Adverse events and efficacy of TNF-α blockade with infliximab in patients with systemic lupus erythematosus: long-term follow-up of 13 patients

被引:130
作者
Aringer, Martin [1 ,2 ]
Houssiau, Frederic [3 ]
Gordon, Caroline [4 ]
Graninger, Winfried B. [5 ]
Voll, Reinhard E. [6 ,7 ]
Rath, Eva [2 ]
Steiner, Guenter [2 ]
Smole, Josef S. [2 ]
机构
[1] Tech Univ Dresden, Dept Med 3, Div Rheumatol, Univ Clin Ctr Carl Gustav Carus, D-01307 Dresden, Germany
[2] Med Univ Vienna, Dept Rheumatol, Vienna, Austria
[3] Univ Catholique Louvain, Dept Rheumatol, Clin Univ St Luc, B-1200 Brussels, Belgium
[4] Univ Birmingham, Sch Immun & Infect, Coll Med & Dent Sci, Birmingham, W Midlands, England
[5] Med Univ Graz, Dept Med, Div Rheumatol, Graz, Austria
[6] Univ Erlangen Nurnberg, Dept Internal Med 3, Univ Hosp Erlangen, Erlangen, Germany
[7] Univ Erlangen Nurnberg, Inst Clin Immunol, Univ Hosp Erlangen, Erlangen, Germany
关键词
Systemic lupus erythematosus; Lupus nephritis; Tumor necrosis factor-alpha; Infliximab; Safety; TUMOR-NECROSIS-FACTOR; MONOCLONAL-ANTIBODY; OPEN-LABEL; MICE; ARTHRITIS; THERAPY; INHIBITION; NEPHRITIS; LYMPHOMA;
D O I
10.1093/rheumatology/kep270
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To follow-up on all available infliximab-treated SLE patients for safety and long-term efficacy in order to extract information that is useful for planning appropriate controlled trials with infliximab in SLE. Methods. We analysed charts of six patients treated in an open-label safety trial and seven additional patients treated with infliximab on a compassionate care basis for uncontrolled SLE organ inflammation. Results. Out of nine patients with lupus nephritis, six had a long-term response after four infusions of infliximab in combination with AZA, lasting for up to 5 years. All five patients with lupus arthritis responded, but this response did not last for >2 months after the last infusion. One additional patient had a long-lasting improvement in SLE interstitial lung disease. No symptoms suggestive of infliximab-induced SLE flares occurred in any patients. Short-term treatment appeared relatively safe, but one patient developed deep-vein thrombosis and several infections. Under long-term therapy, two patients had life-threatening or fatal events, namely CNS lymphoma and Legionella pneumonia. Retreatment and treatment without concomitant immunosuppression led to drug reactions. Conclusions. Short-term therapy with four infusions of infliximab in combination with AZA was relatively safe, and had remarkable long-term efficacy for lupus nephritis and, potentially, also interstitial lung disease. Long-term therapy with infliximab, however, was associated with severe adverse events in two out of three SLE patients, which may have been provoked by infliximab and/or by their long-standing refractory SLE and previous therapies.
引用
收藏
页码:1451 / 1454
页数:4
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