The efficiency and safety of adalimumab treatment in patients with active rheumatoid arthritis unresponsive to standard therapy: Russian national study results
| Autor: | Karateev, D. E., Nasonov, E. L., Luchikhina, E. L., Vadim Mazurov, Salikhov, I. G., Shmidt, E. I., Shostak, N. A. |
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| Jazyk: | ruština |
| Rok vydání: | 2012 |
| Předmět: | |
| Zdroj: | Терапевтический архив, Vol 84, Iss 8, Pp 22-28 (2012) Scopus-Elsevier |
| ISSN: | 2309-5342 0040-3660 |
| Popis: | Aim. To confirm the efficacy and safety of adalimumab (ADA) added to the standard antirheumatic therapy performed in patients with rheumatoid arthritis (RA) of moderate and high activities.Subjects and methods. The open-labeled multicenter study enrolled 100 adult patients (11 men, 89 women; mean age 50.9±11.1 years) with active RA according to the ACR criteria (1987) despite their treatment with disease-modifying antirheumatic drugs, the average number of which in the history was 2.1 per man. At baseline, DAS28 CRP was as many as 6.2±0.84 scores; C-reactive protein (CRP) was 37.1±34.7 mg/l. In accordance with the indications officially registered in the European Union and the Russian Federation, ADA was given in a dose of 40 mg 2 weeks. Before administration of the drug, every patient underwent screening examination for tuberculosis, which used a tuberculin test and chest X-ray. The screening covered a period of the treatment up to 24 weeks and its subsequent period within 70 days after administration of the last dose of ADA in order to study its safety. Results. DAS28-CRP scores decreased from 6.14±0.86 (at baseline) to 3.39±1.1 (by the end of the study). At 12 weeks, 22% of the patients achieved a low RA activity (DAS28-CRP ≤3.2 scores); 14% achieved clinical remission ((DAS28-CRP ≤2.6 scores); at 24 weeks, these were 37 and 25% of the patients, respectively. There were differences in effectiveness in terms of the baseline disease activity. At 24 weeks, ACR20, ACR50, and ACR 70 responses were achieved in 88, 67, and 26% of the patients, respectively. The HAQ functional index reduced from 1.9±0.6 (at baseline) to 1.081±0.64 (at 12 weeks) and 1.04±0.68 (at 24 weeks) scores. Twenty-four patients were recorded as having 40 adverse reactions (AR), including only one severe AR (septic arthritis). There were no cases of tuberculosis. Conclusion. The Russian multicenter study demonstrated the high clinical efficacy of ADA in patients with the moderate and high activity of RA unresponsive to standard therapy, as well as its satisfactory safety. |
| Databáze: | OpenAIRE |
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