Long-term survival of methotrexate in psoriatic arthritis

Objective. The purpose of this study was to evaluate the long-term survival rate of Methotrexate (MTX) in the peripheral joint involvement of psoriatic arthritis (PsA) in a setting of everyday clinical practice. Methods. This was an observational restrospective study performed using the data from a...

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Main Authors: N. Battafarano (Author), L. Rotunno (Author), D. Mazzocchi (Author), F. Desiati (Author), G. De Marco (Author), M. Ricci (Author), A. Marchesoni (Author)
Format: Book
Published: PAGEPress Publications, 2011-06-01T00:00:00Z.
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042 |a dc 
100 1 0 |a N. Battafarano  |e author 
700 1 0 |a L. Rotunno  |e author 
700 1 0 |a D. Mazzocchi  |e author 
700 1 0 |a F. Desiati  |e author 
700 1 0 |a G. De Marco  |e author 
700 1 0 |a M. Ricci  |e author 
700 1 0 |a A. Marchesoni  |e author 
245 0 0 |a Long-term survival of methotrexate in psoriatic arthritis 
260 |b PAGEPress Publications,   |c 2011-06-01T00:00:00Z. 
500 |a 10.4081/reumatismo.2009.125 
500 |a 0048-7449 
500 |a 2240-2683 
520 |a Objective. The purpose of this study was to evaluate the long-term survival rate of Methotrexate (MTX) in the peripheral joint involvement of psoriatic arthritis (PsA) in a setting of everyday clinical practice. Methods. This was an observational restrospective study performed using the data from a dermatological-rheumatological PsA clinic. All of the patients evaluated at this clinic from March 1997 to December 2007 who were started on MTX alone, had a three-year follow-up time or had discontinued the therapy were included into the survey. Results. Of the 174 evaluable patients, 104 (59.8%) were still taking MTX after three years of treament. The reasons of therapy discontinuation in the remaining 70 (40.2%) patients were: 34 (19.5%) lost-to-follow-up, 18 (10.3%) adverse events, 14 (8%) inefficacies, and 4 (2.3%) deaths (none related to the therapy). MTX was effective in controlling joint inflammation but not in preventing their deterioration. Overall, adverse events were recorded in 43 patients (36.4% of the 114 patients with a three-year follow-up). No serious side effect occurred in the study population. Conclusions. The results of this study showed that, in a setting of clinical pratice, MTX had a good three-year performance in patients with peripheral PsA. Almost 60% of them were still taking this drug at the end of the study period and the toxicity was more than acceptable. In our opinion, MTX might be considered the non-biological DMARD of choice for the treatment of this condition. However it should be used earlier and at higher doses. 
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 61, Iss 2, Pp 125-131 (2011) 
787 0 |n http://www.reumatismo.org/index.php/reuma/article/view/426 
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/0c243911f1e64d2f95ff5bd78e0139b0  |z Connect to this object online.