Effect of baseline rheumatoid factor and anticitrullinated peptide antibody serotype on rituximab clinical response: a meta-analysis

被引:153
作者
Isaacs, John D. [1 ,2 ]
Cohen, Stanley B. [3 ]
Emery, Paul [4 ]
Tak, Paul P. [5 ,6 ]
Wang, Jianmei [7 ]
Lei, Guiyuan [7 ]
Williams, Sarah [7 ]
Lal, Preeti [8 ]
Read, Simon J. [7 ]
机构
[1] Newcastle Univ, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
[2] Newcastle Upon Tyne Hosp NHS Fdn Trust, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England
[3] Metroplex Clin Res Ctr, Dallas, TX USA
[4] Leeds Gen Infirm, Leeds, W Yorkshire, England
[5] AMC Univ Amsterdam, Dept Clin Immunol & Rheumatol, Amsterdam, Netherlands
[6] GlaxoSmithKline, Stockley Pk, Middx, England
[7] Roche Prod Ltd, Welwyn Garden City AL7 3AY, Herts, England
[8] Genentech Inc, San Francisco, CA 94080 USA
关键词
AUTOANTIBODY STATUS RF; TUMOR-NECROSIS-FACTOR; 1ST-TREATMENT COURSE; DOUBLE-BLIND; ARTHRITIS; THERAPY; SAFETY; PREDICTORS; EFFICACY; METHOTREXATE;
D O I
10.1136/annrheumdis-2011-201117
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Studies examining the relationship between serological status (rheumatoid factor and/or anticitrullinated antibody) and rituximab treatment outcome in rheumatoid arthritis (RA) have been hampered by limited numbers of seronegative patients. Objective To carry out a meta-analysis of trials from the rituximab RA clinical programme to investigate this relationship further. Methods This was a meta-analysis of four placebo-controlled, phase II or III clinical trials. The efficacy end point in all analyses was change from baseline in Disease Activity Score in 28 joints-erythrocyte sedimentation rate (DAS28-ESR) at 24 weeks. Assay of serotype and missing data imputation methods were consistent across all studies. Results The population analysed comprised 2177 patients (rituximab, n=1416; placebo, n=761). Demographics and baseline disease characteristics were well balanced. When a fixed-effects meta-analysis approach was used, the overall-effect model indicated evidence of additional treatment benefit with rituximab in seropositive patients: reduction in DAS28-ESR at week 24 was on average 0.35 units (95% CI 0.12 to 0.84; n=1394) greater than in seronegative patients; this effect was not seen in placebo patients. Heterogeneity indices indicated significant uncertainty in the overall-effect model (Q=8.8, I=0.77; p=0.03 (chi(2) test)). Baseline Health Assessment Questionnaire score, pain visual analogue scale, swollen joint counts of 28 joints and race were significant contributors to this heterogeneity, with additional analysis indicating that these effects may predominate in early RA (methotrexate-naive) populations. A dominant effect was seen in patients for whom one or more tumour necrosis factor inhibitors had failed. Conclusion Although the difference was modest, the overall-effect model indicates that seropositive patients respond better to rituximab than seronegative patients.
引用
收藏
页码:329 / 336
页数:8
相关论文
共 30 条
[1]
[Anonymous], ANN RHEUM DIS
[2]
[Anonymous], RHEUMATOLOGY OXFORD
[3]
High IgA rheumatoid factor levels are associated with poor clinical response to tumour necrosis factor a inhibitors in rheumatoid arthritis [J].
Bobbio-Pallavicini, Francesca ;
Caporali, Roberto ;
Alpini, Claudia ;
Avalle, Stefano ;
Epis, Oscar M. ;
Klersy, Catherine ;
Montecucco, Carlomaurizio .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (03) :302-307
[4]
Updated consensus statement on the use of rituximab in patients with rheumatoid arthritis [J].
Buch, Maya H. ;
Smolen, Josef S. ;
Betteridge, Neil ;
Breedveld, Ferdinand C. ;
Burmester, Gerd ;
Doerner, Thomas ;
Ferraccioli, Gianfranco ;
Gottenberg, Jacques-Eric ;
Isaacs, John ;
Kvien, Tore K. ;
Mariette, Xavier ;
Martin-Mola, Emilio ;
Pavelka, Karel ;
Tak, Paul P. ;
van der Heijde, Desiree ;
van Vollenhoven, Ronald F. ;
Emery, Paul .
ANNALS OF THE RHEUMATIC DISEASES, 2011, 70 (06) :909-920
[5]
Effectiveness and safety of the interleukin 6-receptor antagonist tocilizumab after 4 and 24 weeks in patients with active rheumatoid arthritis: the first phase IIIb real-life study (TAMARA) [J].
Burmester, Gerd R. ;
Feist, E. ;
Kellner, H. ;
Braun, J. ;
Iking-Konert, C. ;
Rubbert-Roth, A. .
ANNALS OF THE RHEUMATIC DISEASES, 2011, 70 (05) :755-759
[6]
Highest clinical effectiveness of rituximab in autoantibody-positive patients with rheumatoid arthritis and in those for whom no more than one previous TNF antagonist has failed: pooled data from 10 European registries [J].
Chatzidionysiou, Katerina ;
Lie, Elisabeth ;
Nasonov, Evgeny ;
Lukina, Galina ;
Hetland, Merete Lund ;
Tarp, Ulrik ;
Gabay, Cem ;
van Riel, Piet L. C. M. ;
Nordstrom, Dan C. ;
Gomez-Reino, Juan ;
Pavelka, Karel ;
Tomsic, Matija ;
Kvien, Tore K. ;
van Vollenhoven, Ronald F. .
ANNALS OF THE RHEUMATIC DISEASES, 2011, 70 (09) :1575-1580
[7]
Rituximab for rheumatoid arthritis refractory to anti-tumor necrosis factor therapy - Results of a multicenter, randomized, double-blind, placebo-controlled, phase III trial evaluating primary efficacy and safety at twenty-four weeks [J].
Cohen, Stanley B. ;
Emery, Paul ;
Greenwald, Maria W. ;
Dougados, Maxime ;
Furie, Richard A. ;
Genovese, Mark C. ;
Keystone, Edward C. ;
Loveless, James E. ;
Burmester, Gerd-Ruediger ;
Cravets, Matthew W. ;
Hessey, Eva W. ;
Shaw, Timothy ;
Totoritis, Mark C. .
ARTHRITIS AND RHEUMATISM, 2006, 54 (09) :2793-2806
[8]
Cuchacovich M, 2008, CLIN EXP RHEUMATOL, V26, P1067
[9]
Drynda S, 2008, ARTHRITIS RHEUM, V58, pS211
[10]
The efficacy and safety of rituximab in patients with active rheumatoid arthritis despite methotrexate treatment - Results of a phase IIb randomized, double-blind, placebo-controlled, dose-ranging trial [J].
Emery, P ;
Fleischmann, R ;
Filipowicz-Sosnowska, A ;
Schechtman, J ;
Szczepanski, L ;
Kavanaugh, A ;
Racewicz, AJ ;
Van Vollenhoven, RF ;
Li, NF ;
Agarwal, S ;
Hessey, EW ;
Shaw, TM .
ARTHRITIS AND RHEUMATISM, 2006, 54 (05) :1390-1400