The win ratio approach for composite endpoints: practical guidance based on previous experience

Author:

Redfors Björn123ORCID,Gregson John4ORCID,Crowley Aaron1ORCID,McAndrew Thomas1ORCID,Ben-Yehuda Ori12,Stone Gregg W15ORCID,Pocock Stuart J4

Affiliation:

1. Clinical Trials Center, Cardiovascular Research Foundation, New York, NY, USA

2. Division of Cardiology, NewYork-Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY, USA

3. Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden

4. Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London WC1E7HT, UK

5. The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA

Abstract

Abstract The win ratio was introduced in 2012 as a new method for examining composite endpoints and has since been widely adopted in cardiovascular (CV) trials. Improving upon conventional methods for analysing composite endpoints, the win ratio accounts for relative priorities of the components and allows the components to be different types of outcomes. For example, the win ratio can combine the time to death with the number of occurrences of a non-fatal outcome such as CV-related hospitalizations (CVHs) in a single hierarchical composite endpoint. The win ratio can provide greater statistical power to detect and quantify a treatment difference by using all available information contained in the component outcomes. The win ratio can also incorporate quantitative outcomes such as exercise tests or quality-of-life scores. There is a need for more practical guidance on how best to design trials using the win ratio approach. This manuscript provides an overview of the principles behind the win ratio and provides insights into how to implement the win ratio in CV trial design and reporting, including how to determine trial size.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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