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Comparative efficacy of vericiguat to sacubitril/valsartan for patients with heart failure reduced ejection fraction: Systematic review and network meta-analysis.
Kang, Dong-Won; Kang, Seung-Ho; Lee, Kyungmin; Nam, Kyungae; Kim, Eui-Soon; Yoon, Jong-Chan; Park, Sun-Kyeong.
Affiliation
  • Kang DW; Division of Outcomes Research and Quality, Department of Surgery, Penn State College of Medicine, Hershey, PA, United States of America.
  • Kang SH; Department of Statistics and Data Science, Yonsei University, Seoul, Republic of Korea.
  • Lee K; Market Access & Policy Advocacy, Bayer Korea, Seoul, Republic of Korea; Institute of Regulatory Innovation through Science, Department of Regulatory Science, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
  • Nam K; College of Pharmacy, The Catholic University of Korea, Bucheon-si, Gyeonggi-do, Republic of Korea.
  • Kim ES; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.
  • Yoon JC; Division of Cardiology, Department of Internal Medicine, Seoul St. Mary's Hospital, Catholic Research Institute for Intractable Cardiovascular Disease, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Park SK; College of Pharmacy, The Catholic University of Korea, Bucheon-si, Gyeonggi-do, Republic of Korea. Electronic address: sk.park@catholic.ac.kr.
Int J Cardiol ; 400: 131786, 2024 Apr 01.
Article in En | MEDLINE | ID: mdl-38242507
ABSTRACT

BACKGROUND:

Despite the established efficacy of vericiguat compared to placebo, uncertainties remain regarding its comparative efficacy to sacubitril/valsartan for patients with heart failure reduced ejection fraction (HFrEF). This study aimed to assess the relative efficacy of vericiguat and sacubitril/valsartan through a systematic review, network meta-analysis, and non-inferiority tests.

METHODS:

A systematic review was conducted to identify the randomized phase 3 clinical trials involving vericiguat and sacubitril/valsartan. The hazard ratios (HRs) with 95% confidence intervals (CI) for cardiovascular death (CVD) and hospitalization due to HF (hHF) were extracted from these trials and synthesized via network meta-analysis. Non-inferiority testing of vericiguat was performed using a fixed-margin method with a predefined non-inferiority margin (1.24). Sensitivity analyses explored the impact of the time from hHF to screening.

RESULTS:

Among the 1366 studies, two trials (VICTORIA and PARADIGM-HF) met the inclusion criteria. Network meta-analysis demonstrated that the HR for CVD or hHF with vericiguat did not significantly differ from that for sacubitril/valsartan (HR 0.88, 95% CI0.62-1.23). The upper limit of the 95% CI was less than the predefined margin of 1.24, confirming vericiguat's non-inferiority to sacubitril/valsartan. Sensitivity analyses affirmed the robustness of the base-case results.

CONCLUSION:

Vericiguat exhibited a comparable risk of CVD or hHF when contrasted with sacubitril/valsartan. Importantly, in patients with HFrEF, vericiguat's efficacy was not statistically inferior to that of sacubitril/valsartan. These findings reinforce the potential of vericiguat as a viable treatment option for this patient population.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stroke Volume / Tetrazoles / Biphenyl Compounds / Drug Combinations / Angiotensin Receptor Antagonists / Valsartan / Network Meta-Analysis / Aminobutyrates / Heart Failure Type of study: Clinical_trials / Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Int J Cardiol / Int. j. cardiol / International journal of cardiology Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stroke Volume / Tetrazoles / Biphenyl Compounds / Drug Combinations / Angiotensin Receptor Antagonists / Valsartan / Network Meta-Analysis / Aminobutyrates / Heart Failure Type of study: Clinical_trials / Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Int J Cardiol / Int. j. cardiol / International journal of cardiology Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Países Bajos