TY - JOUR
T1 - Clinical Outcome Predictions for the VerICiguaT Global Study in Subjects With Heart Failure With Reduced Ejection Fraction (VICTORIA) Trial
AU - VICTORIA Study Group
AU - Mentz, Robert J.
AU - Mulder, Hillary
AU - Mosterd, Arend
AU - Sweitzer, Nancy K.
AU - senni, Michele
AU - Butler, Javed
AU - Ezekowitz, Justin A.
AU - Lam, Carolyn S.P.
AU - Pieske, Burkert
AU - Ponikowski, Piotr
AU - Voors, Adriaan A.
AU - Anstrom, Kevin J.
AU - Armstrong, Paul W.
AU - O'connor, Christopher M.
AU - Hernandez, Adrian F.
N1 - Funding Information: The VICTORIA trial was funded by Merck Sharp & Dohme Corp. a subsidiary of Merck & Co. Inc. Kenilworth, NJ, USA, and Bayer. Dr Mentz reports research support and honoraria from Bayer and Merck Sharp & Dohme Corp. a subsidiary of Merck & Co. Inc. Kenilworth, NJ. Hillary Mulder has nothing to report. Dr Mosterd has nothing to report. Dr Sweitzer reports consulting fees from Merck. Dr. Senni has nothing to report. Dr Butler reports consulting fees from Bayer, Merck, Amgen, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, CVRx, G3 Pharmaceutical, Janssen, Luitpold, Medtronic, Novartis, Vifor, and Novo Nordisk. Justin Ezekowitz reports research grants from Bayer, Merck, Servier, Amgen Sanofi, Novartis, Cytokinetics, American Regent, and Applied Therapeutics; consulting fees from Bayer, Merck, Servier, Amgen, Sanofi, Novartis, Cytokinetics, American Regent, and Applied Therapeutics. Dr Lam reports research grants from Bayer, National Medical Research Council of Singapore, Boston Scientific, Roche Diagnostic, Medtronic, Vifor Pharma, and AstraZeneca; consulting fees from Merck, Bayer, Boston Scientific, Roche Diagnostic, Vifor Pharma, AstraZeneca, Novartis, Amgen, Janssen Research & Development LLC, Menarini, Boehringer Ingelheim, Abbott Diagnostics, Corvia, Stealth BioTherapeutics, Novo Nordisk, JanaCare, Biofourmis, Darma, Applied Therapeutics, MyoKardia, Cytokinetics, WebMD Global LLC, Radcliffe Group Ltd, and Corpus. In addition, Dr Lam has a patent PCT/SG2016/050217 pending, and a patent 16/216,929 pending and Co-founder & nonexecutive director of eKo.ai. Dr Pieske reports research grants from MSD, Bayer, and Servier; consulting fees from MSD, Bayer, Servier, Bristol-Myers Squibb, MedScape, Daiichi-Sankyo, and Novartis; nonfinancial support from MSD, Bayer, and Novartis. Dr Ponikowski reports research grants from Vifor Pharma Ltd, and Servier; has received consulting fees from MSD, Novartis, Vifor Pharma Ltd, Servier, Bristol-Myers Squibb, Boehringer Ingelheim, Respicardia, AstraZeneca, Cibiem, RenalGuardSolution, and Berlin Chemie. Dr Voors reports honoraria from Bayer and Merck. Dr Anstrom reports research grants from MSD and NIH. Dr Armstrong reports research grants from Merck, Bayer, Sanofi-aventis Recherche & Développement, Boehringer Ingelheim, and CSL Limited; consulting fees from Merck, Bayer, AstraZeneca, and Novartis. Dr O'Connor reports research funding from Merck; consulting fees from Bayer, Dey LP, and Bristol-Myers Squibb Foundation. Dr Hernandez reports research grants from Merck, AstraZeneca, Novartis, and Verily; consulting fees from Merck, Bayer, Amgen, AstraZeneca, and Novartis. The VICTORIA trial was funded by Merck Sharp & Dohme Corp. a subsidiary of Merck & Co. Inc. Kenilworth, NJ, USA and Bayer AG, Wuppertal, Germany. Funding Information: The VICTORIA trial was funded by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA, and Bayer. Funding Information: The VICTORIA trial was funded by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA and Bayer AG, Wuppertal, Germany. Publisher Copyright: © 2021 Elsevier Inc.
PY - 2021/9
Y1 - 2021/9
N2 - Background: The prediction of outcomes in patients with heart failure (HF) may inform prognosis, clinical decisions regarding treatment selection, and new trial planning. The VerICiguaT Global Study in Subjects With Heart Failure With Reduced Ejection Fraction included high-risk patients with HF with reduced ejection fraction and a recent worsening HF event. The study participants had a high event rate despite the use of contemporary guideline-based therapies. To provide generalizable predictive data for a broad population with a recent worsening HF event, we focused on risk prognostication in the placebo group. Methods and Results: Data from 2524 participants randomized to placebo with chronic HF (New York Heart Association functional class II–IV) and an ejection fraction of less than 45% were studied and backward variable selection was used to create Cox proportional hazards models for clinical end points, selecting from 66 candidate predictors. Final model results were produced, accounting for missing data, and nonlinearities. Optimism-corrected c-indices were calculated using 200 bootstrap samples. Over a median follow-up of 10.4 months, the primary outcome of HF hospitalization or cardiovascular death occurred in 972 patients (38.5%). Independent predictors of increased risk for the primary end point included HF characteristics (longer HF duration and worse New York Heart Association functional class), medical history (prior myocardial infarction), and laboratory values (higher N-terminal pro-hormone B-type natriuretic peptide, bilirubin, urate; lower chloride and albumin). Optimism-corrected c-indices were 0.68 for the HF hospitalization/cardiovascular death model, 0.68 for HF hospitalization/all-cause death, 0.72 for cardiovascular death, and 0.73 for all-cause death. Conclusions: Predictive models developed in a large diverse clinical trial with comprehensive clinical and laboratory baseline data—including novel measures—performed well in high-risk patients with HF who were receiving excellent guideline-based clinical care.Clinical Trial Registration: Clinicaltrials.gov identifier, NCT02861534.Lay Summary: Patients with heart failure may benefit from tools that help clinicians to better understand a patient's risk for future events like hospitalization. Relatively few risk models have been created after the worsening of heart failure in a contemporary cohort. We provide insights on the risk factors for clinical events from a recent, large, global trial of patients with worsening heart failure to help clinicians better understand and communicate prognosis and select treatment options.
AB - Background: The prediction of outcomes in patients with heart failure (HF) may inform prognosis, clinical decisions regarding treatment selection, and new trial planning. The VerICiguaT Global Study in Subjects With Heart Failure With Reduced Ejection Fraction included high-risk patients with HF with reduced ejection fraction and a recent worsening HF event. The study participants had a high event rate despite the use of contemporary guideline-based therapies. To provide generalizable predictive data for a broad population with a recent worsening HF event, we focused on risk prognostication in the placebo group. Methods and Results: Data from 2524 participants randomized to placebo with chronic HF (New York Heart Association functional class II–IV) and an ejection fraction of less than 45% were studied and backward variable selection was used to create Cox proportional hazards models for clinical end points, selecting from 66 candidate predictors. Final model results were produced, accounting for missing data, and nonlinearities. Optimism-corrected c-indices were calculated using 200 bootstrap samples. Over a median follow-up of 10.4 months, the primary outcome of HF hospitalization or cardiovascular death occurred in 972 patients (38.5%). Independent predictors of increased risk for the primary end point included HF characteristics (longer HF duration and worse New York Heart Association functional class), medical history (prior myocardial infarction), and laboratory values (higher N-terminal pro-hormone B-type natriuretic peptide, bilirubin, urate; lower chloride and albumin). Optimism-corrected c-indices were 0.68 for the HF hospitalization/cardiovascular death model, 0.68 for HF hospitalization/all-cause death, 0.72 for cardiovascular death, and 0.73 for all-cause death. Conclusions: Predictive models developed in a large diverse clinical trial with comprehensive clinical and laboratory baseline data—including novel measures—performed well in high-risk patients with HF who were receiving excellent guideline-based clinical care.Clinical Trial Registration: Clinicaltrials.gov identifier, NCT02861534.Lay Summary: Patients with heart failure may benefit from tools that help clinicians to better understand a patient's risk for future events like hospitalization. Relatively few risk models have been created after the worsening of heart failure in a contemporary cohort. We provide insights on the risk factors for clinical events from a recent, large, global trial of patients with worsening heart failure to help clinicians better understand and communicate prognosis and select treatment options.
KW - Heart failure with reduced ejection fraction
KW - outcomes
KW - predictive models
KW - prognosis
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U2 - 10.1016/j.cardfail.2021.05.016
DO - 10.1016/j.cardfail.2021.05.016
M3 - Article
C2 - 34217593
SN - 1071-9164
VL - 27
SP - 949
EP - 956
JO - Journal of cardiac failure
JF - Journal of cardiac failure
IS - 9
ER -