (21.1%) and rituximab alone (19.3%; p=0.02 and p=0.01, respectively). Similar results were observed at 12 months. Adverse events occurred in...
In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the reference t...
Objective. To assess the safety of treating patients with rheumatoid arthritis with a combination of...
Contains fulltext : 57598.pdf (publisher's version ) (Closed access)In most studie...
To compare the effectiveness and safety of rituximab alone or in combination with either methotrexat...
Objectives To compare the effectiveness and safety of rituximab alone or in combination with either ...
Abstract Background The standard dose of rituximab used in rheumatoid arthritis (RA) is 1000 mg but ...
Introduction: Rituximab (RTX) is a monoclonal anti-CD20 antibody approved for the treatment of rheum...
Objective: In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the ...
Introduction: Rituximab (RTX) is a monoclonal anti-CD20 antibody approved for the treatment of rheum...
Introdiction: Rituximab (RTX) is a monoclonal anti-CD20 antibody approved for the treatment of rheum...
To compare the efficacy and safety of leflunomide (LEF)-anti-TNF-alpha combination therapy to methot...
Background: Several new drugs for rheumatoid arthritis are available including leflunomide. Comparat...
In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the reference t...
Objective To determine the real-life efficacy, safety, and drug-retention rates of leflunomide (LEF)...
International audienceObjective: In rheumatoid arthritis, the association between advanced therapies...
In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the reference t...
Objective. To assess the safety of treating patients with rheumatoid arthritis with a combination of...
Contains fulltext : 57598.pdf (publisher's version ) (Closed access)In most studie...
To compare the effectiveness and safety of rituximab alone or in combination with either methotrexat...
Objectives To compare the effectiveness and safety of rituximab alone or in combination with either ...
Abstract Background The standard dose of rituximab used in rheumatoid arthritis (RA) is 1000 mg but ...
Introduction: Rituximab (RTX) is a monoclonal anti-CD20 antibody approved for the treatment of rheum...
Objective: In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the ...
Introduction: Rituximab (RTX) is a monoclonal anti-CD20 antibody approved for the treatment of rheum...
Introdiction: Rituximab (RTX) is a monoclonal anti-CD20 antibody approved for the treatment of rheum...
To compare the efficacy and safety of leflunomide (LEF)-anti-TNF-alpha combination therapy to methot...
Background: Several new drugs for rheumatoid arthritis are available including leflunomide. Comparat...
In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the reference t...
Objective To determine the real-life efficacy, safety, and drug-retention rates of leflunomide (LEF)...
International audienceObjective: In rheumatoid arthritis, the association between advanced therapies...
In agreement with EULAR recommendations, a DMARD in combination with a biotherapy is the reference t...
Objective. To assess the safety of treating patients with rheumatoid arthritis with a combination of...
Contains fulltext : 57598.pdf (publisher's version ) (Closed access)In most studie...