Institute of Life Sciences, Scuola Superiore Sant'Anna, Piazza Martiri della Libertà 33, 56124, Pisa, Italy.
Cardiology Division, University Hospital of Pisa, Piazza Martiri della Libertà 33, 56124, Pisa, Italy.
Cardiovasc Drugs Ther. 2021 Oct;35(5):1067-1076. doi: 10.1007/s10557-020-07099-2. Epub 2020 Oct 19.
Sacubitril/valsartan, vericiguat, and the sodium-glucose co-transporter-2 inhibitors (SGLT2i) dapagliflozin and empagliflozin proved effective in phase 3 trials on heart failure with reduced ejection fraction (HFrEF).
We compared the treatment arms (sacubitril/valsartan, vericiguat, and SGLT2i) with the respective control arms (standard-of-care [SOC]) through a network meta-analysis of the phase 3 trials (PARADIGM-HF, VICTORIA, DAPA-HF, EMPEROR-Reduced), a phase 2 trial on vericiguat and the HFrEF subgroup of DECLARE-TIMI 58.
There was a trend towards decreased risk of cardiovascular (CV) death or HF hospitalization with SGLT2i than sacubitril/valsartan (HR 0.92, 95% CI 0.81 to 1.05) and vericiguat (HR 0.83, 95% CI 0.73 to 0.94). A non-significant effect of SGLT2i on CV mortality compared to sacubitril/valsartan (HR 1.04, 95% CI 0.88 to 1.24) and vericiguat (HR 0.88, 95% CI 0.63 to 1.22) was found. SGLT2i demonstrated the greatest effect on HF hospitalization (HR 0.69, 95% CI 0.62 to 0.77) over the SOC, as well as a significant benefit over vericiguat (HR 0.77, 95% CI 0.66 to 0.89), but not over sacubitril/valsartan (HR 0.87, 95% CI 0.75 to 1.02). SGLT2i were ranked as the most effective therapy, followed by sacubitril/valsartan and vericiguat.
Based on an indirect comparison, SGLT2i therapy is not associated with a significantly lower risk of CV death or HF hospitalization or CV death alone compared to sacubitril/valsartan or vericiguat. The risk of HF hospitalization does not differ significantly between patients on SGLT2i or sacubitril/valsartan, while dapagliflozin is superior to vericiguat.
PROSPERO ID 186351.
沙库巴曲缬沙坦、维立西呱以及钠-葡萄糖协同转运蛋白 2 抑制剂(SGLT2i)达格列净和恩格列净在射血分数降低的心力衰竭(HFrEF)的 3 期试验中均显示出疗效。
我们通过 3 期试验(PARADIGM-HF、VICTORIA、DAPA-HF、EMPEROR-Reduced)、维立西呱的 2 期试验以及 DECLARE-TIMI 58 的 HFrEF 亚组,对沙库巴曲缬沙坦、维立西呱和 SGLT2i 治疗组与各自的标准治疗(SOC)对照组进行了网络荟萃分析。
与沙库巴曲缬沙坦(HR 0.92,95%CI 0.81 至 1.05)和维立西呱(HR 0.83,95%CI 0.73 至 0.94)相比,SGLT2i 降低了心血管(CV)死亡或心力衰竭住院的风险趋势。与沙库巴曲缬沙坦(HR 1.04,95%CI 0.88 至 1.24)和维立西呱(HR 0.88,95%CI 0.63 至 1.22)相比,SGLT2i 对 CV 死亡率的影响无统计学意义。SGLT2i 对 SOC 组的心力衰竭住院(HR 0.69,95%CI 0.62 至 0.77)具有最大的影响,与维立西呱相比具有显著的获益(HR 0.77,95%CI 0.66 至 0.89),但与沙库巴曲缬沙坦相比则无获益(HR 0.87,95%CI 0.75 至 1.02)。SGLT2i 被列为最有效的治疗方法,其次是沙库巴曲缬沙坦和维立西呱。
基于间接比较,与沙库巴曲缬沙坦或维立西呱相比,SGLT2i 治疗并未显著降低 CV 死亡或心力衰竭住院或 CV 死亡的风险。与 SGLT2i 或沙库巴曲缬沙坦相比,心力衰竭住院的风险无显著差异,而达格列净优于维立西呱。
PROSPERO ID 186351。