Validity and Utility of a Hierarchical Composite End Point for Clinical Trials of Kidney Disease Progression: A Review

Author:

Little Dustin J.1ORCID,Gasparyan Samvel B.2ORCID,Schloemer Patrick3,Jongs Niels4ORCID,Brinker Meike5ORCID,Karpefors Martin2ORCID,Tasto Christoph5,Rethemeier Nicole5ORCID,Frison Lars2ORCID,Nkulikiyinka Richard3,Rossert Jerome1,Heerspink Hiddo J.L.46ORCID

Affiliation:

1. Late Stage Development, Cardiovascular, Renal and Metabolism (CVRM), Biopharmaceuticals R&D, AstraZeneca, Gaithersburg, Maryland

2. Late Stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden

3. Pharmaceuticals, Research and Development, Bayer AG, Berlin, Germany

4. Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands

5. Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany

6. The George Institute for Global Health, Sydney, New South Wales, Australia

Abstract

Clinical trials in nephrology often use composite end points comprising clinical events, such as onset of ESKD and initiation of kidney function replacement therapy, along with a sustained large (e.g., ≥50%) decrease in GFR. Such events typically occur late in the disease course, resulting in large trials in which most participants do not contribute clinical events. In addition, components of the end point are considered of equal importance; however, their clinical significance varies. For example, kidney function replacement therapy initiation is likely to be clinically more meaningful than GFR decline of ≥50%. By contrast, hierarchical composite end points (HCEs) combine multiple outcomes and prioritize each patient's most clinically relevant outcome for inclusion in analysis. In this review, we consider the use of HCEs in clinical trials of CKD progression, emphasizing the potential to combine dichotomous clinical events such as those typically used in CKD progression trials, with the continuous variable of GFR over time, while ranking all components according to clinical significance. We consider maraca plots to visualize overall treatment effects and the contributions of individual components, discuss the application of win odds in kidney HCE trials, and review general design considerations for clinical trials for CKD progression with kidney HCE as an efficacy end point.

Funder

AstraZeneca

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Nephrology,General Medicine

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