Anti-TNFα therapy in a cohort of rheumatoid arthritis patients: Clinical outcomes

被引:33
作者
Bazzani, Chiara [1 ]
Filippini, Matteo [1 ]
Caporali, Roberto [2 ]
Bobbio-Pallavicini, Francesca [2 ]
Favalli, Ennio Giulio [3 ]
Marchesoni, Antonio [3 ]
Atzeni, Fabiola [4 ]
Sarzi-Puttini, Piercarlo [4 ]
Gorla, Roberto [1 ]
机构
[1] Spedali Civil Brescia, Serv Reumatol & Immunol Clin, Rheumatol & Immunol Unit, I-25123 Brescia, Italy
[2] IRCCS Policlin S Matteo, Chair Rheumatol, Pavia, Italy
[3] Univ Milan, UOC Day Hosp Rheumatol, G Pini Orthoped Inst, Chair Rheumatol, Milan, Italy
[4] L Sacco Univ Hosp, Rheumatol Unit, Milan, Italy
关键词
Disease outcomes; Anti-TNF-alpha treatment; Rheumatoid arthritis; Biological drugs; COLLEGE-OF-RHEUMATOLOGY; DISEASE-ACTIVITY; VALIDATION; REMISSION;
D O I
10.1016/j.autrev.2008.11.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To assess the effectiveness of anti-TNF alpha agents by analysing the principal clinical outcomes in patients with active rheumatoid arthritis (RA). Methods: 1010 patients who received no clinical benefit from previous treatment with methotrexate and/or other DMARDs, were subsequently treated with one or more of the anti-TNF alpha agents. Results: After the first six months of anti-TNF alpha therapy, 29% of the patients showed a good and 47% a moderate European League Against Rheumatism (EULAR) response, and this positive result was maintained after two years of follow-up. Their median Disease Activity Score based on the erythrocyte sedimentation rate and the evaluation of 28 joints (DAS28) decreased from 5.94 at baseline to 4 after six months (p<0.001: Delta 1.94), and further significant responses were also observed after 12, 18 and 24 months; their median 36-month DAS28 score reflected mild disease activity. The median Health Assessment Questionnaire (HAQ) score fell from 1.34 at baseline to 1 after six months of therapy (Delta 0.34; p<0.05), and a further significant reduction was observed during the second and third year of follow up. Conclusions: Especially when combined with DMARDs, anti-TNF alpha drugs can induce a good clinical response regardless of the particular molecule used, whereas their combination with steroids does not seem to improve disease outcomes at any time during follow-up. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:260 / 265
页数:6
相关论文
共 21 条
[1]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[2]   The role of biologic therapies in the management of systemic vasculitis [J].
Chan, A. T. ;
Flossmann, O. ;
Mukhtyar, C. ;
Jayne, D. R. W. ;
Luqmani, R. A. .
AUTOIMMUNITY REVIEWS, 2006, 5 (04) :273-278
[3]   DAS28 best reflects the physician's clinical judgment of response to infliximab therapy in rheumatoid arthritis patients: validation of the DAS28 score in patients under infliximab treatment [J].
Cruyssen, BV ;
Van Looy, S ;
Wyns, B ;
Westhovens, R ;
Durez, P ;
Malaise, M ;
Verbruggen, L ;
Vastesaeger, N ;
Geldhof, A ;
Boullart, L ;
De Keyser, F .
ARTHRITIS RESEARCH & THERAPY, 2005, 7 (05) :R1063-R1071
[4]   AMERICAN-COLLEGE-OF-RHEUMATOLOGY PRELIMINARY DEFINITION OF IMPROVEMENT IN RHEUMATOID-ARTHRITIS [J].
FELSON, DT ;
ANDERSON, JJ ;
BOERS, M ;
BOMBARDIER, C ;
FURST, D ;
GOLDSMITH, C ;
KATZ, LM ;
LIGHTFOOT, R ;
PAULUS, H ;
STRAND, V ;
TUGWELL, P ;
WEINBLATT, M ;
WILLIAMS, HJ ;
WOLFE, F ;
KIESZAK, S .
ARTHRITIS AND RHEUMATISM, 1995, 38 (06) :727-735
[5]  
Fransen J, 2005, CLIN EXP RHEUMATOL, V23, pS93
[6]   Predictors of response to anti-TNF-α therapy among patients with rheumatoid arthritis:: results from the British Society for Rheumatology Biologics Register [J].
Hyrich, K. L. ;
Watson, K. D. ;
Silman, A. J. ;
Symmons, D. P. M. .
RHEUMATOLOGY, 2006, 45 (12) :1558-1565
[7]  
Kosinski M, 2000, ARTHRITIS RHEUM-US, V43, P1478, DOI 10.1002/1529-0131(200007)43:7<1478::AID-ANR10>3.0.CO
[8]  
2-M
[9]  
Mullan RH, 2003, CLIN EXP RHEUMATOL, V21, pS158
[10]  
Pincus T, 2006, CLIN EXP RHEUMATOL, V24, pS1