Results of targeted anti-tumor necrosis factor therapy with etanercept (ENBREL) in patients with advanced heart failure

被引:310
作者
Bozkurt, B
Torre-Amione, G
Warren, MS
Whitmore, J
Soran, OZ
Feldman, AM
Mann, DL
机构
[1] Houston VA Med Ctr, Winters Ctr Heart Failure Res 151C, Dept Med, Houston, TX 77030 USA
[2] Baylor Coll Med, Houston, TX 77030 USA
[3] Univ Pittsburgh, Med Ctr Hlth Syst, Cardiovasc Inst, Pittsburgh, PA USA
[4] Methodist Hosp, Houston, TX 77030 USA
[5] Immunex Corp, Seattle, WA USA
关键词
heart failure; myocardial contraction; growth substances; cytokines; tumor necrosis factor;
D O I
10.1161/01.CIR.103.8.1044
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Previously, we showed that tumor necrosis factor (TNF) antagonism with etanercept, a soluble TNF receptor, was well tolerated and that it suppressed circulating levels of biologically active TNF for 14 days in patients with moderate heart failure. However, the effects of sustained TNF antagonism in heart failure are not known. Methods and Results-We conducted a randomized, double-blind, placebo-controlled, multidose trial of etanercept in 47 patients with NYHA class III to IV heart failure. Patients were treated with biweekly subcutaneous injections of etanercept 5 mg/m(2) (n=16) or 12 mg/m(2) (n=15) or with placebo (n=16) for 3 months. Doses of 5 and 12 mg/m(2) etanercept were safe and well tolerated for 3 months. Treatment with etanercept led to a significant dose-dependent improvement in left ventricular (LV) ejection fraction and LV remodeling, and there was a trend toward an improvement in patient functional status, as determined by clinical composite score. Conclusion-Treatment with etanercept for 3 months was safe and well-tolerated in patients with advanced heart failure, and it resulted in a significant dose-dependent improvement in LV structure and function and a trend toward improvement in patient functional status.
引用
收藏
页码:1044 / 1047
页数:4
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