TY - JOUR
T1 - Results of targeted anti-tumor necrosis factor therapy with etanercept (ENBREL) in patients with advanced heart failure
AU - Bozkurt, Biykem
AU - Torre, Guillermo
AU - Warren, Marshelle Smith
AU - Whitmore, James
AU - Soran, Ozlem Z.
AU - Feldman, Arthur M.
AU - Mann, Douglas L.
PY - 2001/2/27
Y1 - 2001/2/27
N2 - 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/m2 (n = 16) or 12 mg/m2 (n = 15) or with placebo (n = 16) for 3 months. Doses of 5 and 12 mg/m2 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.
AB - 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/m2 (n = 16) or 12 mg/m2 (n = 15) or with placebo (n = 16) for 3 months. Doses of 5 and 12 mg/m2 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.
KW - Cytokines
KW - Growth substances
KW - Heart failure
KW - Myocardial contraction
KW - Tumor necrosis factor
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U2 - 10.1161/01.CIR.103.8.1044
DO - 10.1161/01.CIR.103.8.1044
M3 - Article
C2 - 11222463
AN - SCOPUS:0035957036
SN - 0009-7322
VL - 103
SP - 1044
EP - 1047
JO - Circulation
JF - Circulation
IS - 8
ER -