Design of a prospective patient-level pooled analysis of two parallel trials of empagliflozin in patients with established heart failure.


Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
12 2020
Historique:
received: 11 11 2020
revised: 20 11 2020
accepted: 25 11 2020
pubmed: 1 12 2020
medline: 14 5 2021
entrez: 30 11 2020
Statut: ppublish

Résumé

The EMPEROR-Reduced trial demonstrated that empagliflozin reduced the combined risk of cardiovascular death or hospitalization for heart failure in patients with a reduced ejection fraction, and the EMPEROR-Preserved trial is currently evaluating the effect of the drug on the same endpoint in patients with an ejection fraction >40%. However, neither the trial was designed to have adequate statistical power to evaluate the effects of empagliflozin and dapagliflozin on major adverse renal outcomes or on mortality. Herein we describe the design of a prospective individual patient-level pooled analysis of two large-scale trials with empagliflozin (EMPEROR-Reduced and EMPEROR-Preserved) in patients with heart failure across the spectrum of ejection fraction. The trials were carried out in parallel using the same administrative structure and committees, randomization procedure, schedule of study visits and adjudication criteria and similar groups of investigators and case report forms. The two component trials specified the same primary and key secondary endpoints and used an identical hierarchical testing procedure, which included a pooled analysis of the two trials as a key component of the hierarchy. Consequently, the pooled analysis has been prospectively assigned a false positive error rate, which is conditional on one or both trials first achieving success on their primary and one or both key secondary endpoints. The pooled analysis has its own statistical plan with its own endpoints, and this plan was finalized before either trial had begun recruitment of patients into either study. The primary endpoint of the pooled analysis is a composite of serious adverse renal outcomes, defined by chronic dialysis, renal transplantation and a profound or sustained decrease in glomerular filtration rate. All-cause and cardiovascular mortality are specified as secondary endpoints. The planned pooled analysis has an unusually high degree of statistical rigour that will allow it to address important questions that cannot be fully addressed by the individual trials.

Identifiants

pubmed: 33251659
doi: 10.1002/ejhf.2065
pmc: PMC7898542
doi:

Substances chimiques

Benzhydryl Compounds 0
Cardiovascular Agents 0
Glucosides 0
Sodium-Glucose Transporter 2 Inhibitors 0
empagliflozin HDC1R2M35U

Types de publication

Journal Article Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

2393-2398

Informations de copyright

© 2020 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

Eur J Heart Fail. 2019 Oct;21(10):1279-1287
pubmed: 31523904
Lancet. 2019 Jan 5;393(10166):31-39
pubmed: 30424892
Lancet Diabetes Endocrinol. 2019 Nov;7(11):845-854
pubmed: 31495651
N Engl J Med. 2020 Oct 8;383(15):1413-1424
pubmed: 32865377
Am J Kidney Dis. 2021 Feb;77(2):280-286
pubmed: 32711072
N Engl J Med. 2019 Jun 13;380(24):2295-2306
pubmed: 30990260
Stat Med. 2012 Dec 20;31(29):3840-57
pubmed: 22786621
N Engl J Med. 2021 Jan 14;384(2):117-128
pubmed: 33200892
Eur J Heart Fail. 2019 Oct;21(10):1270-1278
pubmed: 31584231
Eur Heart J. 2020 Sep 21;41(36):3398-3401
pubmed: 32935133
Eur J Heart Fail. 2020 Nov;22(11):1987-1990
pubmed: 32946169
N Engl J Med. 2016 Jul 28;375(4):323-34
pubmed: 27299675
N Engl J Med. 2020 Oct 8;383(15):1436-1446
pubmed: 32970396
N Engl J Med. 2017 Aug 17;377(7):644-657
pubmed: 28605608
Lancet Diabetes Endocrinol. 2019 Aug;7(8):606-617
pubmed: 31196815
Lancet. 2020 Sep 19;396(10254):819-829
pubmed: 32877652
J Am Soc Nephrol. 2020 May;31(5):907-919
pubmed: 32276962
N Engl J Med. 2019 Nov 21;381(21):1995-2008
pubmed: 31535829
Circulation. 2021 Jan 26;143(4):298-309
pubmed: 33040613

Auteurs

Milton Packer (M)

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX, USA.
Imperial College, London, UK.

Javed Butler (J)

Department of Medicine, University of Mississippi School of Medicine, Jackson, MS, USA.

Gerasimos Filippatos (G)

National and Kapodistrian University of Athens School of Medicine, Athens University Hospital Attikon, Athens, Greece.

Faiez Zannad (F)

Université de Lorraine, Inserm INI-CRCT, CHRU, Nancy, France.

Joao Pedro Ferreira (JP)

Université de Lorraine, Inserm INI-CRCT, CHRU, Nancy, France.

Cordula Zeller (C)

Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany.

Martina Brueckmann (M)

Boehringer Ingelheim International GmbH and Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany.

Waheed Jamal (W)

Boehringer Ingelheim International GmbH, Ingelheim, Germany.

Stuart J Pocock (SJ)

Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK.

Stefan D Anker (SD)

Department of Cardiology (CVK), and Berlin Institute of Health Center for Regenerative Therapies, German Centre for Cardiovascular Research Partner Site Berlin, Charité Universitätsmedizin, Berlin, Germany.

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Classifications MeSH