A comparison of semiparametric approaches to evaluate composite endpoints in heart failure trials

Gerrit Toenges1, Tobias Mütze2, Antje Jahn-Eimermacher3

  • 1Institute of Medical Biostatistics, Epidemiology and Informatics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Insights

This study compares statistical models for heart failure (HF) trials. The Lin, Wei, Yang, and Ying (LWYY) model is most appropriate for composite endpoints, outperforming Cox and Mao-Lin models in analyzing recurrent events.

Area of Science:

  • Cardiovascular medicine
  • Biostatistics
  • Clinical trial methodology

Background:

  • Heart failure (HF) trials commonly use composite endpoints (cardiovascular death, HF hospitalizations) analyzed via time-to-first-event Cox models.
  • This approach overlooks recurrent events, potentially biasing treatment effect estimates.

Purpose of the Study:

  • To evaluate the performance of Cox, Lin, Wei, Yang, and Ying (LWYY), and Mao-Lin models for composite endpoints in HF trials.
  • To explain the behavior of composite treatment effect estimates using least false parameter theory and joint frailty models.

Main Methods:

  • Application of least false parameter theory to Cox, LWYY, and Mao-Lin models.
  • Utilizing joint frailty models to account for distinct treatment effects and correlated risks of cardiovascular death and HF hospitalizations.
  • Comparison with empirical data from the PARADIGM-HF trial.

Main Results:

  • Composite treatment effect estimates decrease with trial duration when treatment benefits both outcomes, due to outcome correlation.
  • The Cox model's estimates are more attenuated by this correlation compared to recurrent event models.
  • LWYY and Mao-Lin models show similar behavior, but LWYY is preferred due to better handling of mortality effects.

Conclusions:

  • The LWYY model is the most suitable for analyzing composite endpoints in HF trials.
  • Recurrent event models offer advantages over traditional Cox models by capturing more event data.
  • Understanding model behavior under different treatment effect scenarios is crucial for accurate HF trial interpretation.

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