Anakinra, a recombinant human IL-1 receptor antagonist, in clinical practice. Outcome in 60 patients with severe rheumatoid arthritis

Objective: We evaluated both the efficacy and safety of anakinra in daily routine rheumatoid arthritis clinical practice. Methods:We studied 60 cases, including patients with previous anti-TNFα exposure, treated with anakinra (100 mg/daily s.c.) in combination with methotrexate (7.5-10 mg/week i.m.)...

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Main Authors: S. Todesco (Author), U. Fiocco (Author), M. Biscaro (Author), P. Ostuni (Author), A. Furlan (Author), P. Sfriso (Author), C. Botsios (Author), L. Punzi (Author)
Format: Book
Published: PAGEPress Publications, 2011-09-01T00:00:00Z.
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042 |a dc 
100 1 0 |a S. Todesco  |e author 
700 1 0 |a U. Fiocco  |e author 
700 1 0 |a M. Biscaro  |e author 
700 1 0 |a P. Ostuni  |e author 
700 1 0 |a A. Furlan  |e author 
700 1 0 |a P. Sfriso  |e author 
700 1 0 |a C. Botsios  |e author 
700 1 0 |a L. Punzi  |e author 
245 0 0 |a Anakinra, a recombinant human IL-1 receptor antagonist, in clinical practice. Outcome in 60 patients with severe rheumatoid arthritis 
260 |b PAGEPress Publications,   |c 2011-09-01T00:00:00Z. 
500 |a 10.4081/reumatismo.2007.32 
500 |a 0048-7449 
500 |a 2240-2683 
520 |a Objective: We evaluated both the efficacy and safety of anakinra in daily routine rheumatoid arthritis clinical practice. Methods:We studied 60 cases, including patients with previous anti-TNFα exposure, treated with anakinra (100 mg/daily s.c.) in combination with methotrexate (7.5-10 mg/week i.m.) or leflunomide (20 mg/die) in a two year observational study. Efficacy measures were assessed using the American College of Rheumatology (ACR) response criteria. Safety was evaluated according to a modified World Health Organization adverse reaction term dictionary. Results: At week 14, ACR 20% response criteria have been fulfilled by 53 (91.3%) out of 58 patients, 51 (87.9%) of them achieving also an ACR 50%and 15 (25.8%) an ACR 70%response. Thirteen patients touched 102 weeks of treatment: ACR 20% response was achieved in 92.3%, while ACR 50% and ACR 70% were respectively found in 84.6% and 38.4% of the cases. The mean decrease in HAQ score was 0.38, p<0.001. Of the 16 patients who were previously treated with anti-TNFα blockers, 81.2% responded to anakinra. There was no significant difference in the ACR response between groups with and without previous anti-TNFα exposure. Seventeen patients (28.3%) stopped anakinra because of side-effects (5%) or failure to respond (23.3%). Only 4 cases of pulmonitis, of which 2 have been hospitalised, and 1 case with tuberculosis (previously treated with infliximab) were observed. Conclusions: Our clinical experience confirms that anakinra is effective and safe in the treatment of rheumatoid arthritis. Anakinra seems also useful in patients with previous anti-TNFα blockers failures. Even though major adverse events were rare, clinicians should be aware of such a possibility 
546 |a EN 
546 |a IT 
690 |a Medicine 
690 |a R 
690 |a Internal medicine 
690 |a RC31-1245 
655 7 |a article  |2 local 
786 0 |n Reumatismo, Vol 59, Iss 1, Pp 32-37 (2011) 
787 0 |n http://www.reumatismo.org/index.php/reuma/article/view/293 
787 0 |n https://doaj.org/toc/0048-7449 
787 0 |n https://doaj.org/toc/2240-2683 
856 4 1 |u https://doaj.org/article/5d0e3d11f15e4cd88cdf87bb19fe026f  |z Connect to this object online.