Evaluating treatment efficacy by multiple end points in phase II acute heart failure clinical trials: analyzing data using a global method

Circ Heart Fail. 2012 Nov;5(6):742-9. doi: 10.1161/CIRCHEARTFAILURE.112.969154. Epub 2012 Oct 11.

Abstract

Background: To assess concomitant simultaneous effects on multiple end points using global statistical methods in phase II acute heart failure studies.

Methods and results: Using simulations we have assessed different statistical methods to evaluate concomitant effects of a new intervention on dyspnea relief (using 2 measures), length of hospital stay, worsening heart failure to 5 days, mortality, and heart failure readmission to 30 days. Treatment effect scenarios included large (20% to 28% relative improvements) and very large (30% to 43% relative improvements) effects among others. Placebo responses and correlations among end points typical in recent acute heart failure clinical trials were used. Powers for the average Z score exceeded 70% with ≥75 patients per group for 35% relative improvement across all 6 end points. Assessing dyspnea alone generally provides lower power than the average Z score approach, with power deducted ≈50% under most of scenarios. Other approaches generally provide lower power than the average Z score method.

Conclusions: Assessing the effects of new therapies on multiple clinical end points using the average Z score enables detection of therapeutic efficacy using sample sizes of 100 to 150 patients per group, approximately double the power achievable assessing the effects on dyspnea alone.

Publication types

  • Evaluation Study

MeSH terms

  • Acute Disease
  • Clinical Trials, Phase II as Topic / standards*
  • Disease Management*
  • Dyspnea / prevention & control
  • Endpoint Determination*
  • Heart Failure / mortality
  • Heart Failure / therapy*
  • Hospital Mortality
  • Humans
  • Length of Stay
  • Patient Readmission
  • Statistics as Topic / methods*
  • Treatment Outcome