TY - JOUR
T1 - Effect of Ejection Fraction on Clinical Outcomes in Patients Treated With Omecamtiv Mecarbil in GALACTIC-HF
AU - Teerlink, John R.
AU - Diaz, Rafael
AU - Felker, G. Michael
AU - McMurray, John J.
AU - Metra, Marco
AU - Solomon, Scott D.
AU - Biering-Sorensen, Tor
AU - Boehm, Michael
AU - Bonderman, Diana
AU - Fang, James C.
AU - Lanfear, David E.
AU - Lund, Mayanna
AU - Momomura, Shin-Ichi
AU - O'Meara, Eileen
AU - Ponikowski, Piotr
AU - Spinar, Jindrich
AU - Flores-Arredondo, Jose H.
AU - Claggett, Brian L.
AU - Heitner, Stephen B.
AU - Kupfer, Stuart
AU - Abbasi, Siddique A.
AU - Malik, Fady
AU - GALACTIC HF Investigators
PY - 2021
Y1 - 2021
N2 - BACKGROUND In GALACTIC-HF (Global Approach to Lowering Adverse Cardiac outcomes Through Improving Contractility in Heart Failure) (n = 8,256), the cardiac myosin activator, omecamtiv mecarbil, significantly reduced the primary composite endpoint (PCE) of time-to-first heart failure event or cardiovascular death in patients with heart failure and reduced ejection fraction (EF) (OBJECTIVES The purpose of this study was to evaluate the influence of baseline EF on the therapeutic effect of omecamtiv mecarbil.METHODS Outcomes in patients treated with omecamtiv mecarbil were compared with placebo according to EF.RESULTS The risk of the PCE in the placebo group was nearly 1.8-fold greater in the lowest EF (= 33%) quartile. Amongst the pre-specified subgroups, EF was the strongest modifier of the treatment effect of omecamtiv mecarbil on the PCE (interaction as continuous variable, p = 0.004). Patients receiving omecamtiv mecarbil had a progressively greater relative and absolute treatment effect as baseline EF decreased, with a 17% relative risk reduction for the PCE in patients with baseline EF = 33% (n =1,750; hazard ratio: 0.99; 95% confidence interval: 0.84 to 1.16; interaction as EF by quartiles, p = 0.013). The absolute reduction in the PCE increased with decreasing EF (EFCONCLUSIONS In heart failure patients with reduced EF, omecamtiv mecarbil produced greater therapeutic benefit as baseline EF decreased. These findings are consistent with the drug's mechanism of selectively improving systolic function and presents an important opportunity to improve the outcomes in a group of patients at greatest risk. Published by Elsevier on behalf of the American College of Cardiology Foundation.
AB - BACKGROUND In GALACTIC-HF (Global Approach to Lowering Adverse Cardiac outcomes Through Improving Contractility in Heart Failure) (n = 8,256), the cardiac myosin activator, omecamtiv mecarbil, significantly reduced the primary composite endpoint (PCE) of time-to-first heart failure event or cardiovascular death in patients with heart failure and reduced ejection fraction (EF) (OBJECTIVES The purpose of this study was to evaluate the influence of baseline EF on the therapeutic effect of omecamtiv mecarbil.METHODS Outcomes in patients treated with omecamtiv mecarbil were compared with placebo according to EF.RESULTS The risk of the PCE in the placebo group was nearly 1.8-fold greater in the lowest EF (= 33%) quartile. Amongst the pre-specified subgroups, EF was the strongest modifier of the treatment effect of omecamtiv mecarbil on the PCE (interaction as continuous variable, p = 0.004). Patients receiving omecamtiv mecarbil had a progressively greater relative and absolute treatment effect as baseline EF decreased, with a 17% relative risk reduction for the PCE in patients with baseline EF = 33% (n =1,750; hazard ratio: 0.99; 95% confidence interval: 0.84 to 1.16; interaction as EF by quartiles, p = 0.013). The absolute reduction in the PCE increased with decreasing EF (EFCONCLUSIONS In heart failure patients with reduced EF, omecamtiv mecarbil produced greater therapeutic benefit as baseline EF decreased. These findings are consistent with the drug's mechanism of selectively improving systolic function and presents an important opportunity to improve the outcomes in a group of patients at greatest risk. Published by Elsevier on behalf of the American College of Cardiology Foundation.
KW - cardiovascular outcomes trial
KW - heart failure with reduced ejection fraction
KW - myotrope
KW - CARDIAC MYOSIN ACTIVATOR
KW - HEART-FAILURE
KW - INCREASE CONTRACTILITY
KW - DOUBLE-BLIND
KW - PHASE-2
U2 - 10.1016/j.jacc.2021.04.065
DO - 10.1016/j.jacc.2021.04.065
M3 - Journal article
C2 - 34015475
VL - 78
SP - 97
EP - 108
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
SN - 0735-1097
IS - 2
ER -