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Validity and Utility of a Hierarchical Composite End Point for Clinical Trials of Kidney Disease Progression: A Review.
Little, Dustin J; Gasparyan, Samvel B; Schloemer, Patrick; Jongs, Niels; Brinker, Meike; Karpefors, Martin; Tasto, Christoph; Rethemeier, Nicole; Frison, Lars; Nkulikiyinka, Richard; Rossert, Jerome; Heerspink, Hiddo J L.
Afiliação
  • Little DJ; Late Stage Development, Cardiovascular, Renal and Metabolism (CVRM), Biopharmaceuticals R&D, AstraZeneca, Gaithersburg, Maryland.
  • Gasparyan SB; Late Stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Schloemer P; Pharmaceuticals, Research and Development, Bayer AG, Berlin, Germany.
  • Jongs N; Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Brinker M; Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany.
  • Karpefors M; Late Stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Tasto C; Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany.
  • Rethemeier N; Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany.
  • Frison L; Late Stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Nkulikiyinka R; Pharmaceuticals, Research and Development, Bayer AG, Berlin, Germany.
  • Rossert J; Late Stage Development, Cardiovascular, Renal and Metabolism (CVRM), Biopharmaceuticals R&D, AstraZeneca, Gaithersburg, Maryland.
  • Heerspink HJL; Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
J Am Soc Nephrol ; 34(12): 1928-1935, 2023 12 01.
Article em En | MEDLINE | ID: mdl-37807165
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article