The addition of tocilizumab to DMARD therapy for rheumatoid arthritis: a meta-analysis of randomized controlled trials.

Tocilizumab is a humanized monoclonal antibody that binds to the interleukin-6 receptor. The purpose of this study was to evaluate the effect of adding tocilizumab to disease-modifying antirheumatic drug (DMARD) therapy for the treatment of rheumatoid arthritis (RA). We performed a meta-analysis of...

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Publicado en:European Journal of Clinical Pharmacology Vol. 66; no. 1; pp. 49 - 60
Autores principales: An M, Zou Z, Shen H, Zhang J, Cao Y, Jiang Y
Formato: research systematic review Journal Article
Publicado: Springer Nature Jan2010
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2010
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      pub: Springer Nature
      place: New York, New York
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        atl: The addition of tocilizumab to DMARD therapy for rheumatoid arthritis: a meta-analysis of randomized controlled trials.
      aug:
        au:
          An M
          Zou Z
          Shen H
          Zhang J
          Cao Y
          Jiang Y
        affil: Department of Anesthesiology, Changzheng Hospital, Second Military Medical University, Shanghai 200433 People's Republic of China
      sug:
        subj:
          Antibodies, Monoclonal Therapeutic Use
          Antirheumatic Agents Therapeutic Use
          Combined Modality Therapy Evaluation
          Tocilizumab
          Arthritis, Rheumatoid Complications
          Chronic Disease Diagnosis
          Cochrane Library
          Confidence Intervals
          Data Analysis Methods
          Data Collection
          Databases
          Embase
          Immunity
          Inflammation Physiopathology
          Interleukins
          Joints Physiopathology
          Medical Organizations
          Meta Analysis
          Outcomes (Health Care)
          Pharmacy and Pharmacology
          PubMed
      ab: Tocilizumab is a humanized monoclonal antibody that binds to the interleukin-6 receptor. The purpose of this study was to evaluate the effect of adding tocilizumab to disease-modifying antirheumatic drug (DMARD) therapy for the treatment of rheumatoid arthritis (RA). We performed a meta-analysis of relevant randomized controlled trials (RCTs) identified in PubMed, Cochrane library, and Embase. The primary efficacy outcome was the proportion of patients with a 20% improvement in RA signs and symptoms according to American College of Rheumatology (ACR) criteria (ACR20 response). The primary safety outcomes were the proportion of patients reporting at least one adverse event and the proportion of patients reporting at least one serious adverse event. Four RCTs, involving 2701 patients, were included in our meta-analysis. The addition of tocilizumab to therapeutic regimens with DMARDs was associated both clinically and statistically with an increased number of patients achieving the ACR20 response [8 mg/kg, risk ratio (RR) 2.53, 95% confidence interval (CI) 1.89-3.39; 4 mg/kg, RR 1.96, 95% CI 1.40-2.73], as well as the ACR50 and ACR70 response, and showing remission according to the Disease Activity Score based on 28 joints. However, the benefits were gained at the expense of the tendency of the patient to experience more adverse events (8 mg/kg, RR 1.12, 95% CI 1.03-1.20; 4 mg/kg, RR 1.08, 95% CI 1.00-1.17). The new finding was that the clinical benefit from the increased tocilizumab dose (from 4 to 8 mg/kg) was not correlated with a higher incidence of adverse events. The superior efficacy of combined tocilizumab + DMARD therapy is associated with the tendency for the patient to have more adverse events. Consequently, the benefits and disadvantages of such combined treatments should be carefully balanced against each other in RA therapy. We suggest that 8 mg/kg every 4 weeks should be the recommended dose of tocilizumab.
      pubtype: Academic Journal
      doctype:
        research
        systematic review
        Journal Article
      ougenre: Article
    language: English
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