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Use of tofacitinib in real clinical practice to treat patients with rheumatoid arthritis resistant to synthetic and biological disease-modifying antirheumatic drugs: Results of a multicenter observational study

https://doi.org/10.14412/1996-7012-2016-3-52-61

Abstract

Tofacitinib (TOFA), a member of a new class of targeted synthetic disease-modifying antirheumatic drugs (DMARDs), is a promising medication for the treatment of rheumatoid arthritis (RA) and other immunoinflammatory diseases. The paper describes the Russian experi-ence with TOFA used to treat severe RA.

Patients and methods. 101 RA patients (18 men and 83 women; mean age, 51.03±11.28 years; mean disease duration, 105.4±81.43 months) who were positive for rheumatoid factor (89.1%) and anti-cyclic citrullinated peptide antibodies (74.7%) and resistant to therapy with synthetic DMARDs (sDMARDs) (80.2%) and biological agents (19.8%) were given TOFA at a dose of 5 mg twice daily, which could be doubled if necessary. TOFA was used alone (n=9) or in combination with methotrexate (MT) (n=75) or other sDMARDs (n=17). The achievement of low disease activity (LDA) and clinical remission at 3 and 6 months of treatment by DAS28-ESR SDAI, and CDAI scores, and the indices of safety and tolerability were assessed.

Results. A total of 93 (92.1%) of the 101 patients completed a 24-week period of the investigation. 8 (7.9%) patients prematurely discontinued TOFA after an average of 2.75±0.71 months. At the end of the study, the patients achieved the primary endpoint (LDA including remission) in terms of DAS28-ESR ≤3.2 (34.7%), SDAI ≤11 (47.5%), and CDAI ≤10 (48.5%) and the secondary endpoints (clinical remission) in terms of DAS28-ESR ≤2.6 (17.8%), SDAI ≤3.3 (8.9%), and CDAI ≤2.8 (6.9%). When TOFA was combined with MT, the discontinuation rate for the former was significantly lower (2.7%) than when TOFA was used in combination with other sDMARDs (29.4%) or alone (11.1%; p<0.01). At 3 and 6 months of follow-up, LDA was achieved more frequently when TOFA was combined with MT than when other treatment regimens were used. Fatal outcomes and serious adverse events (AEs), as AEs previously undescribed in the literature, were not seen during a follow-up within the framework of the clinical trial. Only 2 patients discontinued TOFA because of AEs.

Conclusion. The use of TOFA in RA is effective in achieving LDA in patients unresponsive to sDMARDs and biological DMARDs. The prescription of the drug makes it possible to monitor the activity of the inflammatory process and, with its sufficient safety and good tolerability, to achieve LDA in half of the patients, including those with multidrug resistance.

About the Authors

D. E. Karateev
V.A. Nasonova Research Institute of Rheumatology, Moscow, Russia 34A, Kashirskoe Shosse, Moscow 115522
Russian Federation


D. E. Abdulganieva
Republican Clinical Hospital, Ministry of Health of the Republic of Tatarstan, Kazan, Russia 138, Orenburgsky Road, Kazan, Republic of Tatarstan 420064
Russian Federation


A. R. Babaeva
City Clinical Hospital Four, Volgograd, Russia 40, Opolchenskaya St., Volgograd 400065
Russian Federation


A. A. Baranov
Yaroslavl State Medical University, Ministry of Health of Russia, Yaroslavl, Russia 5, Revolyutsionnaya St., Yaroslavl 150000
Russian Federation


L. P. Evstigneeva
Sverdlovsk Regional Clinical Hospital One, Yekaterinburg, Russia 185, Volgogradskaya St., Yekaterinburg 620102
Russian Federation


O. N. Ivanova
Voronezh Regional Clinical Hospital One, Voronezh, Russia 151, Moskovsky Prospect, Voronezh 394066
Russian Federation


G. V. Lukina
V.A. Nasonova Research Institute of Rheumatology, Moscow, Russia 34A, Kashirskoe Shosse, Moscow 115522 Moscow Clinical Research and Practical Center, Moscow Healthcare Department, Moscow, Russia 86, Shosse Entuziastov, Moscow 111123
Russian Federation


E. L. Luchikhina
V.A. Nasonova Research Institute of Rheumatology, Moscow, Russia 34A, Kashirskoe Shosse, Moscow 115522
Russian Federation


V. I. Mazurov
I.I. Mechnikov North-Western State Medical University, Ministry of Health of Russia, Saint Petersburg, Russia 41, Kirochnaya St., Saint Petersburg 191015
Russian Federation


A. S. Misiyuk
V.A. Nasonova Research Institute of Rheumatology, Moscow, Russia 34A, Kashirskoe Shosse, Moscow 115522
Russian Federation


O. V. Semagina
M.I. Kalinin Samara Regional Hospital, Samara, Russia 159, Tashkentskaya St., Samara 443095
Russian Federation


A. E. Sizikov
Research Institute of Fundamental and Clinical Immunology, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia 2/1, Zalessky St., Novosibirsk 630047
Russian Federation


V. N. Sorotskaya
Tula Regional Clinical Hospital, Tula, Russia 1a, Yablochkov St., Tula 300053
Russian Federation


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Karateev DE, Abdulganieva DE, Babaeva AR, Baranov AA, Evstigneeva LP, Ivanova ON, Lukina GV, Luchikhina EL, Mazurov VI, Misiyuk AS, Semagina OV, Sizikov AE, Sorotskaya VN. Use of tofacitinib in real clinical practice to treat patients with rheumatoid arthritis resistant to synthetic and biological disease-modifying antirheumatic drugs: Results of a multicenter observational study. Sovremennaya Revmatologiya=Modern Rheumatology Journal. 2016;10(3):52-61. (In Russ.) https://doi.org/10.14412/1996-7012-2016-3-52-61

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ISSN 1996-7012 (Print)
ISSN 2310-158X (Online)