Treatment of rheumatoid arthritis with anti-TNF-alpha agents: A reappraisal

被引:100
作者
Caporali, Roberto [1 ]
Pallavicini, Francesca Bobbio [1 ]
Filippini, Matteo [2 ]
Gorla, Roberto [2 ]
Marchesoni, Antonio [3 ]
Favalli, Ennio Giulio [3 ]
Sarzi-Puttini, Piercarlo [4 ]
Atzeni, Fabiola [4 ]
Montecucco, Carlornaurizio [1 ]
机构
[1] Univ Pavia, Rheumatol Unit, IRCCS Policlin S Matteo Fdn, I-27100 Pavia, Italy
[2] Spedali Civil Brescia, Rheumatol & Immunol Unit, I-25125 Brescia, Italy
[3] Day Hosp Rheumatol, G Pini Orthopaed Inst, Milan, Italy
[4] L Sacco Univ Hosp, Rheumatol Unit, Milan, Italy
关键词
Anti-tumour necrosis factor (TNF); Rheumatoid arthritis (RA); Disease modifying anti-rheumatic drugs; (DMARDs); Methotrexate (MTX); RANDOMIZED CONTROLLED-TRIALS; NECROSIS-FACTOR BLOCKERS; DOUBLE-BLIND; METHOTREXATE THERAPY; MONOCLONAL-ANTIBODY; CLINICAL-PRACTICE; INFLIXIMAB; ETANERCEPT; RISK; EPIDEMIOLOGY;
D O I
10.1016/j.autrev.2008.11.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has been found that tumour necrosis factor(TNF)-alpha plays a pivotal role in the pathogenesis of rheumatoid arthritis (RA), and the development of drugs targeting this molecule has extended the therapeutical approaches to RA patients. A number of observational studies of large patient series have also been published over the last few years, many of which have been based on national registries designed to monitor the efficacy and safety of anti-TNF agents, and allow healthcare institutions to control expenditure. Registry data can also help in identifying clinical and laboratory findings capable of predicting response. It has been suggested that the percentage of responding patients is lower in everyday clinical practice than that observed in RCTs, possibly because of patient selection, the use of a washout period before inclusion (which may artificially increase disease activity). and differences in doses, co-morbidities and adherence to therapy. A number of safety concerns have been raised since the introduction of anti-TNF agents, and they are now contraindicated in patients with advanced heart failure; however, the most widely debated current issues regard infections and neoplastic diseases. Moreover, the marketing of new and expensive biological agents has made strictly necessary to create systems capable of monitoring their safety and effectiveness in everyday practice, including the use of longitudinal observational studies. As the first published registry of anti-TNF alpha-treated patients in Italy. Lombardy Rheumatology Network (LORHEN) is already making its contribution in this direction. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:274 / 280
页数:7
相关论文
共 41 条
[1]  
Allaart CF, 2007, J RHEUMATOL, V34, P25
[2]   The safety of anti-tumour necrosis factor therapy in rheumatoid arthritis [J].
Askling, Johan ;
Dixon, Will .
CURRENT OPINION IN RHEUMATOLOGY, 2008, 20 (02) :138-144
[3]   Potential target of infliximab in autoimmune and inflammatory diseases [J].
Atzeni, Fabiola ;
Doria, Andrea ;
Carrabba, Mario ;
Turiel, Maurizio ;
Sarzi-Puttini, Piercarlo .
AUTOIMMUNITY REVIEWS, 2007, 6 (08) :529-536
[4]   Anti-TNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies - Systematic review and meta-analysis of rare harmful effects in randomized controlled trials [J].
Bongartz, T ;
Sutton, AJ ;
Sweeting, MJ ;
Buchan, I ;
Matteson, EL ;
Montori, V .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (19) :2275-2285
[5]   The PREMIER study - A multicenter, randomized, double-blind clinical trial of combination therapy with adalimumab plus methotrexate versus methotrexate alone or adalimumab alone in patients with early, aggressive rheumatoid arthritis who had not had previous methotrexate treatment [J].
Breedveld, FC ;
Weisman, MH ;
Kavanaugh, AF ;
Cohen, SB ;
Pavelka, K ;
van Vollenhoven, R ;
Sharp, J ;
Perez, JL ;
Spencer-Green, GT .
ARTHRITIS AND RHEUMATISM, 2006, 54 (01) :26-37
[6]   All-cause and cause-specific mortality in rheumatoid arthritis are not greater than expected when treated with tumour necrosis factor antagonists [J].
Carmona, Loreto ;
Descalzo, Miguel Angel ;
Perez-Pampin, Eva ;
Ruiz-Montesinos, Dolores ;
Erra, Alba ;
Cobo, Tatiana ;
Gomez-Reino, Juan J. .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (07) :880-885
[7]   Mechanisms of disease: Cytokine pathways and joint inflammation in rheumatoid arthritis. [J].
Choy, EHS ;
Panayi, GS .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (12) :907-916
[8]   Combination of infliximab and methotrexate therapy for early rheumatoid arthritis - A randomized, controlled trial [J].
Clair, EWS ;
van der Heijde, DMFM ;
Smolen, JS ;
Maini, RN ;
Bathon, JM ;
Emery, P ;
Keystone, E ;
Schiff, M ;
Kalden, JR ;
Wang, B ;
DeWoody, K ;
Weiss, R ;
Baker, D .
ARTHRITIS AND RHEUMATISM, 2004, 50 (11) :3432-3443
[9]   Problems encountered during anti-tumour necrosis factor therapy [J].
Desai, Sheetal B. ;
Furst, Daniel E. .
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2006, 20 (04) :757-790
[10]   Tumour necrosis factor blockers do not increase overall tumour risk in patients with rheumatoid arthritis, but may be associated with an increased risk of lymphomas [J].
Geborek, P ;
Bladström, A ;
Turesson, C ;
Gulfe, A ;
Petersson, IF ;
Saxne, T ;
Olsson, H ;
Jacobsson, LTH .
ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (05) :699-703