Influence of anti-infliximab antibodies and residual infliximab concentrations on the occurrence of acquired drug resistance to infliximab in rheumatoid arthritis patients

被引:35
作者
Finckh, Axel [1 ]
Dudler, Jean [2 ]
Wermelinger, Felix [3 ]
Ciurea, Adrian [4 ]
Kyburz, Diego [4 ]
Gabay, Cem [1 ]
Bas, Sylvette [1 ,5 ]
机构
[1] Univ Hosp Geneva, Div Rheumatol, Dept Internal Med, CH-1211 Geneva, Switzerland
[2] Vaud Univ Hosp Ctr, Div Rheumatol, Lausanne, Switzerland
[3] Univ Hosp Bern, Dept Rheumatol Clin Immunol & Allergy, CH-3010 Bern, Switzerland
[4] Univ Zurich Hosp, Dept Rheumatol, CH-8091 Zurich, Switzerland
[5] Univ Hosp Geneva, Dept Genet & Lab Med, CH-1211 Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
Rheumatoid arthritis; Antirheumatic therapy; Tumour necrosis factor-alpha inhibitors; Acquired therapeutic resistance; Human anti-chimeric Ab; TUMOR-NECROSIS-FACTOR; CARDIAC TROPONIN-I; MONOCLONAL-ANTIBODY; CLINICAL-RESPONSE; TREATMENT FAILURE; CROHNS-DISEASE; THERAPY; METHOTREXATE; INTERFERENCES; METAANALYSIS;
D O I
10.1016/j.jbspin.2010.02.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Infliximab (IFX) can be immunogenic for humans and lead to the formation of antibodies against IFX (anti-IFX Ab), which could induce acquired IFX resistance. Objective: To test whether the presence of anti-IFX Ab and residual circulating IFX levels are associated with acquired IFX resistance in RA. Methods: A multivariate logistic regression was used to analyze the relationship between anti-IFX Ab, residual IFX concentrations, and acquired IFX resistance in a nested cohort within the Swiss RA registry (SCQM-RA). Results: Sixty-four RA patients on longstanding IFX therapy were included; 24 with an acquired therapeutic resistance to IFX and 40 with continuous good response to IFX. The two groups had similar disease characteristics, but patients with acquired IFX resistance required significantly higher dosage of IFX (5.4 mg/kg versus 4.3 mg/kg, p = 0.02) and shorter infusion intervals (7.1 versus 8.7 weeks, p = 0.01) than long-term good responders. The presence of residual IFX tended to be associated with a decreased risk of acquired therapeutic resistance (OR 0.4 [95% CI: 0.1 - 1.5]), while the presence of anti-IFX Ab tended to be associated with an increased risk of acquired therapeutic resistance (OR: 1.8 [95% CI: 0.4 - 9.0]). The presence of either high anti-IFX Ab levels or low residual IFX concentrations was strongly associated with acquired therapeutic resistance to IFX (OR 5.9, 95% CI 1.3 - 26.6). However, just 42% of patients with acquired IFX resistance had either low IFX or high anti-IFX Ab levels. Conclusion: These results suggest that the assessment of anti-IFX Ab and residual IFX levels is of limited value for individual patients in routine clinical care. (C) 2010 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:313 / 318
页数:6
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